Controlling intensity of a particle beam

Information

  • Patent Grant
  • 9723705
  • Patent Number
    9,723,705
  • Date Filed
    Friday, September 27, 2013
    10 years ago
  • Date Issued
    Tuesday, August 1, 2017
    6 years ago
Abstract
In an example, a synchrocyclotron includes a particle source to provide pulses of ionized plasma to a cavity; a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column outwardly; and an extraction channel to receive a beam of particles from the cavity for output from the particle accelerator. The particle source is configured to control pulse widths of the ionized plasma in order to control an intensity of the beam of particles. This example synchrocyclotron may include one or more of the following features, either alone or in combination.
Description
TECHNICAL FIELD

This disclosure relates generally to controlling the intensity of a particle beam, such as a proton or ion beam used in a particle therapy system.


BACKGROUND

Particle therapy systems use an accelerator to generate a particle beam for treating afflictions, such as tumors. In operation, the particle beam is accelerated inside a cavity of the particle accelerator, and removed from the cavity through an extraction channel. Various elements are used to focus the particle beam and apply it to appropriate areas of a patent.


Different patients may require different doses and dose rates of particles. The dose and dose rate applied to a patient is a function of the intensity of the particle beam. Controlling the intensity of the particle beam therefore enables control over the dose and dose rate.


SUMMARY

In an example, a synchrocyclotron includes a particle source to provide pulses of ionized plasma to a cavity; a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column outwardly; and an extraction channel to receive a beam of particles from the cavity for output from the particle accelerator. The particle source is configured to control pulse widths of the ionized plasma in order to control an intensity of the beam of particles. This example synchrocyclotron may include one or more of the following features, either alone or in combination.


The particle source may be configured to activate for a period of time in response to control signal, where the particle source generates a pulse of ionized plasma when activated. The particle source may be configured to generate pulses of ionized plasma periodically. The particle beam may be output for a duration of about 0.1 μs to 100 μs (e.g., 1 μs to 10 μs). The particle beam may be output for a duration of about 0.1 μs to 100 μs (e.g., 1 μs to 10 μs) about every 2 ms. The particle source may include cathodes to provide voltage to ionize hydrogen to produce the ionized plasma. The cathodes may be unheated by an external source.


In an example, a proton therapy system includes the foregoing synchrocyclotron, and a gantry on which the synchrocyclotron is mounted, where the gantry is rotatable relative to a patient position. Protons are output essentially directly from the synchrocyclotron to the patient position.


In an example, a synchrocyclotron includes a particle source to provide pulses of ionized plasma to a cavity, where the particle source includes cathodes to provide voltage to ionize hydrogen to produce the ionized plasma; a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column outwardly; and an extraction channel to receive a beam of particles from the cavity for output from the particle accelerator. A voltage associated with the cathodes is controllable in order to control an intensity of the beam of particles. This example synchrocyclotron may include one or more of the following features, either alone or in combination.


The cathodes may be unheated by an external source. The voltage may be controllable such that increasing the voltage increases an intensity of the beam of particles and such that decreasing the voltage decreases the intensity of the beam of particles.


In an example, a proton therapy system includes the foregoing synchrocyclotron, and a gantry on which the synchrocyclotron is mounted. The gantry is rotatable relative to a patient position. Protons are output essentially directly from the synchrocyclotron to the patient position.


In an example, a synchrocyclotron includes a particle source to provide pulses of ionized plasma to a cavity, where the particle source includes cathodes to provide voltage to ionize hydrogen to produce the ionized plasma; a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column outwardly; and an extraction channel to receive a beam of particles from the cavity for output from the particle accelerator. The particle source is controllable to adjust an amount of the hydrogen between the cathodes in order to control an intensity of the beam of particles. This example synchrocyclotron may include one or more of the following features, either alone or in combination.


The cathodes may be unheated by an external source. The amount of hydrogen may be adjustable such that increasing the amount of hydrogen increases an intensity of the beam of particles and such that decreasing the amount of hydrogen decreases the intensity of the beam of particles.


In an example, a proton therapy system includes the foregoing synchrocyclotron, and a gantry on which the synchrocyclotron is mounted. The gantry is rotatable relative to a patient position. Protons are output essentially directly from the synchrocyclotron to the patient position.


In an example, a synchrocyclotron includes a particle source to provide pulses of ionized plasma to a cavity; a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column outwardly; and an extraction channel to receive a beam of particles from the cavity for output from the particle accelerator. The voltage source is controllable to control the RF voltage rate in order to control an intensity of the beam of particles. This example synchrocyclotron may include one or more of the following features, either alone or in combination.


The particle source may include cathodes to provide voltage to ionize hydrogen to produce the ionized plasma, where the cathodes are unheated by an external source. A magnitude of the RF voltage may be adjustable such that increasing the magnitude increases an intensity of the beam of particles and such that decreasing the magnitude decreases the intensity of the beam of particles.


In an example, a proton therapy system includes the foregoing synchrocyclotron, and a gantry on which the synchrocyclotron is mounted. The gantry is rotatable relative to a patient position. Protons are output essentially directly from the synchrocyclotron to the patient position.


In an example, a synchrocyclotron includes a particle source to provide pulses of ionized plasma to a cavity; a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column outwardly, where the RF voltage sweeps between a maximum frequency and a minimum frequency; and an extraction channel to receive a beam of particles from the cavity for output from the particle accelerator. The particle source is controllable to provide pulses of the ionized plasma at specific frequencies proximate to a decrease from the maximum frequency of the RF voltage to the minimum frequency of the RF voltage. This example synchrocyclotron may include one or more of the following features, either alone or in combination.


The particle accelerator may be controllable to provide pulses of the ionized plasma between 132 MHz of RF voltage and 131 MHz of RF voltage from a decrease from a maximum frequency of about 135 MHz of the RF voltage. The particle source may include cathodes to provide voltage to ionize hydrogen to produce the ionized plasma. The cathodes may be unheated by an external source.


In an example, a proton therapy system includes the foregoing synchrocyclotron, and a gantry on which the synchrocyclotron is mounted. The gantry is rotatable relative to a patient position. Protons are output essentially directly from the synchrocyclotron to the patient position.


In an example, a synchrocyclotron includes a particle source to provide pulses of ionized plasma to a cavity; a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column outwardly; and an extraction channel to receive a beam of particles from the cavity for output from the particle accelerator. The particle source is configured to selectively output pulses of the ionized plasma in order to control an intensity of the beam of particles. This example synchrocyclotron may include one or more of the following features, either alone or in combination.


The RF voltage may sweep periodically from a maximum frequency to a minimum frequency. Selectively outputting the pulses may include outputting pulses in certain ones of the RF voltage sweeps and not in others of the RF voltage sweeps. Selectively outputting the pulses may include skipping pulse output in every Nth (N>1) sweep.


The synchrocyclotron may include a controller for performing operations that include: determining the intensity of the beam of particles; and selectively outputting the pulses based on the determined intensity.


In an example, a proton therapy system includes the foregoing synchrocyclotron, and a gantry on which the synchrocyclotron is mounted. The gantry is rotatable relative to a patient position. Protons are output essentially directly from the synchrocyclotron to the patient position.


In an example, a synchrocyclotron includes a particle source to provide pulses of ionized plasma to a cavity; a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column outwardly; and an extraction channel to receive a beam of particles from the cavity for output from the particle accelerator. The voltage source is configurable to vary a slope of the RF voltage in order to control an intensity of the beam of particles.


In an example, a proton therapy system includes the foregoing synchrocyclotron, and a gantry on which the synchrocyclotron is mounted. The gantry is rotatable relative to a patient position. Protons are output essentially directly from the synchrocyclotron to the patient position.


In an example, a synchrocyclotron includes a particle source to provide pulses of ionized plasma to a cavity; a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column outwardly, where the voltage source includes a first dee and a second dee, and where at least one of the first dee and the second dee has a bias voltage applied thereto; and an extraction channel to receive a beam of particles from the cavity for output from the particle accelerator. This example synchrocyclotron may include one or more of the following features, either alone or in combination.


The first dee may have a first bias voltage applied thereto and the second dee may have a second bias voltage applied thereto, where the first bias voltage is different from the second bias voltage. The first dee may have the bias voltage applied thereto and the second dee may be electrically grounded.


In an example, a proton therapy system includes the foregoing synchrocyclotron, and a gantry on which the synchrocyclotron is mounted. The gantry is rotatable relative to a patient position. Protons are output essentially directly from the synchrocyclotron to the patient position.


In an example, a particle therapy system may include: a synchrocyclotron to output a particle beam comprised of pulses; and a scanning system for the synchrocyclotron to scan the particle beam across at least part of an irradiation target. The scanning system may be configured to scan the particle beam in two dimensions that are angled relative to (e.g., perpendicular to) a longitudinal direction of the particle beam. The particle beam makes a spot at the irradiation target. The synchrocyclotron is controllable to vary a width of the pulses so as to vary an intensity of the particle beam between different spots on the irradiation target during scanning. Implementations of the particle therapy system may include one or more of the following features, either alone or in combination.


The synchrocyclotron may include a particle source, and the particle source may be controllable to activate for periods of time to generate pulses of the particle beam that vary in width. The synchrocyclotron may be configured to sweep between low and high voltages, and a rate (or speed) of the voltage sweep may be controllable to vary a width of the pulses. The particle source may include first and second cathodes to generate a plasma stream from gas. The pulses of particle beam are extractable from the plasma stream. The gas may be a combination of hydrogen and less than 25% of a noble gas or a combination of hydrogen and less than 10% of a noble gas. The gas may be a combination of hydrogen and helium. The helium may be less than 25% of a composition of the gas. In another example, the helium may be than 10% of a composition of the gas.


The scanning system may include: a magnet to affect a direction of the particle beam to scan the particle beam in the two dimensions across at least part of the irradiation target; and a degrader to change an energy of the beam prior to output of the particle beam to the irradiation target. The degrader may be down-beam of the magnet relative to the synchrocyclotron.


The synchrocyclotron may include a voltage source to provide a radio frequency (RF) voltage to a cavity to accelerate particles from a plasma column, where the cavity has a magnetic field causing particles accelerated from the plasma column to move orbitally within the cavity; an extraction channel to receive the particles accelerated from the plasma column and to output the received particles from the cavity; and a regenerator to provide a magnetic field bump within the cavity to thereby change successive orbits of the particles accelerated from the plasma column so that, eventually, particles output to the extraction channel. The magnetic field may be between 4 Tesla (T) and 20 T (or between 6 T and 20 T) and the magnetic field bump may be at most 2 Tesla.


Two or more of the features described in this disclosure (e.g., two or more methods of controlling the intensity of a particle beam), including those described in this summary section, may be combined to form implementations not specifically described herein.


Control of the various systems described herein, or portions thereof, may be implemented via a computer program product that includes instructions that are stored on one or more non-transitory machine-readable storage media, and that are executable on one or more processing devices. The systems described herein, or portions thereof, may be implemented as an apparatus, method, or electronic system that may include one or more processing devices and memory to store executable instructions to implement control of the stated functions.


The details of one or more implementations are set forth in the accompanying drawings and the description below. Other features, objects, and advantages will be apparent from the description and drawings, and from the claims.





DESCRIPTION OF DRAWINGS


FIG. 1 is a perspective view of an example therapy system.



FIG. 2 is an exploded perspective view of components of an example synchrocyclotron.



FIGS. 3, 4, and 5 are cross-sectional views of an example synchrocyclotron.



FIG. 6 is a perspective view of an example synchrocyclotron.



FIG. 7 is a cross-sectional view of a portion of an example reverse bobbin and windings.



FIG. 8 is a cross sectional view of an example cable-in-channel composite conductor.



FIG. 9 is a cross-sectional view of an example particle source.



FIG. 10 is a perspective view of an example dee plate and an example dummy dee.



FIG. 11 is a perspective view of an example vault.



FIG. 12 is a perspective view of an example treatment room with a vault.



FIG. 13 shows a patient positioned relative to an example particle accelerator.



FIG. 14 shows a patient positioned within an example inner gantry in a treatment room.



FIGS. 15 and 16 show an example particle source.



FIG. 17 is a graph showing an example voltage sweep, extraction window, and particle source pulse width.



FIG. 18 is a perspective view of example active and dummy dees that may be used with the particle therapy system described herein.



FIG. 19 is a side view of an example scanning system.



FIG. 20 is a perspective view of the example scanning system.



FIGS. 21 and 22 are front and perspective views, respectively, of an example scanning magnet that may be used in the example scanning system.



FIG. 23 is a perspective view of an example range modulator that may be used in the example scanning system.



FIG. 24 is a perspective view of motion of a plate from the range modulator into/out of the beam path.





Like reference symbols in the various drawings indicate like elements.


DETAILED DESCRIPTION
Overview

Described herein is an example of a particle accelerator for use in an example system, such as a proton or ion therapy system. The system includes a particle accelerator—in this example, a synchrocyclotron—mounted on a gantry. The gantry enables the accelerator to be rotated around a patient position, as explained in more detail below. In some implementations, the gantry is steel and has two legs mounted for rotation on two respective bearings that lie on opposite sides of a patient. The particle accelerator is supported by a steel truss that is long enough to span a treatment area in which the patient lies and that is attached stably at both ends to the rotating legs of the gantry. As a result of rotation of the gantry around the patient, the particle accelerator also rotates.


In an example implementation, the particle accelerator (e.g., the synchrocyclotron) includes a cryostat that holds a superconducting coil for conducting a current that generates a magnetic field (B). In this example, the cryostat uses liquid helium (He) to maintain the coil at superconducting temperatures, e.g., 4° Kelvin (K). Magnetic yokes are adjacent (e.g., around) the cryostat, and define a cavity in which particles are accelerated. The cryostat is attached to the magnetic yokes through straps or the like.


In an example implementation, the particle accelerator includes a particle source (e.g., a Penning Ion Gauge—PIG source) to provide a plasma column to the cavity. Hydrogen gas is ionized to produce the plasma column. A voltage source provides a radio frequency (RF) voltage to the cavity to accelerate particles from the plasma column. As noted, in this example, the particle accelerator is a synchrocyclotron. Accordingly, the RF voltage is swept across a range of frequencies to account for relativistic effects on the particles (e.g., increasing particle mass) as their velocity increases during acceleration and the decreasing magnetic field produced to maintain axial focusing of the particles. The magnetic field produced by the coil causes particles accelerated from the plasma column to accelerate orbitally within the cavity. A magnetic field regenerator is positioned near the outer edge of the cavity and may be used to adjust the existing magnetic field at this location to thereby change locations of successive orbits of the particles accelerated from the plasma column so that, eventually, the particles output to an extraction channel that passes through the yokes. The extraction channel receives particles accelerated from the plasma column and outputs the received particles from the cavity. Elements both inside and outside the extraction channel shape and focus the particle beam.


A control system may be used to select the intensity of the particle beam. For example, one or more parameters or features of the particle accelerator may be controlled or otherwise adjusted to output the particle beam with the selected intensity. The selected intensity may be constant or variable. The example systems described herein use techniques to control the intensity of a particle beam, e.g., to vary the dose and dose rate of a particle beam delivered to a patient. A description of these techniques is provided below, followed by a description of an example particle therapy system in which those techniques may be implemented.


In an example technique, the intensity of the particle beam can be controlled by varying the time duration of the pulse of particle pulses extracted from the plasma column. In more detail, the RF voltage sweeps from a starting (e.g., maximum) frequency (e.g., 135 MHz) to an ending (e.g., minimum) frequency (e.g., 90 MHz). The particle source is activated for a period of time during the RF sweep to produce a plasma column. For example, in some implementations, the particle source is activated at 132 MHz for a period of time. During that time, particles are extracted from the plasma column by the electric field produced by the RF voltage. The extracted particles accelerate outwardly in orbits as the RF voltage frequency drops, keeping pace with the decreasing magnetic field and increasing relativistic mass until the particles are swept out a time (e.g., about 600 microseconds) later. Changing the duration for which the particle source is activated changes the width of the pulse of particles that is extracted from the plasma column during a frequency sweep. Increasing the pulse width causes an increase in the amount of particles extracted and thus an increase in the intensity of the particle beam. Decreasing the pulse width causes a decrease in the amount of particles extracted and thus a decrease in the intensity of the particle beam.


In another example technique, the intensity of the particle beam can be controlled by changing a voltage applied to cathodes in the particle source. In this regard, the plasma column is generated by applying a voltage to two cathodes of the particle source, and by outputting a gas, such as hydrogen (H2), in the vicinity of the cathodes. The voltage applied to the cathodes ionizes the hydrogen and the background magnetic field collimates the ionized hydrogen to thereby produce the plasma column. Increasing the cathode voltage causes an increase in the amount of ions in the plasma column, and decreasing the cathode voltage causes a decrease in the amount of ions in the plasma column. When more ions are present in the plasma column, more ions can be extracted during the RF voltage sweep, thereby increasing the intensity of the particle beam. When fewer ions are present in the plasma column, fewer ions can be extracted during the RF voltage sweep, thereby decreasing the intensity of the particle beam.


In another example technique, the intensity of the particle beam can be controlled by varying the amount of hydrogen supplied to the particle source. For example, increasing the amount of hydrogen supplied to the particle source results in more opportunity for ionization in the plasma column in response to the cathode voltage. Conversely, decreasing the amount of hydrogen supplied to the particle source results in less opportunity for ionization in the plasma column in response to the cathode voltage. As noted above, when more particles are present in the plasma column, more particles are extracted during the RF voltage sweep, thereby increasing the intensity of the particle beam. When fewer particles are present in the plasma column, fewer particles are extracted during the RF voltage sweep, thereby decreasing the intensity of the particle beam.


In another example technique, the intensity of the particle beam can be controlled by varying the magnitude of the RF voltage used to extract particles from the plasma column. For example, increasing the magnitude of the RF voltage causes more particles to be extracted from the plasma column. Conversely, decreasing the magnitude of the RF voltage causes fewer particles to be extracted from the plasma column. When more particles are extracted, the particle beam increases in intensity. Conversely, when fewer particles are extracted, the particle beam decreases in intensity.


In another example technique, the intensity of the particle beam can be controlled by varying the starting time during the frequency sweep at which the particle source is activated and, thus, during which particles are extracted. More specifically, there is a finite window during the frequency sweep during which particles can be extracted from the plasma column. In an example implementation, the frequency sweeps from about 135 MHz to about 90 MHz at a substantially constant rate. In this example, particles can be extracted at about the beginning of the downward slope between starting and ending frequencies, e.g., between 132 MHz and 131 MHz respectively, and the particle source can be activated for a period of time, e.g., for about 0.1 μs to 100 μs (or e.g., 1 μs to 10 μs up to about 40 μs). Changing the frequency at which the particle source is activated affects the amount of particles that are extracted from the particle beam and therefore the intensity of the particle beam.


In another example technique, pulse blanking may be used to control the intensity of the particle beam. In this regard, the frequency sweep is repeated a number of times per second (e.g., 500 times/second). The particle source could be activated for each frequency sweep (e.g., every 2 ms). Pulse blanking reduces the number of particles extracted from the particle beam by not activating the particle source during every frequency sweep. To achieve maximum beam intensity, the particle source may be activated every frequency sweep. To reduce beam intensity, the particle source may be activated less frequently, e.g., every second, third, hundredth, etc. sweep.


In another example technique, the intensity of the particle beam can be controlled by applying a DC bias voltage to one or more dees used to apply the RF voltage to the particle accelerator cavity. In this regard, the particle accelerator includes an active dee plate (or simply “dee”) that is a hollow metal structure having two semicircular surfaces that enclose a cavity in which the protons are accelerated during their rotation around the space enclosed by the magnet structure. The active dee is driven by a RF signal that is applied at the end of a radio-frequency transmission line to impart an electric field into the cavity. The RF field is made to vary in time as the accelerated particle beam increases in distance from the geometric center. A “dummy” dee comprises a rectangular metal wall with a slot for the beam that is spaced near to the exposed rim of the active dee. In some implementations, the dummy dee is grounded to the vacuum chamber and magnet yoke.


Applying RF voltage in the presence of a strong magnetic field can cause multi-pactoring, which can reduce the magnitude of the RF field and, in some cases, cause an electrical short. To reduce the amount of multi-pactoring, and thereby maintain the RF field, DC bias voltage may be applied to the active dee and, in some implementations, also to the dummy dee. In some implementations, the differential bias voltage between the active dee and dummy dee may be controlled to reduce multi-pactoring and thereby increase beam intensity. For example, in some implementations, there may be a 50% differential between the DC bias voltage on the active dee and dummy dee (e.g., a −1.9 KV DC bias voltage may be applied to the dummy dee and a −1.5 KV DC bias voltage may be applied to the active dee).


In another example technique, the intensity of the particle beam can be controlled by controlling the rate at which the RF voltage is swept (e.g., the slope of the decrease). By decreasing the slope, it is possible to increase the amount of time during which particles can be extracted from the plasma column. As a result, more particles can be extracted, thereby increasing the intensity of the particle beam. The converse is also true, e.g., by increasing the slope, the amount of time during which particles can be extracted from the plasma column can be decreased, which can result in a decrease in particle beam intensity.


The foregoing techniques for controlling the intensity of a particle beam in a particle accelerator may be used individually in a single particle accelerator, or any two or more of those techniques may be used in any appropriate combination in a single particle accelerator. The techniques are not limited to use with a particle therapy system, but rather may be used in any appropriate particle accelerator.


An example of a particle therapy system in which the foregoing techniques may be used is provided below.


Example Particle Therapy System

Referring to FIG. 1, a charged particle radiation therapy system 500 includes a beam-producing particle accelerator 502 having a weight and size small enough to permit it to be mounted on a rotating gantry 504 with its output directed straight (that is, essentially directly) from the accelerator housing toward a patient 506.


In some implementations, the steel gantry has two legs 508, 510 mounted for rotation on two respective bearings 512, 514 that lie on opposite sides of the patient. The accelerator is supported by a steel truss 516 that is long enough to span a treatment area 518 in which the patient lies (e.g., twice as long as a tall person, to permit the person to be rotated fully within the space with any desired target area of the patient remaining in the line of the beam) and is attached stably at both ends to the rotating legs of the gantry.


In some examples, the rotation of the gantry is limited to a range 520 of less than 360 degrees, e.g., about 180 degrees, to permit a floor 522 to extend from a wall of the vault 524 that houses the therapy system into the patient treatment area. The limited rotation range of the gantry also reduces the required thickness of some of the walls, which provide radiation shielding of people outside the treatment area. A range of 180 degrees of gantry rotation is enough to cover all treatment approach angles, but providing a larger range of travel can be useful. For example the range of rotation may be between 180 and 330 degrees and still provide clearance for the therapy floor space.


The horizontal rotational axis 532 of the gantry is located nominally one meter above the floor where the patient and therapist interact with the therapy system. This floor is positioned about 3 meters above the bottom floor of the therapy system shielded vault. The accelerator can swing under the raised floor for delivery of treatment beams from below the rotational axis. The patient couch moves and rotates in a substantially horizontal plane parallel to the rotational axis of the gantry. The couch can rotate through a range 534 of about 270 degrees in the horizontal plane with this configuration. This combination of gantry and patient rotational ranges and degrees of freedom allow the therapist to select virtually any approach angle for the beam. If needed, the patient can be placed on the couch in the opposite orientation and then all possible angles can be used.


In some implementations, the accelerator uses a synchrocyclotron configuration having a very high magnetic field superconducting electromagnetic structure. Because the bend radius of a charged particle of a given kinetic energy is reduced in direct proportion to an increase in the magnetic field applied to it, the very high magnetic field superconducting magnetic structure permits the accelerator to be made smaller and lighter. The synchrocyclotron uses a magnetic field that is uniform in rotation angle and falls off in strength with increasing radius. Such a field shape can be achieved regardless of the magnitude of the magnetic field, so in theory there is no upper limit to the magnetic field strength (and therefore the resulting particle energy at a fixed radius) that can be used in a synchrocyclotron.


Superconducting materials lose their superconducting properties in the presence of very high magnetic fields. High performance superconducting wire windings are used to allow very high magnetic fields to be achieved.


Superconducting materials typically need to be cooled to low temperatures for their superconducting properties to be realized. In some examples described here, cryo-coolers are used to bring the superconducting coil windings to temperatures near absolute zero. Using cryo-coolers can reduce complexity and cost.


The synchrocyclotron is supported on the gantry so that the beam is generated directly in line with the patient. The gantry permits rotation of the cyclotron about a horizontal rotational axis that contains a point (isocenter 540) within, or near, the patient. The split truss that is parallel to the rotational axis, supports the cyclotron on both sides.


Because the rotational range of the gantry is limited, a patient support area can be accommodated in a wide area around the isocenter. Because the floor can be extended broadly around the isocenter, a patient support table can be positioned to move relative to and to rotate about a vertical axis 542 through the isocenter so that, by a combination of gantry rotation and table motion and rotation, any angle of beam direction into any part of the patient can be achieved. The two gantry arms are separated by more than twice the height of a tall patient, allowing the couch with patient to rotate and translate in a horizontal plane above the raised floor.


Limiting the gantry rotation angle allows for a reduction in the thickness of at least one of the walls surrounding the treatment room. Thick walls, typically constructed of concrete, provide radiation protection to individuals outside the treatment room. A wall downstream of a stopping proton beam may be about twice as thick as a wall at the opposite end of the room to provide an equivalent level of protection. Limiting the range of gantry rotation enables the treatment room to be sited below earth grade on three sides, while allowing an occupied area adjacent to the thinnest wall reducing the cost of constructing the treatment room.


In the example implementation shown in FIG. 1, the superconducting synchrocyclotron 502 operates with a peak magnetic field in a pole gap of the synchrocyclotron of 8.8 Tesla. The synchrocyclotron produces a beam of protons having an energy of 250 MeV. In other implementations the field strength could be in the range of 6 to 20 Tesla or 4 to 20 Tesla and the proton energy could be in the range of 150 to 300 MeV


The radiation therapy system described in this example is used for proton radiation therapy, but the same principles and details can be applied in analogous systems for use in heavy ion (ion) treatment systems.


As shown in FIGS. 2, 3, 4, 5, and 6, an example synchrocyclotron 10 (e.g., 502 in FIG. 1) includes a magnet system 12 that contains an particle source 90, a radiofrequency drive system 91, and a beam extraction system 38. The magnetic field established by the magnet system has a shape appropriate to maintain focus of a contained proton beam using a combination of a split pair of annular superconducting coils 40, 42 and a pair of shaped ferromagnetic (e.g., low carbon steel) pole faces 44, 46.


The two superconducting magnet coils are centered on a common axis 47 and are spaced apart along the axis. As shown in FIGS. 7 and 8, the coils are formed by of Nb3Sn-based superconducting 0.8 mm diameter strands 48 (that initially comprise a niobium-tin core surrounded by a copper sheath) deployed in a twisted cable-in-channel conductor geometry. After seven individual strands are cabled together, they are heated to cause a reaction that forms the final (brittle) superconducting material of the wire. After the material has been reacted, the wires are soldered into the copper channel (outer dimensions 3.18×2.54 mm and inner dimensions 2.08×2.08 mm) and covered with insulation 52 (in this example, a woven fiberglass material). The copper channel containing the wires 53 is then wound in a coil having a rectangular cross-section of 8.55 cm×19.02 cm, having 26 layers and 49 turns per layer. The wound coil is then vacuum impregnated with an epoxy compound. The finished coils are mounted on an annular stainless steel reverse bobbin 56. Heater blankets 55 are placed at intervals in the layers of the windings to protect the assembly in the event of a magnet quench.


The entire coil can then be covered with copper sheets to provide thermal conductivity and mechanical stability and then contained in an additional layer of epoxy. The precompression of the coil can be provided by heating the stainless steel reverse bobbin and fitting the coils within the reverse bobbin. The reverse bobbin inner diameter is chosen so that when the entire mass is cooled to 4 K, the reverse bobbin stays in contact with the coil and provides some compression. Heating the stainless steel reverse bobbin to approximately 50 degrees C. and fitting coils at a temperature of 100 degrees Kelvin can achieve this.


The geometry of the coil is maintained by mounting the coils in a reverse rectangular bobbin 56 to exert a restorative force 60 that works against the distorting force produced when the coils are energized. As shown in FIG. 5, the coil position is maintained relative to the magnet yoke and cryostat using a set of warm-to-cold support straps 402, 404, 406. Supporting the cold mass with thin straps reduces the heat leakage imparted to the cold mass by the rigid support system. The straps are arranged to withstand the varying gravitational force on the coil as the magnet rotates on board the gantry. They withstand the combined effects of gravity and the large de-centering force realized by the coil when it is perturbed from a perfectly symmetric position relative to the magnet yoke. Additionally the links act to reduce dynamic forces imparted on the coil as the gantry accelerates and decelerates when its position is changed. Each warm-to-cold support includes one S2 fiberglass link and one carbon fiber link. The carbon fiber link is supported across pins between the warm yoke and an intermediate temperature (50-70 K), and the S2 fiberglass link 408 is supported across the intermediate temperature pin and a pin attached to the cold mass. Each link is 5 cm long (pin center to pin center) and is 17 mm wide. The link thickness is 9 mm. Each pin is made of high strength stainless steel and is 40 mm in diameter.


Referring to FIG. 3, the field strength profile as a function of radius is determined largely by choice of coil geometry and pole face shape; the pole faces 44, 46 of the permeable yoke material can be contoured to fine tune the shape of the magnetic field to ensure that the particle beam remains focused during acceleration.


The superconducting coils are maintained at temperatures near absolute zero (e.g., about 4 degrees Kelvin) by enclosing the coil assembly (the coils and the bobbin) inside an evacuated annular aluminum or stainless steel cryostatic chamber 70 that provides a free space around the coil structure, except at a limited set of support points 71, 73. In an alternate version (FIG. 4) the outer wall of the cryostat may be made of low carbon steel to provide an additional return flux path for the magnetic field.


In some implementations, the temperature near absolute zero is achieved and maintained using one single-stage Gifford-McMahon cryo-cooler and three two-stage Gifford McMahon cryo-coolers. Each two stage cryo-cooler has a second stage cold end attached to a condenser that recondenses Helium vapor into liquid Helium. The cryo-cooler heads are supplied with compressed Helium from a compressor. The single-stage Gifford-McMahon cryo-cooler is arranged to cool high temperature (e.g., 50-70 degrees Kelvin) leads that supply current to the superconducting windings.


In some implementations, the temperature near absolute zero is achieved and maintained using two Gifford-McMahon cryo-coolers 72, 74 that are arranged at different positions on the coil assembly. Each cryo-cooler has a cold end 76 in contact with the coil assembly. The cryo-cooler heads 78 are supplied with compressed Helium from a compressor 80. Two other Gifford-McMahon cryo-coolers 77, 79 are arranged to cool high temperature (e.g., 60-80 degrees Kelvin) leads that supply current to the superconducting windings.


The coil assembly and cryostatic chambers are mounted within and fully enclosed by two halves 81, 83 of a pillbox-shaped magnet yoke 82. In this example, the inner diameter of the coil assembly is about 74.6 cm. The iron yoke 82 provides a path for the return magnetic field flux 84 and magnetically shields the volume 86 between the pole faces 44, 46 to prevent external magnetic influences from perturbing the shape of the magnetic field within that volume. The yoke also serves to decrease the stray magnetic field in the vicinity of the accelerator. In some implementations, the synchrocyclotron may have an active return system to reduce stray magnetic fields. An example of an active return system is described in U.S. patent application Ser. No. 13/907,601, which was filed on May 31, 2013, the contents of which are incorporated herein by reference. In the active return system, the relatively large magnetic yokes described herein are replaced by smaller magnetic structures, referred to as pole pieces. Superconducting coils run current opposite to the main coils described herein in order to provide magnetic return and thereby reduce stray magnetic fields


As shown in FIGS. 3 and 9, the synchrocyclotron includes a particle source 90 of a Penning ion gauge geometry located near the geometric center 92 of the magnet structure 82. The particle source may be as described below, or the particle source may be of the type described in U.S. patent application Ser. No. 11/948,662 incorporated herein by reference.


Particle source 90 is fed from a supply 99 of hydrogen through a gas line 101 and tube 194 that delivers gaseous hydrogen. Electric cables 94 carry an electric current from a current source 95 to stimulate electron discharge from cathodes 192, 190 that are aligned with the magnetic field, 200.


In this example, the discharged electrons ionize the gas exiting through a small hole from tube 194 to create a supply of positive ions (protons) for acceleration by one semicircular (dee-shaped) radio-frequency plate 100 that spans half of the space enclosed by the magnet structure and one dummy dee plate 102. In the case of an interrupted particle source (an example of which is described in U.S. patent application Ser. No. 11/948,662), all (or a substantial part) of the tube containing plasma is removed at the acceleration region, thereby allowing ions to be more rapidly accelerated in a relatively high magnetic field.


As shown in FIG. 10, the dee plate 100 is a hollow metal structure that has two semicircular surfaces 103, 105 that enclose a space 107 in which the protons are accelerated during half of their rotation around the space enclosed by the magnet structure. A duct 109 opening into the space 107 extends through the yoke to an external location from which a vacuum pump 111 can be attached to evacuate the space 107 and the rest of the space within a vacuum chamber 119 in which the acceleration takes place. The dummy dee 102 comprises a rectangular metal ring that is spaced near to the exposed rim of the dee plate. The dummy dee is grounded to the vacuum chamber and magnet yoke. The dee plate 100 is driven by a radio-frequency signal that is applied at the end of a radio-frequency transmission line to impart an electric field in the space 107. The radio frequency electric field is made to vary in time as the accelerated particle beam increases in distance from the geometric center. The radio frequency electric field may be controlled in the manner described in U.S. patent application Ser. No. 11/948,359, entitled “Matching A Resonant Frequency Of A Resonant Cavity To A Frequency Of An Input Voltage”, the contents of which are incorporated herein by reference.


For the beam emerging from the centrally located particle source to clear the particle source structure as it begins to spiral outward, a large voltage difference is required across the radio frequency plates. 20,000 Volts is applied across the radio frequency plates. In some versions from 8,000 to 20,000 Volts may be applied across the radio frequency plates. To reduce the power required to drive this large voltage, the magnet structure is arranged to reduce the capacitance between the radio frequency plates and ground. This is done by forming holes with sufficient clearance from the radio frequency structures through the outer yoke and the cryostat housing and making sufficient space between the magnet pole faces.


The high voltage alternating potential that drives the dee plate has a frequency that is swept downward during the accelerating cycle to account for the increasing relativistic mass of the protons and the decreasing magnetic field. The dummy dee does not require a hollow semi-cylindrical structure as it is at ground potential along with the vacuum chamber walls. Other plate arrangements could be used such as more than one pair of accelerating electrodes driven with different electrical phases or multiples of the fundamental frequency. The RF structure can be tuned to keep the Q high during the required frequency sweep by using, for example, a rotating capacitor having intermeshing rotating and stationary blades. During each meshing of the blades, the capacitance increases, thus lowering the resonant frequency of the RF structure. The blades can be shaped to create a precise frequency sweep required. A drive motor for the rotating condenser can be phase locked to the RF generator for precise control. One bunch of particles is accelerated during each meshing of the blades of the rotating condenser.


The vacuum chamber 119 in which the acceleration occurs is a generally cylindrical container that is thinner in the center and thicker at the rim. The vacuum chamber encloses the RF plates and the particle source and is evacuated by the vacuum pump 111. Maintaining a high vacuum insures that accelerating ions are not lost to collisions with gas molecules and enables the RF voltage to be kept at a higher level without arcing to ground.


Protons traverse a generally spiral orbital path beginning at the particle source. In half of each loop of the spiral path, the protons gain energy as they pass through the RF electric field in space 107. As the ions gain energy, the radius of the central orbit of each successive loop of their spiral path is larger than the prior loop until the loop radius reaches the maximum radius of the pole face. At that location a magnetic and electric field perturbation directs ions into an area where the magnetic field rapidly decreases, and the ions depart the area of the high magnetic field and are directed through an evacuated tube 38, referred to herein as the extraction channel, to exit the yoke of the cyclotron. A magnetic regenerator may be used to change the magnetic field perturbation to direct the ions. The ions exiting the cyclotron will tend to disperse as they enter the area of markedly decreased magnetic field that exists in the room around the cyclotron. Beam shaping elements 107, 109 in the extraction channel 38 redirect the ions so that they stay in a straight beam of limited spatial extent.


The magnetic field within the pole gap needs to have certain properties to maintain the beam within the evacuated chamber as it accelerates. The magnetic field index n, which is shown below,

n=−(r/B)dB/dr,

should be kept positive to maintain this “weak” focusing. Here r is the radius of the beam and B is the magnetic field. Additionally, in some implementations, the field index needs to be maintained below 0.2, because at this value the periodicity of radial oscillations and vertical oscillations of the beam coincide in a vr=2 vz resonance. The betatron frequencies are defined by vr=(1−n)1/2 and vz=n1/2. The ferromagnetic pole face is designed to shape the magnetic field generated by the coils so that the field index n is maintained positive and less than 0.2 in the smallest diameter consistent with a 250 MeV beam in the given magnetic field.


As the beam exits the extraction channel it is passed through a beam formation system 125 (FIG. 5) that can be programmably controlled to create a desired combination of scanning, scattering, and/or range modulation for the beam. Beam formation system 125 may be used in conjunction with an inner gantry 601 (FIG. 14) to direct a beam to the patient.


During operation, the plates absorb energy from the applied radio frequency field as a result of conductive resistance along the surfaces of the plates. This energy appears as heat and is removed from the plates using water cooling lines 108 that release the heat in a heat exchanger 113 (FIG. 3).


Stray magnetic fields exiting from the cyclotron are limited by both the pillbox magnet yoke (which also serves as a shield) and a separate magnetic shield 114. The separate magnetic shield includes of a layer 117 of ferromagnetic material (e.g., steel or iron) that encloses the pillbox yoke, separated by a space 116. This configuration that includes a sandwich of a yoke, a space, and a shield achieves adequate shielding for a given leakage magnetic field at lower weight.


As mentioned, the gantry allows the synchrocyclotron to be rotated about the horizontal rotational axis 532. The truss structure 516 has two generally parallel spans 580, 582. The synchrocyclotron is cradled between the spans about midway between the legs. The gantry is balanced for rotation about the bearings using counterweights 122, 124 mounted on ends of the legs opposite the truss.


The gantry is driven to rotate by an electric motor mounted to one or both of the gantry legs and connected to the bearing housings by drive gears. The rotational position of the gantry is derived from signals provided by shaft angle encoders incorporated into the gantry drive motors and the drive gears.


At the location at which the ion beam exits the cyclotron, the beam formation system 125 acts on the ion beam to give it properties suitable for patient treatment. For example, the beam may be spread and its depth of penetration varied to provide uniform radiation across a given target volume. The beam formation system can include passive scattering elements as well as active scanning elements.


All of the active systems of the synchrocyclotron (the current driven superconducting coils, the RF-driven plates, the vacuum pumps for the vacuum acceleration chamber and for the superconducting coil cooling chamber, the current driven particle source, the hydrogen gas source, and the RF plate coolers, for example), may be controlled by appropriate synchrocyclotron control electronics (not shown), which may include, e.g., one or more computers programmed with appropriate programs to effect control.


The control of the gantry, the patient support, the active beam shaping elements, and the synchrocyclotron to perform a therapy session is achieved by appropriate therapy control electronics (not shown).


As shown in FIGS. 1, 11, and 12, the gantry bearings are supported by the walls of a cyclotron vault 524. The gantry enables the cyclotron to be swung through a range 520 of 180 degrees (or more) including positions above, to the side of, and below the patient. The vault is tall enough to clear the gantry at the top and bottom extremes of its motion. A maze 146 sided by walls 148, 150 provides an entry and exit route for therapists and patients. Because at least one wall 152 is not in line with the proton beam directly from the cyclotron, it can be made relatively thin and still perform its shielding function. The other three side walls 154, 156, 150/148 of the room, which may need to be more heavily shielded, can be buried within an earthen hill (not shown). The required thickness of walls 154, 156, and 158 can be reduced, because the earth can itself provide some of the needed shielding.


Referring to FIGS. 12 and 13, for safety and aesthetic reasons, a therapy room 160 may be constructed within the vault. The therapy room is cantilevered from walls 154, 156, 150 and the base 162 of the containing room into the space between the gantry legs in a manner that clears the swinging gantry and also maximizes the extent of the floor space 164 of the therapy room. Periodic servicing of the accelerator can be accomplished in the space below the raised floor. When the accelerator is rotated to the down position on the gantry, full access to the accelerator is possible in a space separate from the treatment area. Power supplies, cooling equipment, vacuum pumps and other support equipment can be located under the raised floor in this separate space. Within the treatment room, the patient support 170 can be mounted in a variety of ways that permit the support to be raised and lowered and the patient to be rotated and moved to a variety of positions and orientations.


In system 602 of FIG. 14, a beam-producing particle accelerator of the type described herein, in this case synchrocyclotron 604, is mounted on rotating gantry 605. Rotating gantry 605 is of the type described herein, and can angularly rotate around patient support 606. This feature enables synchrocyclotron 604 to provide a particle beam directly to the patient from various angles. For example, as in FIG. 14, if synchrocyclotron 604 is above patient support 606, the particle beam may be directed downwards toward the patient. Alternatively, if synchrocyclotron 604 is below patient support 606, the particle beam may be directed upwards toward the patient. The particle beam is applied directly to the patient in the sense that an intermediary beam routing mechanism is not required. A routing mechanism, in this context, is different from a shaping or sizing mechanism in that a shaping or sizing mechanism does not re-route the beam, but rather sizes and/or shapes the beam while maintaining the same general trajectory of the beam.


Further details regarding an example implementation of the foregoing system may be found in U.S. Pat. No. 7,728,311, filed on Nov. 16, 2006 and entitled “Charged Particle Radiation Therapy”, and in U.S. patent application Ser. No. 12/275,103, filed on Nov. 20, 2008 and entitled “Inner Gantry”. The contents of U.S. Pat. No. 7,728,311 and in U.S. patent application Ser. No. 12/275,103 are hereby incorporated by reference into this disclosure.


In some implementations, the synchrocyclotron may be a variable-energy device, such as that described in U.S. patent application Ser. No. 13/916,401, filed on Jun. 12, 2013, the contents of which are incorporated by reference into this disclosure.


Example Implementations

Referring to FIG. 3, particle source 90 is deployed near to the magnetic center of synchrocyclotron 10 so that particles are present at the synchrocyclotron mid-plane, where they can be acted upon by the RF voltage field. As noted above, the particle source may have a Penning ion gauge (PIG) geometry. In the PIG geometry, two high voltage cathodes are placed about opposite each other so that they are aligned linearly. For example, one cathode may be on one side of the acceleration region and one cathode may be on the other side of the acceleration region and in line with the magnetic field lines. A gas tube 101 extends toward the acceleration region proximate to the particle source. When a relatively small amount of a gas (e.g., hydrogen/H2) occupies a region in the tube between the cathodes, a plasma column may be formed from the gas by applying a voltage to the cathodes. The applied voltage causes electrons to stream along the magnetic field lines, essentially parallel to the tube walls, and to ionize gas molecules that are concentrated inside the tube. The background magnetic field prevents scattering of the ionized gas particles and creates a plasma column between the cathodes.


In some implementations, the gas in gas tube 101 may include a mixture of hydrogen and one or more other gases. For example, the mixture may contain hydrogen and one or more of the noble gases, e.g., helium, neon, argon, krypton, xenon and/or radon (although the mixture is not limited to use with the noble gases). In some implementations, the mixture may be a mixture of hydrogen and helium. For example, the mixture may contain about 75% or more of hydrogen and about 25% or less of helium (with possible trace gases included). In another example, the mixture may contain about 90% or more of hydrogen and about 10% or less of helium (with possible trace gases included). In examples, the hydrogen/helium mixture may be any of the following: >95%/<5%, >90%/<10%, >85%/<15%, >80%/<20%, >75%/<20%, and so forth.


Possible advantages of using a noble (or other) gas in combination with hydrogen in the particle source may include: increased beam intensity, increased cathode longevity, and increased consistency of beam output.


An example of a PIG geometry particle source 700 that may be used in synchrocyclotron 10 is shown in FIGS. 15 and 16. Referring to FIG. 15, particle source 700 includes an emitter side 701 containing a gas feed 702 for receiving gas (e.g., hydrogen (H2), and a reflector side 704. A housing, or tube, 706 holds the gas. FIG. 16 shows particle source 700 passing through dummy dee 710 and adjacent to active (RF) dee 711. In operation, the magnetic field between active dee 711 and dummy dee 710 causes particles (e.g., protons) to accelerate outwardly. The acceleration is spiral to create orbits about the plasma column, with the particle-to-plasma-column radius progressively increasing. The radii of curvature of the spirals depend on a particle's mass, energy imparted to the particle by the RF field, and a strength of the magnetic field.


When the magnetic field is high, it can become difficult to impart enough energy to a particle so that it has a large enough radius of curvature to clear the physical housing of the particle source on its initial turn(s) during acceleration. The magnetic field is relatively high in the region of the particle source, e.g., on the order of 2 Tesla (T) or more (e.g., 4 T, 5 T, 6 T, 8 T, 8.8 T, 8.9 T, 9 T, 10.5 T, or more). As a result of this relatively high magnetic field, the initial particle-to-ion-source radius is relatively small for low energy particles, where low energy particles include particles that are first drawn from the plasma column. For example, such a radius may be on the order of 1 mm. Because the radii are so small, at least initially, some particles may come into contact with the particle source's housing area, thereby preventing further outward acceleration of such particles. Accordingly, the housing of particle source 700 is interrupted, or separated to form two parts, as shown in FIG. 16. That is, a portion of the particle source's housing may be entirely removed at the acceleration region 714, e.g., at about the point where the particles are to be drawn from the particle source. This interruption is labeled 715 in FIG. 16. The housing may also be removed for distances above, and below, the acceleration region. In an alternative implementation, a substantial portion (e.g., 30%, 40%, 50% or more), but not all, of the PIG source housing is removed, leaving the plasma beam partly exposed. Thus, portions of the PIG housing are separated from their counterpart portions, but there is not complete separation as was the case above.


In the synchrocyclotron described herein, a particle beam is extracted using a resonant extraction system. That is, radial oscillation of the beam is created by a magnetic perturbation inside the accelerator, which establishes a resonance of these oscillations. When a resonant extraction system is used, extraction efficiency is improved by limiting the phase space extent of the internal beam. With attention to the design of the magnetic and RF field generating structures, the phase space extent of the beam at extraction is determined by the phase space extent at the beginning of acceleration (e.g., at emergence from the particle source). As a result, relatively little beam may be lost at the entrance to the extraction channel and background radiation from the accelerator can be reduced.


Cathodes 717 may be “cold” cathodes. A cold cathode may be a cathode that is not heated by an external heat source. Also, the cathodes may be pulsed, meaning that they output plasma burst(s) periodically rather than continuously. When the cathodes are cold, and are pulsed, the cathodes are less subject to wear and can therefore last relatively long. Furthermore, pulsing the cathodes can eliminate the need to water-cool the cathodes. In one implementation, cathodes 717 pulse at a relatively high voltage, e.g., about 1 kV to about 4 kV, and moderate peak cathode discharge currents of about 50 mA to about 200 mA at a duty cycle between about 0.1% and about 1% or 2% at repetition rates between about 200 Hz to about 1 KHz. However, the particle source is not limited to these values.


Various aspects of example particle therapy system described herein may be computer-controlled. Computer controls may be effected through one or more signals output from the computer to various electronics on the particle therapy system. For example, the intensity of the particle beam generated by the particle therapy system may be measured, and the particle therapy system may be adjusted to control the intensity of the particle beam. The measurement and adjustment may occur once, at each use of the particle therapy system, in real-time (e.g., during treatment), or at other frequencies. In some implementations, the various parameters or other features of the particle accelerator described below may be varied, and the intensity of the resulting particle beam measured in order to determine if the appropriate result was achieved. If the appropriate result was not achieved, then the parameters or other features may be varied again and the results measured until the appropriate results are achieved.


In an example implementation, the time-width of pulses output by the particle source may be varied to control the intensity of the particle beam. In other words, the amount of time that the particle source is intermittently (e.g., periodically) activated is varied, thereby providing the plasma column for different periods of time and enabling extraction of different numbers of particles. For example, if the pulse width is increased, the number of particles extracted increases and, if the pulse width decreases, the number of particles extracted decreases. In some implementations, there is a linear relationship between the time that the particle source is on and the intensity of the particle beam. For example, the relationship may be one-to-one plus an offset. In an example implementation, the particle source may be pulsed within a frequency window that occurs during a frequency sweep between a maximum frequency of about 135 MHz and a minimum frequency of about 95 MHz or 90 MHz. For example, the particle source may be pulsed between 132 MHz and 131 MHz for a period of time. In an implementation, this period of time is about 40 μs; however, these values may vary or be different in other implementations. Failing to pulse the particle source outside of the frequency window can inhibit extraction of particles from the plasma column.



FIG. 17 is a graph showing the voltage sweep in the resonant cavity over time from a maximum frequency (e.g., 135 MHz) to a minimum frequency (e.g., 90 MHz or 95 MHz). The extraction window 720 occurs, in this example, between 132 MHz and 131 MHz. The width of pulse 721 may be varied to control the intensity of the particle beam output by the particle accelerator.


In other implementations, the voltage of cathodes 717 may be adjusted in order to control the amount of ionization in the plasma column, and thereby control the intensity of the particle beam output from the accelerator. Varying the voltage of cold cathodes can produce particularly sharp pulse edges.


In other implementations, the gas flow in tube 101 may be adjusted to increase or decrease the amount of hydrogen in the plasma column. As explained above, this increase or decrease in hydrogen can cause an increase or decrease in the amount of particles in the plasma column that are available for extraction. Thus, by varying the amount/flow of hydrogen provided by the particle source, it is possible to control the amount of particles available for extraction and thus the intensity of the resulting particle beam. For example, as explained above, when more particles are present in the plasma column, more particles are extracted during the RF voltage sweep, thereby increasing the intensity of the particle beam. When fewer particles are present in the plasma column, fewer particles are extracted during the RF voltage sweep, thereby decreasing the intensity of the particle beam.


In other implementations, increasing the magnitude of the RF voltage during the extraction period can increase the amount of particles extracted and thereby increase the intensity of the particle beam. In this regard, the magnitude of the RF voltage may be varied during the entire period of the RF sweep or it may be varied only during times that particles are extractable from the plasma column. For example, in some implementations, particles are extracted from the plasma column during the sweep period from 132 MHz to 131 MHz. The magnitude of the RF voltage may be increased during that period only or, in some cases, during periods that precede and follow the extraction period. In some example implementations, the time period during which the magnitude may be increased is 20-40 μs. Notably, these values are specific to one example particle accelerator, and the values, including frequency window and time period, may be different for different systems.


In other implementations, particle source 700 is controllable to provide pulses of the ionized plasma at specific frequencies proximate to a decrease from the maximum RF frequency to the minimum RF frequency during the voltage sweep. For example, referring to FIG. 17, pulse width 721 may be controlled to occur at any point between a starting (e.g., maximum) frequency 722 and an ending (e.g., minimum) frequency 723. The amount of particles extracted at various frequencies may be measured in order to determine the best location.


In some implementations, pulse widths may be varied by controlling the rate of the RF sweep. For example, slower RF sweeps may result on longer pulses and, thus, more particles (intensity) per pulse.


In other implementations, the voltage source is configurable to vary the RF voltage in order to control an intensity of the beam of particles. For example, the RF voltage may be swept over a time-scale from a high value to a low value. Initially, the RF voltage may be at a high value (e.g., constant for a period of time). There, the voltage is applied for an initial period of time (e.g., 20-40 μs). Then, the voltage is reduced, e.g., every 20 μs during the sweep so that its amplitude is adjusted to control the intensity of the particle beam. The slope of the decreasing magnetic field (versus time) may be increased or decreased in order to change the amount of particle extracted. In some implementations, the voltage may be applied in steps to control the particle beam output.


In other implementations, pulse-blanking may be used to control the intensity of the particle beam. For example, particle source 700 may be controlled to selectively output pulses of the ionized plasma. For example, the pulses may be output for a period during every voltage sweep; however, pulse output may be skipped in every Nth (N>1) sweep. So, for example, the control system may detect that there is 1% too much beam, in which case every 100th pulse may be skipped. In other implementations, pulses may be skipped more frequently, e.g., every second, third, tenth or any other appropriate numbered pulse may be skipped.


In other implementations, a bias voltage may be applied to the active dee and/or to the dummy dee to reduce the effects of multi-pactoring and thereby increase the intensity of the particle beam. In this regard, multi-pactoring occurs when electrons bounce between dee plates, causing additional electrons to be cast-off of the dee plates upon impact. The result can adversely affect the operation of the dee plates to the point of electrically shorting the dee plates.


To reduce the effects of multi-pactoring, a DC bias voltage may be applied to the active dee and/or to the dummy dee. This causes the background RF voltage to oscillate further away from ground than would otherwise be the case, thereby reducing electron transfer between dees. In an implementation, a DC bias voltage is applied to the dummy dee only, and the dummy dee is isolated from ground. In other implementations, differential DC bias voltages are applied to the dummy dee and the active dee. For example, a larger DC bias voltage may be applied to the dummy dee and a smaller DC bias voltage may be applied to the active dee. In some implementations, DC the bias plates 800, 801 of FIG. 18 may be added to the dummy dee 102. In this figure, the active dee is labeled 100.


In some implementations, the DC bias voltage differential (that is, the difference between the bias voltages applied to the active and dummy dees) may be within the +/−50% range. The specific amounts of the DC bias voltage may vary based on the level of the RF voltage. For example, 2.1 KV DC voltage may be applied to the dummy dee and 1.7 KV DC voltage may be applied to the active dee. In another example, 1.5 KV DC voltage may be applied to the dummy dee and 1.0 KV DC voltage may be applied to the active dee. In another example, 1.9 KV DC voltage may be applied to the dummy dee and 1.5 KV DC voltage may be applied to the active dee. In other implementations, different DC bias voltage may be used.


Referring to FIG. 19, at the output of extraction channel 802 of a particle accelerator (which may have the configuration shown in FIGS. 1 and 2) is a beam formation system, such as beam formation system 125. The beam formation system may be a scanning system. An example scanning system 806 is shown in FIG. 19, which may be used to scan the particle beam across at least part of an irradiation target. FIG. 20 also shows examples of the components of the scanning system include a scanning magnet 808, an ion chamber 809, and an energy degrader 810. Other components of the scanning system are not shown in FIG. 20.


In an example operation, scanning magnet 808 is controllable in two dimensions (e.g., Cartesian XY dimensions) to direct the particle beam across a part (e.g., a cross-section) of an irradiation target. Ion chamber 809 detects the dosage of the beam and feeds-back that information to a control system. Energy degrader 810 is controllable to move material into, and out of, the path of the particle beam to change the energy of the particle beam and therefore the depth to which the particle beam will penetrate the irradiation target.



FIGS. 21 and 22 shows views of an example scanning magnet 808. Scanning magnet 808 includes two coils 811, which control particle beam movement in the X direction, and two coils 812, which control particle beam movement in the Y direction. Control is achieved, in some implementations, by varying current through one or both sets of coils to thereby vary the magnetic field(s) produced thereby. By varying the magnetic field(s) appropriately, the particle beam can be moved in the X and/or Y direction across the irradiation target. In some implementations, the scanning magnet is not movable physically relative to the particle accelerator. In other implementations, the scanning magnet may be movable relative to the accelerator (e.g., in addition to the movement provided by the gantry).


In this example, ion chamber 809 detects dosage applied by the particle beam by detecting the numbers of ion pairs created within a gas caused by incident radiation. The numbers of ion pairs correspond to the dosage provided by the particle beam. That information is fed-back to a computer system that controls operation of the particle therapy system. The computer system (not shown), which may include memory and one or more processing devices, determines if the dosage detected by ion chamber is the intended dose. If the dosage is not as intended, the computer system may control the accelerator to interrupt production and/or output of the particle beam, and/or control the scanning magnet to prevent output of the particle beam to the irradiation target.



FIG. 23 shows a range modulator 815, which is an example implementation of energy degrader 810. In some implementations, such as that shown in FIG. 23, range modulator includes a series of plates 816. The plates may be made of one or more energy absorbing materials.


One or more of the plates is movable into, or out of, the beam path to thereby affect the energy of the particle beam and, thus, the depth of penetration of the particle beam within the irradiation target. For example, the more plates that are moved into the path of the particle beam, the more energy that will be absorbed by the plates, and the less energy the particle beam will have. Conversely, the fewer plates that are moved into the path of the particle beam, the less energy that will be absorbed by the plates, and the more energy the particle beam will have. Higher energy particle beams penetrate deeper into the irradiation target than do lower energy particle beams. In this context, “higher” and “lower” are meant as relative terms, and do not have any specific numeric connotations.


Plates are moved physically into, and out of, the path of the particle beam. For example, as shown in FIG. 24, a plate 816a moves along the direction of arrow 817 between positions in the path of the particle beam and outside the path of the particle beam. The plates are computer-controlled. Generally, the number of plates that are moved into the path of the particle beam corresponds to the depth at which scanning of an irradiation target is to take place. For example, the irradiation target can be divided into cross-sections, each of which corresponds to an irradiation depth. One or more plates of the range modulator can be moved into, or out of, the beam path to the irradiation target in order to achieve the appropriate energy to irradiate each of these cross-sections of the irradiation target.


In some implementations, a treatment plan is established prior to treating the irradiation target using scanning. The treatment plan may specify how scanning is to be performed for a particular irradiation target. In some implementations, the treatment plan specifies the following information: a type of scanning (e.g., spot scanning or raster scanning); scan locations (e.g., locations of spots to be scanned); magnet current per scan location; dosage-per-spot; locations (e.g., depths) of irradiation target cross-sections; particle beam energy per cross-section; plates or other types of pieces to move into the beam path for each particle beam energy; and so forth. Generally, spot scanning involves applying irradiation at discrete spots on an irradiation target and raster scanning involves moving a radiation spot across the radiation target. The concept of spot size therefore applies for both raster and spot scanning.


In some implementations, the intensity of spots in the scanning system may vary from spot-to-spot. Any of the techniques described herein may be used to vary the intensity of the particle beam from spot-to-spot. For example, the intensity of the particle beam may be varied from individual spot to individual spot, or from one group of spots to another group of spots, and so forth.


The pulse-width modulation techniques (PWM) described herein to vary the pulse width of pulses of the particle beam (and thereby vary the number of particles per pulse, i.e., pulse intensity) may be particularly useful for varying the intensity from spot-to-spot in the scanning system. PWM techniques may be particularly useful in a scanning context because they enable variation in spot intensity rather quickly, e.g., in a sub-second time-frame, and have a relatively wide dynamic range (although non-PWM techniques are still usable).


Any two more of the foregoing implementations may be used in an appropriate combination to affect the energy of a particle beam in the extraction channel. Likewise, individual features of any two more of the foregoing implementations may be used in an appropriate combination for the same purpose.


Elements of different implementations described herein may be combined to form other implementations not specifically set forth above. Elements may be left out of the processes, systems, apparatus, etc., described herein without adversely affecting their operation. Various separate elements may be combined into one or more individual elements to perform the functions described herein.


The example implementations described herein are not limited to use with a particle therapy system or to use with the example particle therapy systems described herein. Rather, the example implementations can be used in any appropriate system that directs accelerated particles to an output.


Additional information concerning the design of an example implementation of a particle accelerator that may be used in a system as described herein can be found in U.S. Provisional Application No. 60/760,788, entitled “High-Field Superconducting Synchrocyclotron” and filed Jan. 20, 2006; U.S. patent application Ser. No. 11/463,402, entitled “Magnet Structure For Particle Acceleration” and filed Aug. 9, 2006; and U.S. Provisional Application No. 60/850,565, entitled “Cryogenic Vacuum Break Pneumatic Thermal Coupler” and filed Oct. 10, 2006, all of which are incorporated herein by reference.


The following applications, all of which are filed on the same date as the subject application (entitled “CONTROLLING INTENSITY OF A PARTICLE BEAM” (Application No. 61/707,466)), are incorporated by reference into the subject application: the U.S. Provisional Application entitled “ADJUSTING ENERGY OF A PARTICLE BEAM” (Application No. 61/707,515), the U.S. Provisional Application entitled “ADJUSTING COIL POSITION” (Application No. 61/707,548), the U.S. Provisional Application entitled “FOCUSING A PARTICLE BEAM USING MAGNETIC FIELD FLUTTER” (Application No. 61/707,572), the U.S. Provisional Application entitled “MAGNETIC FIELD REGENERATOR” (Application No. 61/707,590), the U.S. Provisional Application entitled “FOCUSING A PARTICLE BEAM” (Application No. 61/707,704), the U.S. Provisional Application entitled “CONTROLLING PARTICLE THERAPY (Application No. 61/707,624), and the U.S. Provisional Application entitled “CONTROL SYSTEM FOR A PARTICLE ACCELERATOR” (Application No. 61/707,645).


The following are also incorporated by reference into the subject application: U.S. Pat. No. 7,728,311 which issued on Jun. 1, 2010, U.S. patent application Ser. No. 11/948,359 which was filed on Nov. 30, 2007, U.S. patent application Ser. No. 12/275,103 which was filed on Nov. 20, 2008, U.S. patent application Ser. No. 11/948,662 which was filed on Nov. 30, 2007, U.S. Provisional Application No. 60/991,454 which was filed on Nov. 30, 2007, U.S. Pat. No. 8,003,964 which issued on Aug. 23, 2011, U.S. Pat. No. 7,208,748 which issued on Apr. 24, 2007, U.S. Pat. No. 7,402,963 which issued on Jul. 22, 2008, U.S. patent application Ser. No. 13/148,000 filed Feb. 9, 2010, U.S. patent application Ser. No. 11/937,573 filed on Nov. 9, 2007, U.S. patent application Ser. No. 11/187,633, titled “A Programmable Radio Frequency Waveform Generator for a Synchrocyclotron,” filed Jul. 21, 2005, U.S. Provisional Application No. 60/590,089, filed on Jul. 21, 2004, U.S. patent application Ser. No. 10/949,734, titled “A Programmable Particle Scatterer for Radiation Therapy Beam Formation”, filed Sep. 24, 2004, and U.S. Provisional Application No. 60/590,088, filed Jul. 21, 2005.


Any features of the subject application may be combined with one or more appropriate features of the following: the U.S. Provisional Application entitled “ADJUSTING ENERGY OF A PARTICLE BEAM” (Application No. 61/707,515), the U.S. Provisional Application entitled “ADJUSTING COIL POSITION” (Application No. 61/707,548), the U.S. Provisional Application entitled “FOCUSING A PARTICLE BEAM USING MAGNETIC FIELD FLUTTER” (Application No. 61/707,572), the U.S. Provisional Application entitled “MAGNETIC FIELD REGENERATOR” (Application No. 61/707,590), the U.S. Provisional Application entitled “FOCUSING A PARTICLE BEAM” (Application No. 61/707,704), the U.S. Provisional Application entitled “CONTROLLING PARTICLE THERAPY (Application No. 61/707,624), and the U.S. Provisional Application entitled “CONTROL SYSTEM FOR A PARTICLE ACCELERATOR” (Application No. 61/707,645), U.S. Pat. No. 7,728,311 which issued on Jun. 1, 2010, U.S. patent application Ser. No. 11/948,359 which was filed on Nov. 30, 2007, U.S. patent application Ser. No. 12/275,103 which was filed on Nov. 20, 2008, U.S. patent application Ser. No. 11/948,662 which was filed on Nov. 30, 2007, U.S. Provisional Application No. 60/991,454 which was filed on Nov. 30, 2007, U.S. Pat. No. 8,003,964 which issued on Aug. 23, 2011, U.S. Pat. No. 7,208,748 which issued on Apr. 24, 2007, U.S. Pat. No. 7,402,963 which issued on Jul. 22, 2008, U.S. patent application Ser. No. 13/148,000 filed Feb. 9, 2010, U.S. patent application Ser. No. 11/937,573 filed on Nov. 9, 2007, U.S. patent application Ser. No. 11/187,633, titled “A Programmable Radio Frequency Waveform Generator for a Synchrocyclotron,” filed Jul. 21, 2005, U.S. Provisional Application No. 60/590,089, filed on Jul. 21, 2004, U.S. patent application Ser. No. 10/949,734, titled “A Programmable Particle Scatterer for Radiation Therapy Beam Formation”, filed Sep. 24, 2004, and U.S. Provisional Application No. 60/590,088, filed Jul. 21, 2005.


Except for the provisional application from which this patent application claims priority and the documents incorporated by reference above, no other documents are incorporated by reference into this patent application.


Other implementations not specifically described herein are also within the scope of the following claims.

Claims
  • 1. A synchrocyclotron comprising: a particle source to provide pulses of ionized plasma to a cavity;a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the ionized plasma outwardly;an extraction channel to receive a beam of particles from the cavity for output from the synchrocyclotron; anda control system comprising one or more processing devices to control the particle source to provide pulse widths of the ionized plasma in order to output the beam of particles at an intensity selected from different intensities;wherein the particle source comprises cathodes to provide voltage to ionize hydrogen to produce the ionized plasma, the cathodes being unheated by an external source.
  • 2. The synchrocyclotron of claim 1, wherein the particle source is configured to activate for a period of time in response to a control signal from the control system, where the particle source generates a pulse of ionized plasma when activated.
  • 3. The synchrocyclotron of claim 1, wherein the particle source is configured to generate pulses of ionized plasma periodically.
  • 4. The synchrocyclotron of claim 3, wherein the particle beam is output for a duration of about 0.1 μs to 100 μs.
  • 5. The synchrocyclotron of claim 3, wherein the particle beam is output for a duration of about 0.1 μs to 100 μs about every 2 ms.
  • 6. A proton therapy system comprising: the synchrocyclotron of claim 1; anda gantry on which the synchrocyclotron is mounted, the gantry for rotating the synchrocyclotron around a patient position.
  • 7. The synchrocyclotron of claim 1, wherein the voltage source comprises a first dee and a second dee, and wherein at least one of the first dee or the second dee has a bias voltage applied thereto.
  • 8. The synchrocyclotron of claim 1, wherein the voltage source is configured to sweep the RF voltage between a maximum frequency and a minimum frequency, and the particle source is controllable to affect the intensity by providing pulses of the ionized plasma at specific frequencies during a decrease from the maximum frequency of the RF voltage to the minimum frequency of the RF voltage.
  • 9. A synchrocyclotron comprising: a particle source to provide pulses of ionized plasma to a cavity, the particle source comprising cathodes to provide voltage to ionize hydrogen to produce the ionized plasma;a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the ionized plasma outwardly;an extraction channel to receive a beam of particles from the cavity for output from the synchrocyclotron; anda control system comprising one or more processing devices to control a voltage provided by the cathodes in order to output the beam of particles at an intensity selected from among different intensities;wherein the cathodes are unheated by an external source.
  • 10. The synchrocyclotron of claim 9, wherein the voltage is controllable such that increasing the voltage increases an intensity of the beam of particles and such that decreasing the voltage decreases the intensity of the beam of particles.
  • 11. A proton therapy system comprising: the synchrocyclotron of claim 9; anda gantry on which the synchrocyclotron is mounted, the gantry for rotating the synchrocyclotron around a patient position.
  • 12. The synchrocyclotron of claim 9, wherein the voltage source comprises a first dee and a second dee, and wherein at least one of the first dee or the second dee has a bias voltage applied thereto.
  • 13. The synchrocyclotron of claim 9, wherein the voltage source is configured to sweep the RF voltage between a maximum frequency and a minimum frequency, and the particle source is controllable to affect the intensity by providing pulses of the ionized plasma at specific frequencies during a decrease from the maximum frequency of the RF voltage to the minimum frequency of the RF voltage.
  • 14. A synchrocyclotron comprising: a particle source to provide pulses of ionized plasma to a cavity, the particle source comprising cathodes to provide voltage to ionize hydrogen to produce the ionized plasma;a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the ionized plasma outwardly;an extraction channel to receive a beam of particles from the cavity for output from the synchrocyclotron; anda control system comprising one or more processing devices to control the particle source to adjust an amount of the hydrogen between the cathodes in order to output the beam of particles at an intensity selected from among different intensities;wherein the cathodes are unheated by an external source.
  • 15. The synchrocyclotron of claim 14, wherein the amount of hydrogen is adjustable such that increasing the amount of hydrogen increases an intensity of the beam of particles and such that decreasing the amount of hydrogen decreases the intensity of the beam of particles.
  • 16. A proton therapy system comprising: the synchrocyclotron of claim 14; anda gantry on which the synchrocyclotron is mounted, the gantry for rotating the synchrocyclotron around a patient position.
  • 17. The synchrocyclotron of claim 14, wherein the voltage source comprises a first dee and a second dee, and wherein at least one of the first dee or the second dee has a bias voltage applied thereto.
  • 18. The synchrocyclotron of claim 14, wherein the voltage source is configured to sweep the RF voltage between a maximum frequency and a minimum frequency, and the particle source is controllable to affect the intensity by providing pulses of the ionized plasma at specific frequencies during a decrease from the maximum frequency of the RF voltage to the minimum frequency of the RF voltage.
  • 19. A synchrocyclotron comprising: a particle source to provide pulses of ionized plasma to a cavity;a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the ionized plasma outwardly;an extraction channel to receive a beam of particles from the cavity for output from the synchrocyclotron; anda control system comprising one or more processing devices to control the voltage source to provide a magnitude of the RF voltage in order to output the beam of particles at an intensity selected from among different intensities;wherein the particle source comprises cathodes to provide voltage to ionize hydrogen to produce the ionized plasma, the cathodes being unheated by an external source.
  • 20. The synchrocyclotron of claim 19, wherein the magnitude of the RF voltage is adjustable such that increasing the magnitude increases an intensity of the beam of particles and such that decreasing the magnitude decreases the intensity of the beam of particles.
  • 21. A proton therapy system comprising: the synchrocyclotron of claim 19; anda gantry on which the synchrocyclotron is mounted, the gantry for rotating the synchrocyclotron around a patient position.
  • 22. The synchrocyclotron of claim 19, wherein the voltage source comprises a first dee and a second dee, and wherein at least one of the first dee or the second dee has a bias voltage applied thereto.
  • 23. The synchrocyclotron of claim 19, wherein the voltage source is configured to sweep the RF voltage between a maximum frequency and a minimum frequency, and the particle source is controllable to affect the intensity by providing pulses of the ionized plasma at specific frequencies during a decrease from the maximum frequency of the RF voltage to the minimum frequency of the RF voltage.
  • 24. A synchrocyclotron comprising: a particle source to provide pulses of ionized plasma to a cavity;a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the ionized plasma outwardly, the RF voltage sweeping between a maximum frequency and a minimum frequency;an extraction channel to receive a beam of particles from the cavity for output from the synchrocyclotron; anda control system comprising one or more processing devices to control the particle source to output the beam of particles at an intensity selected from among different intensities, the particle source being controllable by the control system to provide pulses of the ionized plasma at specific frequencies during a decrease from the maximum frequency of the RF voltage to the minimum frequency of the RF voltage;wherein the particle source comprises cathodes to provide voltage to ionize hydrogen to produce the ionized plasma, the cathodes being unheated by an external source.
  • 25. The synchrocyclotron of claim 24, wherein the particle source is controllable to provide pulses of the ionized plasma between 132 MHz of RF voltage and 131 MHz of RF voltage from a decrease from a maximum frequency of about 135 MHz of the RF voltage.
  • 26. A proton therapy system comprising: the synchrocyclotron of claim 24; anda gantry on which the synchrocyclotron is mounted, the gantry for rotating the synchrocyclotron around a patient position.
  • 27. The synchrocyclotron of claim 24, wherein the voltage source comprises a first dee and a second dee, and wherein at least one of the first dee or the second dee has a bias voltage applied thereto.
  • 28. A synchrocyclotron comprising: a particle source to provide pulses of ionized plasma to a cavity;a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the ionized plasma outwardly;an extraction channel to receive a beam of particles from the cavity for output from the synchrocyclotron; anda control system comprising one or more processing devices to control the particle source to selectively output pulses of the ionized plasma in order to output the beam of particles at an intensity selected from among different intensities;wherein the particle source comprises cathodes to provide voltage to ionize hydrogen to produce the ionized plasma, the cathodes being unheated by an external source.
  • 29. The synchrocyclotron of claim 28, wherein the voltage source is configured to sweep the RF voltage periodically from a maximum frequency to a minimum frequency; and wherein selectively outputting the pulses comprises outputting pulses in certain ones of the RF voltage sweeps and not in others of the RF voltage sweeps.
  • 30. The synchrocyclotron of claim 28, wherein the voltage source is configured to sweep the RF voltage periodically from a maximum frequency to a minimum frequency; and wherein selectively outputting the pulses comprises skipping pulse output in every Nth (N>1) sweep.
  • 31. The synchrocyclotron of claim 28, wherein the control system is configured to perform operations comprising: selecting the intensity of the beam of particles.
  • 32. A proton therapy system comprising: the synchrocyclotron of claim 28; anda gantry on which the synchrocyclotron is mounted, the gantry for rotating the synchrocyclotron around a patient position.
  • 33. The synchrocyclotron of claim 28, wherein the voltage source comprises a first dee and a second dee, and wherein at least one of the first dee or the second dee has a bias voltage applied thereto.
  • 34. The synchrocyclotron of claim 28, wherein the voltage source is configured to sweep the RF voltage between a maximum frequency and a minimum frequency, and the particle source is controllable to affect the intensity by providing pulses of the ionized plasma at specific frequencies during a decrease from the maximum frequency of the RF voltage to the minimum frequency of the RF voltage.
  • 35. A synchrocyclotron comprising: a particle source to provide pulses of ionized plasma to a cavity;a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the ionized plasma outwardly;an extraction channel to receive a beam of particles from the cavity for output from the synchrocyclotron; anda control system comprising one or more processing devices to control the voltage source to vary a rate of change of the RF voltage in order to output the beam of particles at an intensity selected from among different intensities;wherein the particle source comprises cathodes to provide voltage to ionize hydrogen to produce the ionized plasma, the cathodes being unheated by an external source.
  • 36. A proton therapy system comprising: the synchrocyclotron of claim 35; anda gantry on which the synchrocyclotron is mounted, the gantry for rotating the synchrocyclotron around a patient position.
  • 37. The synchrocyclotron of claim 35, wherein the voltage source comprises a first dee and a second dee, and wherein at least one of the first dee or the second dee has a bias voltage applied thereto.
  • 38. The synchrocyclotron of claim 35, wherein the voltage source is configured to sweep the RF voltage between a maximum frequency and a minimum frequency, and the particle source is controllable to affect the intensity by providing pulses of the ionized plasma at specific frequencies during a decrease from the maximum frequency of the RF voltage to the minimum frequency of the RF voltage.
  • 39. A synchrocyclotron comprising: a particle source to provide pulses of ionized plasma to a cavity;a voltage source to provide a radio frequency (RF) voltage to the cavity to accelerate particles from the ionized plasma outwardly, the voltage source comprising a first dee and a second dee, wherein at least one of the first dee or the second dee has a bias voltage applied thereto; andan extraction channel to receive a beam of particles from the cavity for output from the synchrocyclotron;wherein the particle source comprises cathodes to provide voltage to ionize hydrogen to produce the ionized plasma, the cathodes being unheated by an external source.
  • 40. The synchrocyclotron of claim 39, wherein the first dee has a first bias voltage applied thereto and the second dee has a second bias voltage applied thereto, the first bias voltage being different from the second bias voltage.
  • 41. The synchrocyclotron of claim 39, wherein the first dee has the bias voltage applied thereto and the second dee is electrically grounded.
  • 42. A proton therapy system comprising: the synchrocyclotron of claim 39; anda gantry on which the synchrocyclotron is mounted, the gantry for rotating the synchrocyclotron around a patient position.
  • 43. The synchrocyclotron of claim 39, wherein the voltage source is configured to sweep the RF voltage between a maximum frequency and a minimum frequency, and the particle source is controllable to affect the intensity by providing pulses of the ionized plasma at specific frequencies during a decrease from the maximum frequency of the RF voltage to the minimum frequency of the RF voltage.
  • 44. The synchrocyclotron of claim 39, wherein the first dee comprises a DC bias plate, and the bias voltage is a DC bias voltage.
CROSS-REFERENCE TO RELATED APPLICATION

Priority is hereby claimed to U.S. Provisional Application No. 61/707,466, which was filed on Sep. 28, 2012. The contents of U.S. Provisional Application No. 61/707,466 are hereby incorporated by reference into this disclosure.

US Referenced Citations (658)
Number Name Date Kind
2280606 Roberts Apr 1942 A
2492324 Salisbury Dec 1949 A
2615129 Mcmillan Oct 1952 A
2616042 Ray Oct 1952 A
2659000 Salisbury Nov 1953 A
2701304 Dickinson Feb 1955 A
2789222 Martin et al. Apr 1957 A
2958327 Geissmann Nov 1960 A
3175131 Burleigh et al. Mar 1965 A
3432721 Naydan et al. Mar 1969 A
3582650 Avery Jun 1971 A
3679899 Dimeff Jul 1972 A
3689847 Verster Sep 1972 A
3757118 Hodge et al. Sep 1973 A
3868522 Bigham et al. Feb 1975 A
3886367 Castle, Jr. May 1975 A
3925676 Bigham et al. Dec 1975 A
3955089 McIntyre et al. May 1976 A
3958327 Marancik et al. May 1976 A
3992625 Schmidt et al. Nov 1976 A
4038622 Purcell Jul 1977 A
4047068 Ress et al. Sep 1977 A
4112306 Nunan Sep 1978 A
4129784 Tschunt et al. Dec 1978 A
4139777 Rautenbach Feb 1979 A
4197510 Szu Apr 1980 A
4220866 Taumann et al. Sep 1980 A
4230129 LeVeen Oct 1980 A
4256966 Heinz Mar 1981 A
4293772 Stieber Oct 1981 A
4336505 Meyer Jun 1982 A
4342060 Gibson Jul 1982 A
4345210 Tran Aug 1982 A
4353033 Karasawa Oct 1982 A
4425506 Brown et al. Jan 1984 A
4490616 Cipollina et al. Dec 1984 A
4507614 Prono et al. Mar 1985 A
4507616 Blosser et al. Mar 1985 A
4589126 Augustsson et al. May 1986 A
4598208 Brunelli et al. Jul 1986 A
4628523 Heflin Dec 1986 A
4633125 Blosser et al. Dec 1986 A
4641057 Blosser et al. Feb 1987 A
4641104 Blosser et al. Feb 1987 A
4651007 Perusek et al. Mar 1987 A
4680565 Jahnke Jul 1987 A
4705955 Mileikowsky Nov 1987 A
4710722 Jahnke Dec 1987 A
4726046 Nunan Feb 1988 A
4734653 Jahnke Mar 1988 A
4736173 Basil, Jr. et al. Apr 1988 A
4737727 Yamada et al. Apr 1988 A
4739173 Blosser et al. Apr 1988 A
4745367 Dustmann et al. May 1988 A
4754147 Maughan et al. Jun 1988 A
4763483 Olsen Aug 1988 A
4767930 Stieber et al. Aug 1988 A
4769623 Marsing et al. Sep 1988 A
4771208 Jongen et al. Sep 1988 A
4783634 Yamamoto et al. Nov 1988 A
4808941 Marsing Feb 1989 A
4812658 Koehler Mar 1989 A
4843333 Marsing et al. Jun 1989 A
4845371 Stieber Jul 1989 A
4865284 Gosis et al. Sep 1989 A
4868843 Nunan Sep 1989 A
4868844 Nunan Sep 1989 A
4870287 Cole et al. Sep 1989 A
4880985 Jones Nov 1989 A
4894541 Ono Jan 1990 A
4896206 Denham Jan 1990 A
4902993 Krevet Feb 1990 A
4904949 Wilson Feb 1990 A
4905267 Miller et al. Feb 1990 A
4917344 Prechter et al. Apr 1990 A
4943781 Wilson et al. Jul 1990 A
4945478 Merickel et al. Jul 1990 A
4968915 Wilson et al. Nov 1990 A
4987309 Klasen et al. Jan 1991 A
4992744 Fujita et al. Feb 1991 A
4996496 Kitamura et al. Feb 1991 A
5006759 Krispel Apr 1991 A
5010562 Hernandez et al. Apr 1991 A
5012111 Ueda Apr 1991 A
5017789 Young et al. May 1991 A
5017882 Finlan May 1991 A
5036290 Sonobe et al. Jul 1991 A
5039057 Prechter et al. Aug 1991 A
5039867 Nishihara et al. Aug 1991 A
5046078 Hernandez et al. Sep 1991 A
5072123 Johnsen Dec 1991 A
5111042 Sullivan et al. May 1992 A
5111173 Matsuda et al. May 1992 A
5117194 Nakanishi et al. May 1992 A
5117212 Yamamoto et al. May 1992 A
5117829 Miller et al. Jun 1992 A
5148032 Hernandez Sep 1992 A
5166531 Huntzinger Nov 1992 A
5189687 Bova et al. Feb 1993 A
5191706 Cosden Mar 1993 A
5240218 Dye Aug 1993 A
5260579 Yasuda et al. Nov 1993 A
5260581 Lesyna et al. Nov 1993 A
5278533 Kawaguchi Jan 1994 A
5285166 Hiramoto et al. Feb 1994 A
5297037 Ifuku Mar 1994 A
5317164 Kurokawa May 1994 A
5336891 Crewe Aug 1994 A
5341104 Anton et al. Aug 1994 A
5349198 Takanaka Sep 1994 A
5365742 Boffito et al. Nov 1994 A
5374913 Pissantezky et al. Dec 1994 A
5382914 Hamm et al. Jan 1995 A
5401973 McKeown et al. Mar 1995 A
5405235 Lebre et al. Apr 1995 A
5434420 McKeown et al. Jul 1995 A
5440133 Moyers et al. Aug 1995 A
5451794 McKeown et al. Sep 1995 A
5461773 Kawaguchi Oct 1995 A
5463291 Carroll et al. Oct 1995 A
5464411 Schulte et al. Nov 1995 A
5492922 Palkowitz Feb 1996 A
5511549 Legg et al. Apr 1996 A
5521469 Laisne May 1996 A
5538942 Koyama et al. Jul 1996 A
5549616 Schulte et al. Aug 1996 A
5561697 Takafuji et al. Oct 1996 A
5585642 Britton et al. Dec 1996 A
5633747 Nikoonahad May 1997 A
5635721 Bardi et al. Jun 1997 A
5668371 Deasy et al. Sep 1997 A
5672878 Yao Sep 1997 A
5691679 Ackermann et al. Nov 1997 A
5726448 Smith et al. Mar 1998 A
5727554 Kalend et al. Mar 1998 A
5730745 Schulte et al. Mar 1998 A
5751781 Brown et al. May 1998 A
5778047 Mansfield et al. Jul 1998 A
5783914 Hiramoto et al. Jul 1998 A
5784431 Kalend et al. Jul 1998 A
5797924 Schulte et al. Aug 1998 A
5811944 Sampayan et al. Sep 1998 A
5818058 Nakanishi et al. Oct 1998 A
5821705 Caporaso et al. Oct 1998 A
5825845 Blair et al. Oct 1998 A
5841237 Alton Nov 1998 A
5846043 Spath Dec 1998 A
5851182 Sahadevan Dec 1998 A
5866912 Slater et al. Feb 1999 A
5874811 Finlan et al. Feb 1999 A
5895926 Britton et al. Apr 1999 A
5917293 Saito et al. Jun 1999 A
5920601 Nigg et al. Jul 1999 A
5929458 Nemezawa et al. Jul 1999 A
5963615 Egley et al. Oct 1999 A
5993373 Nonaka et al. Nov 1999 A
6008499 Hiramoto et al. Dec 1999 A
6034377 Pu Mar 2000 A
6057655 Jongen May 2000 A
6061426 Linders et al. May 2000 A
6064807 Arai et al. May 2000 A
6066851 Madono et al. May 2000 A
6080992 Nonaka et al. Jun 2000 A
6087670 Hiramoto et al. Jul 2000 A
6094760 Nonaka et al. Aug 2000 A
6118848 Reiffel Sep 2000 A
6140021 Nakasuji et al. Oct 2000 A
6144875 Schweikard et al. Nov 2000 A
6158708 Egley et al. Dec 2000 A
6207952 Kan et al. Mar 2001 B1
6219403 Nishihara Apr 2001 B1
6222905 Yoda et al. Apr 2001 B1
6241671 Ritter et al. Jun 2001 B1
6246066 Yuehu Jun 2001 B1
6256591 Yoda et al. Jul 2001 B1
6265837 Akiyama et al. Jul 2001 B1
6268610 Pu Jul 2001 B1
6278239 Caporaso et al. Aug 2001 B1
6279579 Riaziat et al. Aug 2001 B1
6307914 Kunieda et al. Oct 2001 B1
6316776 Hiramoto et al. Nov 2001 B1
6366021 Meddaugh et al. Apr 2002 B1
6369585 Yao Apr 2002 B2
6380545 Yan Apr 2002 B1
6407505 Bertsche Jun 2002 B1
6417634 Bergstrom Jul 2002 B1
6433336 Jongen et al. Aug 2002 B1
6433349 Akiyama et al. Aug 2002 B2
6433494 Kulish et al. Aug 2002 B1
6441569 Janzow Aug 2002 B1
6443349 Van Der Burg Sep 2002 B1
6465957 Whitham et al. Oct 2002 B1
6472834 Hiramoto et al. Oct 2002 B2
6476403 Dolinskii et al. Nov 2002 B1
6492922 New Dec 2002 B1
6493424 Whitham Dec 2002 B2
6498444 Hanna et al. Dec 2002 B1
6501981 Schweikard et al. Dec 2002 B1
6519316 Collins Feb 2003 B1
6576916 Smith et al. Jun 2003 B2
6593696 Ding et al. Jul 2003 B2
6594336 Nishizawa et al. Jul 2003 B2
6600164 Badura et al. Jul 2003 B1
6617598 Matsuda Sep 2003 B1
6621889 Mostafavi Sep 2003 B1
6639234 Badura et al. Oct 2003 B1
6646383 Bertsche et al. Nov 2003 B2
6670618 Hartmann et al. Dec 2003 B1
6683318 Haberer et al. Jan 2004 B1
6683426 Kleeven Jan 2004 B1
6693283 Eickhoff et al. Feb 2004 B2
6710362 Kraft et al. Mar 2004 B2
6713773 Lyons et al. Mar 2004 B1
6713976 Zumoto et al. Mar 2004 B1
6717162 Jongen Apr 2004 B1
6736831 Hartmann et al. May 2004 B1
6745072 Badura et al. Jun 2004 B1
6769806 Moyers Aug 2004 B2
6774383 Norimine et al. Aug 2004 B2
6777689 Nelson Aug 2004 B2
6777700 Yanagisawa et al. Aug 2004 B2
6780149 Schulte Aug 2004 B1
6799068 Hartmann et al. Sep 2004 B1
6800866 Amemiya et al. Oct 2004 B2
6803591 Yamashita et al. Oct 2004 B2
6814694 Pedroni Nov 2004 B1
6822244 Beloussov et al. Nov 2004 B2
6853142 Chistyakov Feb 2005 B2
6853703 Svatos et al. Feb 2005 B2
6864770 Nemoto et al. Mar 2005 B2
6865254 Nafstadius Mar 2005 B2
6873123 Marchand et al. Mar 2005 B2
6891177 Kraft et al. May 2005 B1
6891924 Yoda et al. May 2005 B1
6894300 Reimoser et al. May 2005 B2
6897451 Kaercher et al. May 2005 B2
6914396 Symons et al. Jul 2005 B1
6936832 Norimine et al. Aug 2005 B2
6953943 Yanagisawa et al. Oct 2005 B2
6965116 Wagner et al. Nov 2005 B1
6969194 Nafstadius Nov 2005 B1
6979832 Yanagisawa et al. Dec 2005 B2
6984835 Harada Jan 2006 B2
6992312 Yanagisawa et al. Jan 2006 B2
6993112 Hesse Jan 2006 B2
7008105 Amann et al. Mar 2006 B2
7011447 Moyers Mar 2006 B2
7012267 Moriyama et al. Mar 2006 B2
7014361 Ein-Gal Mar 2006 B1
7026636 Yanagisawa et al. Apr 2006 B2
7038403 Mastrangeli et al. May 2006 B2
7041479 Swartz et al. May 2006 B2
7045781 Adamec et al. May 2006 B2
7049613 Yanagisawa et al. May 2006 B2
7053389 Yanagisawa et al. May 2006 B2
7054801 Sakamoto et al. May 2006 B2
7060997 Norimine et al. Jun 2006 B2
7071479 Yanagisawa et al. Jul 2006 B2
7073508 Moyers Jul 2006 B2
7081619 Bashkirov et al. Jul 2006 B2
7084410 Beloussov et al. Aug 2006 B2
7091478 Haberer Aug 2006 B2
7102144 Matsuda et al. Sep 2006 B2
7122811 Matsuda et al. Oct 2006 B2
7122966 Norling et al. Oct 2006 B2
7122978 Nakanishi et al. Oct 2006 B2
7135678 Wang et al. Nov 2006 B2
7138771 Bechthold et al. Nov 2006 B2
7154107 Yanagisawa et al. Dec 2006 B2
7154108 Tadokoro et al. Dec 2006 B2
7154991 Earnst et al. Dec 2006 B2
7162005 Bjorkholm Jan 2007 B2
7173264 Moriyama et al. Feb 2007 B2
7173265 Miller et al. Feb 2007 B2
7173385 Caporaso et al. Feb 2007 B2
7186991 Kato et al. Mar 2007 B2
7193227 Hiramoto et al. Mar 2007 B2
7199382 Rigney et al. Apr 2007 B2
7208748 Sliski et al. Apr 2007 B2
7212608 Nagamine et al. May 2007 B2
7212609 Nagamine et al. May 2007 B2
7221733 Takai et al. May 2007 B1
7227161 Matsuda et al. Jun 2007 B2
7247869 Tadokoro et al. Jul 2007 B2
7257191 Sommer Aug 2007 B2
7259529 Tanaka Aug 2007 B2
7262424 Moriyama et al. Aug 2007 B2
7262565 Fujisawa Aug 2007 B2
7274018 Adamec et al. Sep 2007 B2
7280633 Cheng et al. Oct 2007 B2
7295649 Johnsen Nov 2007 B2
7297967 Yanagisawa et al. Nov 2007 B2
7301162 Matsuda et al. Nov 2007 B2
7307264 Brusasco et al. Dec 2007 B2
7317192 Ma Jan 2008 B2
7318805 Schweikard et al. Jan 2008 B2
7319231 Moriyama et al. Jan 2008 B2
7319336 Baur et al. Jan 2008 B2
7331713 Moyers Feb 2008 B2
7332880 Ina et al. Feb 2008 B2
7345291 Kats Mar 2008 B2
7345292 Moriyama et al. Mar 2008 B2
7348557 Armit Mar 2008 B2
7348579 Pedroni Mar 2008 B2
7351988 Naumann et al. Apr 2008 B2
7355189 Yanagisawa et al. Apr 2008 B2
7368740 Beloussov et al. May 2008 B2
7372053 Yamashita et al. May 2008 B2
7378672 Harada May 2008 B2
7381979 Yamashita et al. Jun 2008 B2
7397054 Natori et al. Jul 2008 B2
7397901 Johnsen Jul 2008 B1
7398309 Baumann et al. Jul 2008 B2
7402822 Guertin et al. Jul 2008 B2
7402823 Guertin et al. Jul 2008 B2
7402824 Guertin et al. Jul 2008 B2
7402963 Sliski et al. Jul 2008 B2
7405407 Hiramoto et al. Jul 2008 B2
7425717 Matsuda et al. Sep 2008 B2
7432516 Peggs et al. Oct 2008 B2
7439528 Nishiuchi et al. Oct 2008 B2
7446328 Rigney et al. Nov 2008 B2
7446490 Jongen et al. Nov 2008 B2
7449701 Fujimaki et al. Nov 2008 B2
7453076 Welch et al. Nov 2008 B2
7456415 Yanagisawa et al. Nov 2008 B2
7465944 Ueno et al. Dec 2008 B2
7466085 Nutt Dec 2008 B2
7468506 Rogers et al. Dec 2008 B2
7473913 Hermann et al. Jan 2009 B2
7476867 Fritsch et al. Jan 2009 B2
7476883 Nutt Jan 2009 B2
7482606 Groezinger et al. Jan 2009 B2
7491161 Taguchi Feb 2009 B2
7492556 Atkins et al. Feb 2009 B2
7507975 Mohr Mar 2009 B2
7518108 Frey Apr 2009 B2
7525104 Harada Apr 2009 B2
7541905 Antaya Jun 2009 B2
7547901 Guertin et al. Jun 2009 B2
7554096 Ward et al. Jun 2009 B2
7554097 Ward et al. Jun 2009 B2
7555103 Johnsen Jun 2009 B2
7557358 Ward et al. Jul 2009 B2
7557359 Ward et al. Jul 2009 B2
7557360 Ward et al. Jul 2009 B2
7557361 Ward et al. Jul 2009 B2
7560715 Pedroni Jul 2009 B2
7560717 Matsuda et al. Jul 2009 B2
7567694 Lu et al. Jul 2009 B2
7574251 Lu et al. Aug 2009 B2
7576499 Caporaso et al. Aug 2009 B2
7579603 Birgy et al. Aug 2009 B2
7579610 Grozinger et al. Aug 2009 B2
7582866 Furuhashi et al. Sep 2009 B2
7582885 Katagiri et al. Sep 2009 B2
7582886 Trbojevic Sep 2009 B2
7586112 Chiba et al. Sep 2009 B2
7598497 Yamamoto et al. Oct 2009 B2
7609009 Tanaka et al. Oct 2009 B2
7609809 Kapatoes et al. Oct 2009 B2
7609811 Siljamaki et al. Oct 2009 B1
7615942 Sanders et al. Nov 2009 B2
7626347 Sliski et al. Dec 2009 B2
7627267 Saiki Dec 2009 B2
7629598 Harada Dec 2009 B2
7639853 Olivera et al. Dec 2009 B2
7639854 Schnarr et al. Dec 2009 B2
7643661 Ruchala et al. Jan 2010 B2
7656258 Antaya et al. Feb 2010 B1
7659521 Pedroni Feb 2010 B2
7659528 Uematsu Feb 2010 B2
7668291 Nord et al. Feb 2010 B2
7672429 Urano et al. Mar 2010 B2
7679073 Urano et al. Mar 2010 B2
7682078 Rietzel Mar 2010 B2
7692166 Muraki et al. Apr 2010 B2
7692168 Moriyama et al. Apr 2010 B2
7696499 Miller et al. Apr 2010 B2
7696847 Antaya Apr 2010 B2
7701677 Schultz et al. Apr 2010 B2
7709818 Matsuda et al. May 2010 B2
7710051 Caporaso et al. May 2010 B2
7718982 Sliski et al. May 2010 B2
7728311 Gall Jun 2010 B2
7746978 Cheng et al. Jun 2010 B2
7755305 Umezawa et al. Jul 2010 B2
7759642 Nir Jul 2010 B2
7763867 Birgy et al. Jul 2010 B2
7767988 Kaiser et al. Aug 2010 B2
7770231 Prater et al. Aug 2010 B2
7772577 Saito et al. Aug 2010 B2
7773723 Nord et al. Aug 2010 B2
7773788 Lu et al. Aug 2010 B2
7778488 Nord et al. Aug 2010 B2
7783010 Clayton Aug 2010 B2
7784127 Kuro et al. Aug 2010 B2
7786451 Ward et al. Aug 2010 B2
7786452 Ward et al. Aug 2010 B2
7789560 Moyers Sep 2010 B2
7791051 Beloussov et al. Sep 2010 B2
7796731 Nord et al. Sep 2010 B2
7801269 Cravens et al. Sep 2010 B2
7801270 Nord et al. Sep 2010 B2
7801988 Baumann et al. Sep 2010 B2
7807982 Nishiuchi et al. Oct 2010 B2
7809107 Nord et al. Oct 2010 B2
7812319 Diehl et al. Oct 2010 B2
7812326 Grozinger et al. Oct 2010 B2
7816657 Hansmann et al. Oct 2010 B2
7817778 Nord et al. Oct 2010 B2
7817836 Chao et al. Oct 2010 B2
7834334 Grozinger et al. Nov 2010 B2
7834336 Boeh et al. Nov 2010 B2
7835494 Nord et al. Nov 2010 B2
7835502 Spence et al. Nov 2010 B2
7839972 Ruchala et al. Nov 2010 B2
7839973 Nord et al. Nov 2010 B2
7848488 Mansfield Dec 2010 B2
7857756 Warren et al. Dec 2010 B2
7860216 Jongen et al. Dec 2010 B2
7860550 Saracen et al. Dec 2010 B2
7868301 Diehl Jan 2011 B2
7875861 Huttenberger et al. Jan 2011 B2
7875868 Moriyama et al. Jan 2011 B2
7881431 Aoi et al. Feb 2011 B2
7894574 Nord et al. Feb 2011 B1
7906769 Blasche et al. Mar 2011 B2
7914734 Livingston Mar 2011 B2
7919765 Timmer Apr 2011 B2
7920040 Antaya et al. Apr 2011 B2
7920675 Lomax et al. Apr 2011 B2
7928415 Bert et al. Apr 2011 B2
7934869 Ivanov et al. May 2011 B2
7940881 Jongen et al. May 2011 B2
7943913 Balakin May 2011 B2
7947969 Pu May 2011 B2
7949096 Cheng et al. May 2011 B2
7950587 Henson et al. May 2011 B2
7960710 Kruip et al. Jun 2011 B2
7961844 Takeda et al. Jun 2011 B2
7977648 Westerly et al. Jul 2011 B2
7977656 Fujimaki et al. Jul 2011 B2
7977657 Flynn et al. Jul 2011 B2
7982198 Nishiuchi et al. Jul 2011 B2
7982416 Tanaka et al. Jul 2011 B2
7984715 Moyers Jul 2011 B2
7986768 Nord et al. Jul 2011 B2
7987053 Schaffner Jul 2011 B2
7989785 Emhofer et al. Aug 2011 B2
7990524 Jureller et al. Aug 2011 B2
7997553 Sloan et al. Aug 2011 B2
8002466 Von Neubeck et al. Aug 2011 B2
8003964 Stark et al. Aug 2011 B2
8009803 Nord et al. Aug 2011 B2
8009804 Siljamaki et al. Aug 2011 B2
8039822 Rietzel Oct 2011 B2
8041006 Boyden et al. Oct 2011 B2
8044364 Yamamoto Oct 2011 B2
8049187 Tachikawa Nov 2011 B2
8053508 Korkut et al. Nov 2011 B2
8053739 Rietzel Nov 2011 B2
8053745 Moore Nov 2011 B2
8053746 Timmer et al. Nov 2011 B2
8063381 Tsoupas et al. Nov 2011 B2
8067748 Balakin Nov 2011 B2
8069675 Radovinsky et al. Dec 2011 B2
8071966 Kaiser et al. Dec 2011 B2
8080801 Safai Dec 2011 B2
8085899 Nord et al. Dec 2011 B2
8089054 Balakin Jan 2012 B2
8093564 Balakin Jan 2012 B2
8093568 Mackie et al. Jan 2012 B2
8111125 Antaya et al. Feb 2012 B2
8129699 Balakin Mar 2012 B2
8144832 Balakin Mar 2012 B2
8153989 Tachikawa et al. Apr 2012 B2
8173981 Trbojevic May 2012 B2
8188688 Balakin May 2012 B2
8198607 Balakin Jun 2012 B2
8222613 Tajiri et al. Jul 2012 B2
8227768 Smick et al. Jul 2012 B2
8232536 Harada Jul 2012 B2
8288742 Balakin Oct 2012 B2
8291717 Radovinsky et al. Oct 2012 B2
8294127 Tachibana Oct 2012 B2
8304725 Komuro et al. Nov 2012 B2
8304750 Preikszas et al. Nov 2012 B2
8309941 Balakin Nov 2012 B2
8330132 Guertin et al. Dec 2012 B2
8334520 Otaka et al. Dec 2012 B2
8335397 Takane et al. Dec 2012 B2
8344340 Gall et al. Jan 2013 B2
8350214 Otaki et al. Jan 2013 B2
8368038 Balakin Feb 2013 B2
8368043 Havelange et al. Feb 2013 B2
8373143 Balakin Feb 2013 B2
8373145 Balakin Feb 2013 B2
8373146 Balakin Feb 2013 B2
8378299 Frosien Feb 2013 B2
8378321 Balakin Feb 2013 B2
8382943 Clark Feb 2013 B2
8389949 Harada et al. Mar 2013 B2
8399866 Balakin Mar 2013 B2
8405042 Honda et al. Mar 2013 B2
8405056 Amaldi Mar 2013 B2
8415643 Balakin Apr 2013 B2
8416918 Nord et al. Apr 2013 B2
8421041 Balakin Apr 2013 B2
8426833 Trbojevic Apr 2013 B2
8436323 Iseki et al. May 2013 B2
8440987 Stephani et al. May 2013 B2
8445872 Behrens et al. May 2013 B2
8466441 Iwata et al. Jun 2013 B2
8472583 Star-Lack et al. Jun 2013 B2
8483357 Siljamaki et al. Jul 2013 B2
8487278 Balakin Jul 2013 B2
8552406 Phaneuf et al. Oct 2013 B2
8552408 Hanawa et al. Oct 2013 B2
8569717 Balakin Oct 2013 B2
8575563 Cameron et al. Nov 2013 B2
8581215 Balakin Nov 2013 B2
8581523 Gall Nov 2013 B2
8581525 Antaya et al. Nov 2013 B2
8637833 Balakin Jan 2014 B2
8653314 Pelati et al. Feb 2014 B2
8653473 Yajima Feb 2014 B2
8766218 Jongen Jul 2014 B2
8791435 Balakin Jul 2014 B2
8901509 Balakin Dec 2014 B2
8905908 Matsuguma Dec 2014 B2
8907311 Gall et al. Dec 2014 B2
8952634 Sliski Feb 2015 B2
8963112 Balakin Feb 2015 B1
8970137 Gall Mar 2015 B2
8975816 Scheitrum et al. Mar 2015 B2
9012866 Benna et al. Apr 2015 B2
9028384 Iikura May 2015 B2
9044600 Balakin Jun 2015 B2
9056199 Balakin Jun 2015 B2
9176468 Ueno Nov 2015 B2
9451688 Jongen Sep 2016 B2
9452301 Gall et al. Sep 2016 B2
20020172317 Maksimchuk et al. Nov 2002 A1
20030048080 Amemiya et al. Mar 2003 A1
20030125622 Schweikard et al. Jul 2003 A1
20030136924 Kraft et al. Jul 2003 A1
20030146759 Bashkirov Aug 2003 A1
20030152197 Moyers Aug 2003 A1
20030163015 Yanagisawa et al. Aug 2003 A1
20030183779 Norimine et al. Oct 2003 A1
20030234369 Glukhoy Dec 2003 A1
20040000650 Yanagisawa et al. Jan 2004 A1
20040017888 Seppi et al. Jan 2004 A1
20040056212 Yanagisawa et al. Mar 2004 A1
20040061077 Muramatsu et al. Apr 2004 A1
20040061078 Muramatsu et al. Apr 2004 A1
20040085023 Chistyakov May 2004 A1
20040098445 Baumann et al. May 2004 A1
20040111134 Muramatsu et al. Jun 2004 A1
20040118081 Reimoser et al. Jun 2004 A1
20040149934 Yanagisawa et al. Aug 2004 A1
20040159795 Kaercher et al. Aug 2004 A1
20040173763 Moriyama et al. Sep 2004 A1
20040174958 Moriyama et al. Sep 2004 A1
20040183033 Moriyama et al. Sep 2004 A1
20040183035 Yanagisawa et al. Sep 2004 A1
20040200982 Moriyama et al. Oct 2004 A1
20040200983 Fujimaki et al. Oct 2004 A1
20040213381 Harada Oct 2004 A1
20040227104 Matsuda et al. Nov 2004 A1
20040232356 Norimine et al. Nov 2004 A1
20040240626 Moyers Dec 2004 A1
20050058245 Ein-Gal Mar 2005 A1
20050089141 Brown Apr 2005 A1
20050161618 Pedroni Jul 2005 A1
20050184686 Caporaso et al. Aug 2005 A1
20050228255 Saracen et al. Oct 2005 A1
20050234327 Saracen et al. Oct 2005 A1
20050238134 Brusasco et al. Oct 2005 A1
20050247890 Norimine et al. Nov 2005 A1
20060017015 Sliski et al. Jan 2006 A1
20060067468 Rietzel Mar 2006 A1
20060126792 Li Jun 2006 A1
20060145088 Ma Jul 2006 A1
20060170381 Amaldi et al. Aug 2006 A1
20060173294 Ein-Gal Aug 2006 A1
20060175991 Fujisawa Aug 2006 A1
20060273264 Nakayama et al. Dec 2006 A1
20060284562 Hruby et al. Dec 2006 A1
20070001128 Sliski et al. Jan 2007 A1
20070013273 Albert et al. Jan 2007 A1
20070014654 Haverfield et al. Jan 2007 A1
20070023699 Yamashita et al. Feb 2007 A1
20070029510 Hermann et al. Feb 2007 A1
20070051904 Kaiser et al. Mar 2007 A1
20070061937 Curle Mar 2007 A1
20070092812 Caporaso et al. Apr 2007 A1
20070114945 Mattaboni et al. May 2007 A1
20070133752 Ein-Gal Jun 2007 A1
20070145916 Caporaso et al. Jun 2007 A1
20070170994 Peggs et al. Jul 2007 A1
20070171015 Antaya Jul 2007 A1
20070181519 Khoshnevis Aug 2007 A1
20070252093 Fujimaki et al. Nov 2007 A1
20070284548 Kaiser et al. Dec 2007 A1
20080067452 Moriyama et al. Mar 2008 A1
20080078937 Tsuchiya et al. Apr 2008 A1
20080093567 Gall Apr 2008 A1
20080218102 Sliski et al. Sep 2008 A1
20080234531 Welch Sep 2008 A1
20080270517 Baumann et al. Oct 2008 A1
20090096179 Stark et al. Apr 2009 A1
20090101832 Diehl Apr 2009 A1
20090140671 O'Neal, III Jun 2009 A1
20090140672 Gall Jun 2009 A1
20090200483 Gall et al. Aug 2009 A1
20090230299 Shichi et al. Sep 2009 A1
20090236545 Timmer Sep 2009 A1
20090296885 Boeh et al. Dec 2009 A1
20090309046 Balakin Dec 2009 A1
20090314960 Balakin Dec 2009 A1
20090321665 Timmer Dec 2009 A1
20100006770 Balakin Jan 2010 A1
20100027745 Balakin Feb 2010 A1
20100038552 Trbojevic Feb 2010 A1
20100045213 Sliski et al. Feb 2010 A1
20100046697 Balakin Feb 2010 A1
20100051833 Guertin et al. Mar 2010 A1
20100192303 Miller et al. Aug 2010 A1
20100209335 Mills Aug 2010 A1
20100230617 Gall Sep 2010 A1
20100308235 Sliski et al. Dec 2010 A1
20110006212 Shchory Jan 2011 A1
20110220809 Yajima et al. Sep 2011 A1
20110233423 Balakin Sep 2011 A1
20110240874 Iwata Oct 2011 A1
20110284760 Balakin Nov 2011 A1
20110299919 Stark et al. Dec 2011 A1
20120014501 Pelc et al. Jan 2012 A1
20120081041 Cheung et al. Apr 2012 A1
20120126140 Gall et al. May 2012 A1
20120217903 Tanaka Aug 2012 A1
20120313003 Trbojevic Dec 2012 A1
20130053616 Gall et al. Feb 2013 A1
20130127375 Sliski et al. May 2013 A1
20130131424 Sliski et al. May 2013 A1
20130237425 Leigh et al. Sep 2013 A1
20130249443 Antaya Sep 2013 A1
20140028220 Bromberg et al. Jan 2014 A1
20140042934 Tsutsui Feb 2014 A1
20140062344 Gall Mar 2014 A1
20140094643 Gall et al. Apr 2014 A1
20140097920 Goldie et al. Apr 2014 A1
20150009917 Cho et al. Jan 2015 A1
20150009918 Yeoum et al. Jan 2015 A1
20150161793 Takahashi Jun 2015 A1
20170028224 Gall et al. Feb 2017 A1
Foreign Referenced Citations (181)
Number Date Country
2005267078 Feb 2006 AU
2629333 May 2007 CA
1377521 Oct 2002 CN
1537657 Oct 2004 CN
1631061 Jun 2005 CN
101061759 Oct 2007 CN
101361156 Feb 2009 CN
101932361 Dec 2010 CN
101933405 Dec 2010 CN
101933406 Dec 2010 CN
102036461 Apr 2011 CN
102172106 Aug 2011 CN
104244562 Dec 2014 CN
104812443 Jul 2015 CN
104812444 Jul 2015 CN
104822417 Aug 2015 CN
2753397 Jun 1978 DE
3148100 Jun 1983 DE
3530446 Mar 1986 DE
4101094 May 1992 DE
4411171 Oct 1995 DE
0044153 Jan 1982 EP
0194728 Sep 1986 EP
0208163 Jan 1987 EP
0221987 May 1987 EP
0222786 May 1987 EP
0276123 Jul 1988 EP
0277521 Aug 1988 EP
0306966 Mar 1989 EP
0388123 Sep 1990 EP
0465597 Jan 1992 EP
0499253 Aug 1992 EP
0776595 Jun 1997 EP
0864337 Sep 1998 EP
0911064 Apr 1999 EP
1069809 Jan 2001 EP
1153398 Nov 2001 EP
1265462 Dec 2002 EP
1294445 Mar 2003 EP
1348465 Oct 2003 EP
1358908 Nov 2003 EP
1371390 Dec 2003 EP
1402923 Mar 2004 EP
1430932 Jun 2004 EP
1454653 Sep 2004 EP
1454654 Sep 2004 EP
1454655 Sep 2004 EP
1454656 Sep 2004 EP
1454657 Sep 2004 EP
1477206 Nov 2004 EP
1605742 Dec 2005 EP
1738798 Jan 2007 EP
1790203 May 2007 EP
1826778 Aug 2007 EP
1949404 Jul 2008 EP
2026640 Feb 2009 EP
2183753 May 2010 EP
2227295 Sep 2010 EP
2232961 Sep 2010 EP
2232962 Sep 2010 EP
2259664 Dec 2010 EP
2363170 Sep 2011 EP
2363171 Sep 2011 EP
2394498 Dec 2011 EP
2814304 Dec 2014 EP
2900324 Aug 2015 EP
2900325 Aug 2015 EP
2900326 Aug 2015 EP
2560421 Aug 1985 FR
2911843 Aug 2008 FR
0957342 May 1964 GB
1360085 Jul 1974 GB
1485329 Sep 1977 GB
2015821 Sep 1979 GB
1583400 Jan 1981 GB
2361523 Oct 2001 GB
61-225798 Oct 1986 JP
10247600 Sep 1989 JP
4-94198 Mar 1992 JP
04-128717 Apr 1992 JP
04-129768 Apr 1992 JP
04-273409 Sep 1992 JP
04-337300 Nov 1992 JP
05-341352 Dec 1993 JP
10270200 Oct 1998 JP
11-47287 Feb 1999 JP
11-243295 Sep 1999 JP
2000-243309 Sep 2000 JP
2000-294399 Oct 2000 JP
2001-6900 Jan 2001 JP
2001-006900 Jan 2001 JP
2001-009050 Jan 2001 JP
2001-129103 May 2001 JP
2001-346893 Dec 2001 JP
2002-164686 Jun 2002 JP
2003-504628 Feb 2003 JP
2003-517755 May 2003 JP
2004-139944 May 2004 JP
2005-526578 Sep 2005 JP
2006-032282 Feb 2006 JP
2006233831 Sep 2006 JP
2007260939 Oct 2007 JP
2007-319439 Dec 2007 JP
2008-012121 Jan 2008 JP
2008-507826 Mar 2008 JP
2008-089341 Apr 2008 JP
2008-270039 Nov 2008 JP
2009-515671 Apr 2009 JP
2009-516905 Apr 2009 JP
43-23267 Sep 2009 JP
2010-204020 Sep 2010 JP
2010-536130 Nov 2010 JP
2011-505191 Feb 2011 JP
2011-505670 Feb 2011 JP
2011-507151 Mar 2011 JP
2011-521425 Jul 2011 JP
2011-210494 Oct 2011 JP
2011-224342 Nov 2011 JP
05-046928 Oct 2012 JP
300137 Nov 1969 SU
569635 Aug 1977 SU
569635 Aug 1977 SU
200930160 Jul 2009 TW
200934682 Aug 2009 TW
200939908 Sep 2009 TW
200940120 Oct 2009 TW
201422278 Jun 2014 TW
201422279 Jun 2014 TW
201424466 Jun 2014 TW
201429514 Aug 2014 TW
201433331 Sep 2014 TW
201434508 Sep 2014 TW
201438787 Oct 2014 TW
WO-8607229 Dec 1986 WO
WO-9012413 Oct 1990 WO
WO-9203028 Feb 1992 WO
WO-9302536 Feb 1993 WO
WO-9817342 Apr 1998 WO
WO-9939385 Aug 1999 WO
WO-0040064 Jul 2000 WO
WO-0049624 Aug 2000 WO
WO-0126230 Apr 2001 WO
WO-0126569 Apr 2001 WO
WO-0207817 Jan 2002 WO
WO-03039212 May 2003 WO
WO-03092340 Nov 2003 WO
WO-03092812 Nov 2003 WO
WO-2004026401 Apr 2004 WO
WO-2004101070 Nov 2004 WO
WO-2005102453 Nov 2005 WO
WO-2006012452 Feb 2006 WO
WO-2006012467 Feb 2006 WO
WO2007061937 May 2007 WO
WO-2007061937 May 2007 WO
WO-2007084701 Jul 2007 WO
WO-2007130164 Nov 2007 WO
WO-2007145906 Dec 2007 WO
WO-2008030911 Mar 2008 WO
WO-2008081480 Jul 2008 WO
WO-2009048745 Apr 2009 WO
WO-2009056165 May 2009 WO
WO-2009070173 Jun 2009 WO
WO-2009070588 Jun 2009 WO
WO-2009073480 Jun 2009 WO
WO-2009080080 Jul 2009 WO
WO-2010089574 Aug 2010 WO
WO2010149740 Dec 2010 WO
WO-2010149740 Dec 2010 WO
WO-2012044957 Apr 2012 WO
WO-2012071142 May 2012 WO
WO-2013079311 Jun 2013 WO
WO-2013098089 Jul 2013 WO
WO-2013142409 Sep 2013 WO
WO-2014018876 Jan 2014 WO
WO-2014052708 Apr 2014 WO
WO2014052709 Apr 2014 WO
WO 2014052716 Apr 2014 WO
WO-2014052718 Apr 2014 WO
WO-2014052719 Apr 2014 WO
WO-2014052721 Apr 2014 WO
WO-2014052722 Apr 2014 WO
Non-Patent Literature Citations (394)
Entry
US 8,581,524, 11/2013, O'Neal et al. (withdrawn)
Tilly, et al., “Development and verification of the pulsed scanned proton beam at The Svedberg Laboratory in Uppsala”, Physics in Medicine and Biology, Phys. Med. Biol. 52, pp. 2741-2454, 2007.
U.S. Appl. No. 14/039,342, Corresponding PCT Appln. No. PCT/US2013/062117, Corresponding Provisional U.S. Appl. No. 61/707,515.
U.S. Appl. No. 14/039,073, Corresponding PCT Appln. No. PCT/US2013/062102, Corresponding Provisional U.S. Appl. No. 61/707,548.
U.S. Appl. No. 14/039,084, Corresponding PCT Appln. No. PCT/US2013/062120, Corresponding Provisional U.S. Appl. No. 61/707,572.
U.S. Appl. No. 14/039,652, Corresponding PCT Appln. No. PCT/US2013/062112, Corresponding Provisional U.S. Appl. No. 61/707,590.
U.S. Appl. No. 14/039,752, Corresponding PCT Appln. No. PCT/US2013/062116, Corresponding Provisional U.S. Appl. No. 61/707,704.
U.S. Appl. No. 14/038,888, Corresponding PCT Appln. No. PCT/US2013/062137, Corresponding Provisional U.S. Appl. No. 61/707,624.
U.S. Appl. No. 14/038,967, Corresponding PCT Appln. No. PCT/US2013/062119, Corresponding Provisional U.S. Appl. No. 61/707,645.
U.S. Appl. No. 13/916,401.
U.S. Appl. No. 13/907,601.
U.S. Appl. No. 13/780,118, Corresponding Provisional U.S. Appl. No. 61/605,690.
Corresponding Provisional U.S. Appl. No. 61/883,631.
International Search Report and Written Opinion from corresponding PCT application No. PCT/US2013/062103 mailed Apr. 14, 2014 (14 pages).
Office Action for JP2015-534721, 14 pages (Feb. 3, 2016) (in both Japanese and English).
First Office Action for 201380062111.9, 46 pages (dated Jun. 1, 2016).
Second Office Action (English) for JP2015-534721, 5 pages (dated Dec. 26, 2016).
Second Office Action (Japanese) for JP2015-534721, 5 pages (dated Dec. 26, 2016).
File History of Reissue U.S. Appl. No. 15/429,078 (downloaded Mar. 13, 2017).
“The Cutting Edge of Cancer Therapy Using Proton Beams,” The Journal of Practical Pharmacy, vol. 46, No. 1, 10 pages (1995). [Japanese] (English Abstract).
18th Japan Conference on Radiation and Radioisotopes [Japanese], Nov. 25-27, 1987, 9 pages.
510(k) Summary: Ion Beam Applications S.A., FDA, Jul. 12, 2001, 5 pages.
510(k) Summary: Optivus Proton Beam Therapy System, Jul. 21, 2000, 5 pages.
Abrosimov et al., 1000MeV Proton Beam Therapy facility at Petersburg Nuclear Physics Institute Synchrocyclotron, Medical Radiology (Moscow) 32, 10 (1987) revised in Journal of Physics, Conference Series 41, 2006, pp. 424-432, Institute of Physics Publishing Limited.
Abrosimov et al., Neutron Time-of-flight Spectrometer Gneis at the Gatchina 1 GeV Protron Syncrhocyclotron, Mar. 9, 1985 and revised form Jul. 31, 1985, Lemingrad Nuclear Physics Institute, Gatchina, 188350, USSR (15 pages).
Adachi et al., A 150MeV FFAG Synchrotron with Return-Yoke Free Magent, Proceedings of the 2001 Particle Accelerator Conference, Chicago, 2001, 3 pages.
Ageyev et al., The IHEP Accelerating and Storage Complex (UNK) Status Report, 11th International Conference on High-Energy Accelerators, 1980, pp. 60-70.
Agosteo et al., Maze Design of a gantry room for proton therapy, Nuclear Instruments & Methods In Physics Research, 1996, Section A, 382, pp. 573-582.
Alexeev et al., R4 Design of Superconducting Magents for Proton Synchrotrons, Proceedings of the Fifth International Cryogenic Engineering Conference, 197 4, pp. 531-533.
Allardyce et al., Performance and Prospects of the Reconstructed CERN 600 MeV Synchrocyclotron, IEEE Transactions on Nuclear Science USA, Jun. 1977, ns-24:(3) 1631-1633.
Alonso, Magnetically Scanned Ion Beams for Radiation Therapy, Accelerator & Fusion Research Division, Lawrence Berkeley Laboratory, Berkeley, CA, Oct. 1988, 13 pages.
Amaldi et al., The Italian project for a hadrontherapy centre Nuclear Instruments and Methods in Physics Research A, 1995, 360, pp. 297-301.
Amaldi, Cyclinacs, Novel Fast-Cycling Accelerators for Hadrontherapy, 2007, Cyclotrons and Their Applications, 18th International Conference, pp. 166-168.
Amaldi, Overview of the world landscape of Hadrontherapy and the projects of the TERA foundation, Physica Medica, An International journal Devoted to the Applications of Physics to Medicine and Biology, Jul. 1998, vol. XIV, Supplement 1, 6th Workshop on Heavy Charged Particles in Biology and Medicine, Instituto Scientific Europeo (ISE), Sep. 29-Oct. 1, 1977, Baveno, pp. 76-85.
An Accelerated Collaboration Meets with Beaming Success, Lawrence Livermore National Laboratory, Apr. 12, 2006, S&TR, Livermore, California, pp. 1-3, http://www.llnl.gov/str/Apri106/Caporaso.html.
Anferov et al., Status of the Midwest Proton Radiotherapy Institute, Proceedings of the 2003 Particle Accelerator Conference, 2003, pp. 699-701.
Anferov et al., The Indiana University Midwest Proton Radiation Institute, Proceedings of the 2001 Particle Accelerator Conference, 2001, Chicago, pp. 645-647.
Appun, Various problems of magnet fabrication for high-energy accelerators, Journal for All Engineers Interested in the Nuclear Field, 1967, 11 pages 10-16 (1967) [Lang.: German], English bibliographic information (httn://www.osti.1mv/enernvcitations/nroduct.biblio.isn?ostiid=4442292).
Arduini et al. Physical specifications of clinical proton beams from a synchrotron, Med. Phys, Jun. 1996, 23 ( 6): 939-951.
Badano et al., Proton-Ion Medical Machine Study (PIMMS) Part I, PIMMS, Jan. 1999, 238 pages.
Beam Delivery and Properties, Journal of the ICRU, 2007, 7(2):20 pages.
Beeckman et al., Preliminary design of a reduced cost proton therapy facility using a compact, high field isochronous cyclotron, Nuclear Instruments and Methods in Physics Research B56/57, 1991, pp. 1201-1204.
Bellomo et al., The Superconducting Cyclotron Program at Michigan State University, Bulletin of the American Physical Society, Sep. 1980, 25(7):767.
Benedikt and Carli, Matching to Gantries for Medical Synchrotrons IEEE Proceedings of the 1997 Particle Accelerator Conference, 1997, pp. 13 79-13 81.
Bieth et al., A Very Compact Protontherapy Facility Based on an Extensive Use of High Temperature Superconductors (HTS) Cyclotrons and their Applications 1998, Proceedings of the Fifteenth International Conference on Cyclotrons and their Applications, Caen, Jun. 14-19, 1998, pp. 669-672.
Bigham, Magnetic Trim Rods for Superconducting Cyclotrons, Nuclear Instruments and Methods (North-Holland Publishing Co.), 1975, 141:223-228.
Bimbot, First Studies of the External Beam from the Orsay S.C. 200 MeV, Institut de Physique Nucleaire, BP 1, Orsay, France, IEEE, 1979, pp. 1923-1926.
Blackmore et al., Operation of the Triumf Proton Therapy Facility, IEEE Proceedings of the 1997 Particle Accelerator Conference, May 12-16, 1997, 3:3831-3833.
Bloch, The Midwest Proton Therapy Center, Application of Accelerators in Research and Industry, Proceedings of the Fourteenth Int'l. Conf, Part Two, Nov. 1996, pp. 1253-1255.
Blom, Mikael, Development of a Scanning System for Proton Therapy in Uppsala, Department of Radiation Sciences, Uppsala University, 2450-2451.
Blosser et al., A Compact Superconducting Cyclotron for the Production of High Intensity Protons, Proceedings of the 1997 Particle Accelerator Conference, May 12-16, 1997, 1:1054-1056.
Blosser et al., Advances in Superconducting Cyclotrons at Michigan State University, Proceedings of the 11th International Conference on Cyclotrons and their Applications, Oct. 1986, pp. 157-167, Tokyo.
Blosser et al., Characteristics of a 400 (Q2/A) MeV Super-Conducting Heavy-Ion Cyclotron, Bulletin of the American Physical Society, Oct. 1974, p. 1026.
Blosser et al., Medical Accelerator Projects at Michigan State Univ. IEEE Proceedings of the 1989 Particle Accelerator Conference, Mar. 20-23, 1989, 2:742-746.
Blosser et al., Problems and Accomplishments of Superconducting Cyclotrons, Proceedings of the 14th International Conference, Cyclotrons and Their Applications, Oct. 1995, pp. 674-684.
Blosser et al., Progress toward an experiment to study the effect of RF grounding in an internal ion source on axial oscillations of the beam in a cyclotron, National Superconducting Cyclotron Laboratory, Michigan State University, Report MSUCL-760, CP600, Cyclotrons and their Applications 2011, Sixteenth International Conference, 2001, pp. 274-276.
Blosser et al., Superconducting Cyclotron for Medical Application, IEEE Transactions on Magnetics, Mar. 1989, 25(2): 1746-1754.
Blosser et al., Superconducting Cyclotrons, Seventh International Conference on Cyclotrons and their Applications, Aug. 19-22, 1975, pp. 584-594.
Blosser, Application of Superconductivity in Cyclotron Construction, Ninth International Conference on Cyclotrons and their Applications, Sep. 1981, pp. 147-157.
Blosser, Applications of Superconducting Cyclotrons, Twelfth International Conference on Cyclotrons and Their Applications, May 8-12, 1989, pp. 137-144.
Blosser, Future Cyclotrons, AIP, The Sixth International Cyclotron Conference, 1972, pp. 16-32.
Blosser, H. G. “Compact Superconducting Synchrocyclotron Systems for Proton Therapy,” Nuclear Instruments & Methods in Physics Research, Section B40-41, Part II, pp. 1326-1330 (1989).
Blosser, H., Present and Future Superconducting Cyclotrons, Bulletin of the American Physical Society, Feb. 1987, 32(2):171 Particle Accelerator Conference, Washington, D.C.
Blosser, H.G., “Progress on the Coupled Superconducting Cyclotron Project,” Bulletin of the American Physical Society, vol. 26, No. 4, p. 558 (Apr. 1981).
Blosser, H.G., Superconducting Cyclotrons at Michigan State University, Nuclear Instruments & Methods in Physics Research, 1987,vol. B 24/25, part II, pp. 752-756.
Blosser, Medical Cyclotrons, Physics Today, Special Issue Physical Review Centenary, Oct. 1993, pp. 70-73.
Blosser, Preliminary Design Study Exploring Building Features Required for a Proton Therapy Facility for the Ontario Cancer Institute, Mar. 1991, MSUCL-760a, 53 pages.
Blosser, Synchrocyclotron Improvement Programs, IEEE Transactions on Nuclear Science USA, Jun. 1969, 16(3):Part I, pp. 405-414.
Blosser, The Michigan State University Superconducting Cyclotron Program, Nuclear Science, Apr. 1979, NS-26(2):2040-2047.
Botha et al., A New Multidisciplinary Separated-Sector Cyclotron Facility, IEEE Transactions on Nuclear Science, 1977, NS-24(3): 1118-1120.
Canadian Office action from Canadian application No. 2,629,333 dated Aug. 30, 2010 (5 pages).
Canadian Office action from Canadian application No. 2,629,333 dated May 11, 2011 (2 pages).
Canadian office action from Canadian application No. 2574122 dated Aug. 14, 2014 (6 pages).
Chichili et al., Fabrication ofNb3Sn Shell-Type Coils with Pre-Preg Ceramic Insulation, American Institute of Physics Conference Proceedings, AIP USA, No. 711, (XP-002436709, ISSN: 0094-243X), 2004, pp. 450-457.
Chinese Office action from Chinese application No. 200680051421.0 dated Aug. 22, 2011 (4 pages).
Chinese Office action from Chinese application No. 200680051421.0 dated Dec. 25, 2009 (8 pages).
Chinese Office action from Chinese application No. 200680051421.0 dated Mar. 21, 2011 (6 pages).
Chinese Office Action from Chinese Application No. 200780102281.X dated Dec. 7, 2011 with English translation (23 pages).
Chinese Office action from Chinese application No. 200880125832.9, dated Jun. 5, 2012 (5 pages).
Chinese Office action from Chinese application No. 200880125832.9, dated Sep. 22, 2011 (11 pages).
Chinese Office action from Chinese application No. 200880125918.1, dated Sep. 15, 2011 (17 pages).
Chinese Office action with English translation from Chinese Application No. 200880125832.9, dated Mar. 4, 2013 (8 pages).
Chong et al., Radiology Clinic North American 7, 3319, 1969, 27 pages.
Chu et al., Instrumentation for Treatment of Cancer Using Proton and Light-ion Beams, Review of Scientific Instruments, Aug. 1993, 64 (8):2055-2122.
Chu et al., Performance Specifications for Proton Medical Facility, Lawrence Berkeley Laboratory, University of California, Mar. 1993, 128 pages.
Chu, Instrumentation in Medical Systems, Accelerator and Fusion Research Division, Lawrence Berkeley Laboratory, University of California, Berkeley, CA, May 1995, 9 pages.
Cohen, R. et al., Nevis Synchrocyclotron Conversion Project, IEEE Transactions on Nuclear Science, IEEE Service Center, New York, NY, US, vol. 16, No. 3, Jun. 1, 1969, pp. 421-425, XP011351570, ISSN: 0018-9499, DOI: 10.1109/TNS.1969.4325264 abstract; figures I-4a Chap. 1, p. 421-2; chap. 11 from p. 423, col. 2 to p. 425, col. 1. (5 pages).
Cole et al., Design and Application of a Proton Therapy Accelerator, Fermi National Accelerator Laboratory, IEEE, 1985, 5 pages.
Collins, et al., The Indiana University Proton Therapy System, Proceedings of EPAC 2006, Edinburgh, Scotland, 2006, 3 pages.
Conradi et al., Proposed New Facilities for Proton Therapy at iThemba Labs, Proceedings of EPAC, 2002, pp. 560-562.
C/E Source of Ions for Use in Sychro-Cyclotrons Search, Jan. 31, 2005, 9 pages.
Source Search Cites of U.S. And Foreign Patents/Published applications in the name of Mitsubishi Denki Kabushiki Kaisha and Containing the Keywords (Proton and Synchrocyclotron), Jan. 2005, 8 pages.
Cosgrove et al., Microdosimetric Studies on the Orsay Proton Synchrocyclotron at 73 and 200 MeV, Radiation Protection Dosimetry, 1997, 70(1-4):493-496.
Coupland, High-field (5 T) pulsed superconducting dipole magnet, Proceedings of the Institution of Electrical Engineers, Jul. 1974, 121(7):771-778.
Coutrakon et al. Proton Synchrotrons for Cancer Therapy, Application of Accelerators in Research and Industry—Sixteenth International Conf., American Institute of Physics, Nov. 1-5, 2000, vol. 576, pp. 861-864.
Coutrakon et al., A prototype beam delivery system for the proton medical accelerator at Loma Linda, Medical Physics, Nov./Dec. 1991, 18(6):1093-1099.
CPAC Highlights Its Proton Therapy Program at ESTRO Annual Meeting, TomoTherapy Incorporated, Sep. 18, 2008, Madison, Wisconsin, pp. 1-2.
Cuttone, Applications of a Particle Accelerators in Medical Physics, Istituto Nazionale di Fisica Nucleare-Laboratori Nazionali del Sud, V.S. Sofia, 44 Cantania, Italy, Jan. 2010, 17 pages.
Dahl P, Superconducting Magnet System, American Institute of Physics, AIP Conference Proceedings, 1987-1988, 2: 1329-1376.
Dey, M.K., et al., Coil Centering for the Kolkata Superconducting Cyclotron Magnet, Cyclotrons and their applications, Proceedings, 18th International Conference, Cyclotrons 2007, Giardini Naxo, Italy, Oct. 1-5, 2007 (3 pages).
Dialog Search, Jan. 31, 2005, 17 pages.
Dugan et al., Tevatron Status IEEE, Particle Accelerator Conference, Accelerator Science & Technology, 1989, pp. 426-430.
Eickhoff et al., The Proposed Accelerator Facility for Light Ion Cancer Therapy in Heidelberg, Proceedings of the 1999 Particle Accelerator Conference, New York, 1999, pp. 2513-2515.
Elo, Don, et al., Mechanical Design of Regenerative Deflector for the Berkeley 88-Inch Cyclotron, Proceedings of the International Conference on Isochronous Cyclotrons, Gatlinburg, Tennessee, Aug. 1966 (7 pages).
Enchevich et al., Minimizing Phase Losses in the 680 MeV Synchrocyclotron by Correcting the Accelerating Voltage Amplitude, Atomnava Energiva, 1969, 26:(3):315-316.
Endo et al., Compact Proton and Carbon Ion Synchrotrons for Radiation Therapy, Proceedings of EPAC 2002, Paris France, 2002, pp. 2733-2735.
English translation of Chinese Office action from Chinese application No. 200880125832.9, dated Jun. 5, 2012 (5 pages).
European Communication from European application No. 06838033.6 dated Apr. 20, 2010 (7 pages).
European Communication from European application No. 07868958.5, dated Nov. 26, 2010 (50 pages).
European Communication from European application No. 11165423.2 dated Sep. 2, 2011 (5 pages).
European Communication from European application No. 13774886.9 dated Jun. 12, 2015 (2 pages).
European Communication issued in European Application No. 05776532.3 dated Jun. 10, 2011 (10 pages).
European Communication issued in European application No. 13774886.9 dated Jun. 12, 2015, with amended claims filed on Jun. 12, 2015 (20 pages).
European Communication issued in European application No. 13783422.2 dated Jun. 12, 2015 (2 pages).
European Patent Office communication for application No. 06838033.6, patent No. 1949404, dated Aug. 5, 2009 (1 page).
European Patent Office communication from European application No. 07868958.5, dated Jul. 16, 2010 (2 pages).
European Patent Office communication from European application No. 08855024.9, dated Jul. 30, 2010 (2 pages).
European Search Report from application No. EP 06838033.6 (PCT/US2006/044853) dated May 11, 2009 (69 pages).
European Search Report from application No. EP 06838033.6 (PCT/US2006/044853) dated May 11, 2009 (7 pages).
European Search Report from corresponding European application No. 11165422.4 dated Aug. 8, 2011 (118 pages).
European Search Report from corresponding European application No. 11165423.2 dated Aug. 8, 2011 (118 pages).
European Search Report from European Application No. 10175751.6 dated Nov. 18, 2010 (8 pages).
European Search Report from European application No. 11165422.4 dated Aug. 8, 2011 (118 pages).
European Search Report from European application No. 11165423.2 dated Aug. 8, 2011 (118 pages).
European Search Report issued in European Application No. 08856764.9 dated Jun. 4, 2014 (3 pages).
Extended Search Report for EP10175727, 7 pages (dated Dec. 19, 2015).
Favale, A. et al., Pre-conceptual Design of a Rapid Cycling Medical Synchrotron, The AES/BNL collaboration, 45 pages (Oct. 27, 1999).
File History for U.S. Appl. No. 14/039,307 as of Jan. 13, 2017, 343 pages.
File history of U.S. Appl. No. 10/949,734 (now U.S. Pat. No. 7,208,748) (downloaded Mar. 14, 2017).
File History of U.S. Appl. No. 11/187,633.
File history of U.S. Appl. No. 11/187,633 (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 11/371,622 (now U.S. Pat. No. 7,402,963) (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 11/463,403 (now U.S. Pat. No. 7,656,258) (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 11/517,490 (now U.S. Pat. No. 7,701,677) (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 11/601,056 (now U.S. Pat. No. 7,728,311) (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 11/624,769 (now U.S. Pat. No. 7,541,905) (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 11/724,055 (now U.S. Pat. No. 7,718,982) (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 11/870,961 (now U.S. Pat. No. 8,003,964) (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 11/948,662 (now U.S. Pat. No. 8,581,523) (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 12/275,103 (now U.S. Pat. No. 8,344,340) (downloaded Mar. 14, 2017).
File History of U.S. Appl. No. 13/618,939.
File history of U.S. Appl. No. 14/039,307 (downloaded Mar. 13, 2017).
File history of U.S. Appl. No. 60/590,088 (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 60/850,565 (downloaded Mar. 14, 2017).
File history of U.S. Appl. No. 60/991,454 (downloaded Mar. 14, 2017).
File History of U.S. Pat. No. 7,402,963.
File History of U.S. Pat. No. 7,626,347.
File History of U.S. Pat. No. 8,952,634.
File History of U.S. Appl. No. 11/187,633, (Mar. 23, 2017).
First Office Action (Chinese translation) for CN201380062115.7, 7 pages (dated Dec. 12, 2016).
First Office Action (English translation) for CN201380062115.7, 9 pages (dated Dec. 12, 2016).
Fish & Richardson P.C., Response to Non Final Office action mailed Aug. 20, 2010 in U.S Appl. No. 11/948,359, filed Feb. 22, 2011 (17 pages).
Flanz et al., Large Medical Gantries, Particle Accelerator Conference, Massachusetts General Hospital, 1995, pp. 1-5.
Flanz et al., Operation of a Cyclotron Based Proton Therapy Facility, Massachusetts General Hospital, Boston, MA 02114, pp. 1-4, retrieved from Internet in 2009.
Flanz et al., The Northeast Proton Therapy Center at Massachusetts General Hospital, Fifth.Workshop on Heavy Charge Particles in Biology and Medicine, GSI, Darmstadt, Aug. 1995, 11 pages.
Flanz et al., Treating Patients with the NPTC Accelerator Based Proton Treatment Facility, Proceedings of the 2003 Particle Accelerator Conference, 2003, pp. 690-693.
Flanz, et al., “Scanning Beam Technologies”, PTCOG 2008, 28 pages.
Flood and Frazier, The Wide-Band Driven RF System for the Berkeley 88-Inch Cyclotron, American Institute of Physics, Conference Proceedings., No. 9, 1972, 459-466.
Foster and Kashikhin, Superconducting Superferric Dipole Magent with Cold Iron Core for the VLHC, IEEE Transactions on Applied Superconductivity, Mar. 2002, 12(1):111-115.
Friesel et al., Design and Construction Progress on the IUCF Midwest Proton Radiation Institute, Proceedings of EPAC 2002, 2002, pp. 2736-2738.
Fukumoto et al., A Proton Therapy Facility Plan Cyclotrons and their Applications, Proceedings of the 13th International Conference, Vancouver, Canada, Jul. 6-10, 1992, pp. 258-261.
Fukumoto, Cyclotron Versus Synchrotron for Proton Beam Therapy, KEK Prepr., No. 95-122, Oct. 1995, pp. 533-536.
Gordon, M.M. et. al., “Design Study for a Compact 200 MeV Cyclotron,” AIP Conference Proceedings Sixth International Cyclotron Conference, No. 9, pp. 78-86 (1972).
Gordon, M.M., “Extraction Studies for a 250 MeV Superconducting Synchrocyclotron,” Proceedings of the 1987 IEEE Particle Accelerator Conference: Accelerator Engineering and Technology, pp. 1255-1257 (1987).
Goto et al., Progress on the Sector Magnets for the Riken SRC, American Institute of Physics, 714 CP600, Cyclotrons and Their Applications 2001, Sixteenth International Conference, 2001, pp. 319-323.
Graffman et al., Acta Radial. Therapy Phys. Biol. 1970, 9, 1 (1970).
Graffman et al., Design Studies for a 200 MeV Proton Clinic for Radiotherapy, AIP Conference Proceedings: Cyclotrons—1972, 1972, No. 9, pp. 603-615.
Graffman, et. al. Proton radiotherapy with the Uppsala cyclotron. Experience and plans Strahlentherapie, 1985, 161(12):764-770.
Grözinger, Sven Oliver, Volume Conformal Irradiation of Moving Target vols. with Scanned Ion Beams, Vom Fachbereich Physik der Technischen Universitãt Darmstadt, 110 pages (2004).
Hede, Research Groups Promoting Proton Therapy Lite, Journal of the National Cancer Institute, Dec. 6, 2006, 98(23):1682-1684.
Heinz, Superconducting Pulsed Magnetic Systems for High-Energy Synchrotrons, Proceedings of the Fourth International Cryogenic Engineering Conference, May 24-26, 1972, pp. 55-63.
Hentschel et al., Plans for the German National Neutron Therapy Centre with a Hospital-Based 70 MeV Proton Cyclotron at University Hospital Essen/Germany, Cyclotrons and their Applications, Proceedings of the Fifteenth International Conference on Cyclotrons and their Applications, Caen, Franco, Jun. 14-19, 1998, pp. 21-23.
Hepburn et al., Superconducting Cyclotron Neutron Source for Therapy, International Journal of Radiation Oncology Biology Physics, vol. 3 complete, 1977, pp. 387-391.
Hirabayashi, Development of Superconducting Magnets for Beam Lines and Accelerator at KEK, IEEE Transaction on Magnetics, Jan. 1981, Mag-17(1 ):728-731.
Indiana's mega-million proton therapy cancer center welcomes its first patients [online] Press release, Health & Medicine Week, 2004, retrieved from NewsRx.com, Mar. 1, 2004, pp. 119-120.
International Preliminary Report on Patentability for PCT application No. PCT/US2007/001506 dated Jul. 5, 2007 (15 pages).
International Preliminary Report on Patentability from PCT application No. PCT/US2007/086109, dated Jun. 10, 2010 (6 pages).
International Preliminary Report on Patentability from PCT application No. PCT/US2008/084695, dated Jun. 10, 2010 (9 pages).
International Preliminary Report on Patentability from PCT application No. PCT/US2008/084699, dated Jun. 10, 2010 (6 pages).
International Preliminary Report on Patentability from PCT application No. PCT/US2013/062119 dated Mar. 31, 2015 (7 pages).
International Preliminary Report on Patentability from PCT application No. PCT/US2013/062137 dated Mar. 31, 2015 (9 pages).
International Search Report and Written Opinion for PCT application No. PCT/US2008/084695 dated Jan. 26, 2009 (9 pages).
International Search Report and Written Opinion from PCT application No. PCT/US2013/062119 dated Nov. 26, 2013 (9 pages).
International Search Report and Written Opinion in International Application No. PCT/US2008/084699, dated Feb. 4, 2009, 6 pages.
International Search Report dated Aug. 26, 2008 in PCT application No. PCT/US2007/086109 (3 pages).
International Search Report for PCT/US2007/001628 dated Feb. 18, 2008 (4 pages).
Ishibashi and Mcinturff, Stress Analysis of Superconducting 1 OT Magnets for Synchrotron, Proceedings of the Ninth International Cryogenic Engineering Conference, May 11-14, 1982, pp. 513-516.
Ishibashi and Mcinturff, Winding Design Study of Superconducting 10 T Dipoles for a Synchrotron, IEEE Transactions on Magnetics, May 1983, MAG-19(3):1364-1367.
Jahnke et al., First Superconducting Prototype Magnets for a Compact Synchrotron Radiation Source in Operation, IEEE Transactions on Magnetics, Mar. 1988, 24(2):1230-1232.
Japanese office action issued in Japanese application 2015-534728 dated Mar. 28, 2016 (6 pages). NOTE: English translation has not been received from Associate.
Jones and Dershem, Synchrotron Radiation from Proton in a 20 TEV, 10 TESLA Superconducting Super Collider Proceedings of the 12th International Conference on High-Energy Accelerator, Aug. 11-16, 1983, pp. 138-140.
Jones and Mills, The South African National Accelerator Centre: Particle Therapy and Isotope Production Programmes, Radiation Physics and Chemistry, Apr.-Jun. 1998, 51 ( 4-6):571-578.
Jones et al., Status Report of the NAC Particle Therapy Programme, Stralentherapie and Onkologie, vol. 175, Suppl. II, Jun. 1999, pp. 30-32.
Jones, Present Status and Future Trends of Heavy Particle Radiotherapy, Cyclotrons and their Applications 1998, Proceedings of the Fifteenth International Conference on Cyclotrons and their Applications, Jun. 14-19, 1998, pp. 13-20.
Jones, Progress with the 200 MeV Cyclotron Facility at the National Accelerator Centre, Commission of the European Communities Radiation Protection Proceedings, Fifth Symposium on Neutron Dosimetry, Sep. 17-21, 1984, vol. II, pp. 989-998.
Jongen et al., Development of a Low-cost Compact Cyclotron System for Proton Therapy, National Institute of Radio!. Sci, 1991, No. 81, DD. 189-200.
Jongen et al., Progress report on the IBA-SHI small cyclotron for cancer therapy Nuclear Instruments and Methods in Physics Research, Section B, vol. 79, issue 1-4, 1993, pp. 885-889.
Jongen et al., The proton therapy system for MGH's NPTC: equipment description and progress report, Bulletin du Cancer/Radiotherapie, Proceedings of the meeting of the European Heavy Particle Therapy Group, 1996, 83(Suppl. 1):219-222.
Jongen et al., The proton therapy system for the NPTC: Equipment Description and progress report, Nuclear Instruments and methods in physics research, 1996, Section B, 113(1 ): 522-525.
Kanai et al., Three-dimensional Beam Scanning for Proton Therapy, Nuclear Instruments and Methods in Physic Research, Sep. 1, 1983, The Netherlands, 214(23):491-496.
Kanazawa, M. et al., Beam Control in the Spot Scanning Irradiation, Proceedings of the Second Asian Particle Accelerator Conference, China; 846-848 (2001).
Karlin et al., Medical Radiology (Moscow), 1983, 28, 13.
Karlin et al., The State and Prospects in the Development of the Medical Proton Tract on the Synchrocyclotron in Gatchina, Med. Radial., Moscow, 28(3):28-32 (Mar. 1983)(German with English Abstract on end of p. 32).
Kats and Druzhinin, Comparison of Methods for Irradiation Prone Patients, Atomic Energy, Feb. 2003, 94(2): 120-123.
Kats and Onosovskii, A Planar Magnetooptical System for the Irradiation of a Lying Patient with a Proton Beam from Various Directions, Instruments and Experimental Techniques, 1996, 39(1):127-131.
Kats and Onosovskii, A Simple, Compact, Flat System for the Irradiation of a Lying Patient with a Proton Beam from Different Directions, Instruments and Experimental Techniques, 1996, 39(1):132-134.
Kawachi, K. et al., Three Dimensional Spot Beam Scanning Method for Proton Conformation Radiation Therapy, Acta Radiologica, Supplementum 364, 10 pages (1982).
Khoroshkov et al., Moscow Hospital-Based Proton Therapy Facility Design, Am. Journal Clinical Oncology: CCT, Apr. 1994, 17(2)1 09-114.
Kim and Blosser, Optimized Magnet for a 250 MeV Proton Radiotherapy Cyclotron, Cyclotrons and Their Applications 2001, May 2001, Sixteenth International Conference, pp. 345-347.
Kim and Yun, A Light-Ion Superconducting Cyclotron System for Multi-Disciplinary Users, Journal of the Korean Physical Society, Sep. 2003, 43(3):325-331.
Kim et al., Construction of 8T Magnet Test Stand for Cyclotron Studies, IEEE Transactions on Applied Superconductivity, Mar. 1993, 3(1):266-268.
Kim et al., Design Study of a Superconducting Cyclotron for Heavy Ion Therapy, Cyclotrons and Their Applications 2001, Sixteenth International Conference, May 13-17 2001, pp. 324-326.
Kim et al., Trim Coil System for the Riken Cyclotron Ring Cyclotron, Proceedings of the 1997 Particle Accelerator Conference, IEEE, Dec. 1981, vol. 3, pp. 214-235 OR 3422-3424, 1998.
Kim, An Eight Tesla Superconducting Magnet for Cyclotron Studies, Ph.D. Dissertation, Michigan State University, Department of Physics and Astronomy, 1994, 13 8 pages.
Kimstrand, Beam Modelling for Treatment Planning of Scanned Proton Beams, Digital Comprehensive Summaries of Uppsala dissertations from the Faculty of Medicine 330, Uppsala Universitet, 2008, 58 pages.
Kishida and Yano, Beam Transport System for the RIKEN SSC (II), Scientific Papers of the Institute of Physical and Chemical Research, Dec. 1981, 75(4):214-235.
Koehler et al., Range Modulators for Protons and Heavy Ions, Nuclear Instruments and Methods, 1975, vol. 131, pp. 437-440.
Koto and Tsujii, Future of Particle Thera12y, Ja12anese Journal of Cancer Clinics, 2001, 47(1):95-98 [Lang.: Japanese], English abstract (htt12://sciencelinks.j12/jeast/article/200206/000020020601A05 I I 453 .nhn).
Kraft et al., Hadrontherapy in Oncology, U. Amaldi and Larrsson, editors Elsevier Science, 1994, 161 pages.
Krevet et al., Design of a Strongly Curved Superconducting Bending Magnet for a Compact Synchrotron Light Source, Advances in Cryogenic Engineering, 1988, vol. 33, pp. 25-32.
Laisne et al., the Orsay 200 MeV Synchrocyclotron, IEEE Transactions on Nuclear Science, Apr. 1979, NS-26(2):1919-1922.
Larsson et al., Nature, 1958, 182:1222.
Larsson, Biomedical Program for the Converted 200-MeV Synchrocyclotron at the Gustaf Werner Institute, Radiation Research, 1985, 104:S310-S318.
Lawrence et al., Heavy particles in acromegaly and Cushing's Disease, in Endocrine and Norendocrine Hormone Producing Tumors (Year Book Medical Chicago, 1973, pp. 29-61.
Lawrence et al., Successful Treatment of Acromegaly: Metabolic and Clinical Studies in 145 Patients, The Journal of Clinical Endrocrinology and Metabolism, Aug. 1970, 31(2), 21 pages.
Lawrence et al., Treatment of Pituitary Tumors, (Excerpta medica, Amsterdam/American Elsevier, New York, 1973, pp. 253-262.
Lawrence, Cancer, 1957, 10:795.
Lecroy et al., Viewing Probe for High Voltage Pulses, Review of Scientific Instruments USA, Dec. 1960, 31(12):1354.
Lin et al., Principles and 10 Year Experience of the Beam Monitor System at the PSI Scanned Proton Therapy Facility, Center for Proton Radiation Therapy, Paul Scherrer Institute, CH-5232, Villigen PSI, Switzerland, 2007, 21 pages.
Linfoot et al., Acromegaly, in Hormonal Proteins and Peptides, edited by C.H. Li, 1975, pp. 191-246.
Literature Author and Keyword Search, Feb. 14, 2005, 44 pages.
Literature Keyword Search, Jan. 24, 2005, 98 pages.
Literature Search and Keyword Search for Synchrocyclotron, Jan. 25, 2005, 68 pages.
Literature Search by Company Name/Component Source, Jan. 24, 2005, 111 pages.
Literature Search, Jan. 26, 2005, 37 pages.
Livingston et al., A capillary ion source for the cyclotron, Review Science Instruments, Feb. 1939, 10:63.
LLNL, UC Davis Team Up to Fight Cancer, Lawrence Livermore National Laboratory, Apr. 28, 2006, SF-06-04-02, Livermore, California, pp. 1-4.
Lorin, S. et al., Development of a compact proton scanning system in Uppsala with a moveable second magnet, Phys. Med. Biol, 45:1151-1163 (2000).
Mandrillon, High Energy Medical Accelerators, EPAC 90, 2nd European Particle Accelerator Conference, Jun. 12-16, 1990, 2:54-58.
Marchand et al., IBA Proton Pencil Beam Scanning: an Innovative Solution for Cancer Treatment, Proceedings of EP AC 2000, Vienna, Austria, 3 pages.
Marti et al., High Intensity Operation of a Superconducting Cyclotron, Proceedings of the I 4the International Conference, Cyclotrons and Their Applications, Oct. 1995, pp. 45-48 (Oct. 1995).
Martin, Operational Experience with Superconducting Synchrotron Magnets Proceedings of the 1987 IEEE Particle Accelerator Conference, Mar. 16-19, 1987, vol. 3 of 3: 1379-1382.
Meote et al., ETOILE Hadrontherapy Project, Review of Design Studies Proceedings of EPAC 2002, 2002, pp. 2745-2747.
Miyamoto et al., Development of the Proton Therapy System, The Hitachi Hyoron, 79(10):775-775 779 (1997) [Lang: Japanese], English abstract (http://www.hitachi.com/rev/1998/revfeb98/rev4 706.htm).
Montelius et al., The Narrow Proton Beam Therapy Unit at the Svedberg Laboratory in Uppsala, ACTA Oncologica, 1991, 30:739-745.
Moser et al., Nonlinear Beam Optics with Real Fields in Compact Storage Rings, Nuclear Instruments & Methods in Physics Research/Section B, B30, Feb. 1988, No. 1, pp. 105-109.
Moyers et al., A Continuously Variable Thickness Scatterer for Proton Beams Using Self-compensating Dual Linear Wedges Loma Linda University Medical Center, Dept. of Radiation Medicine, Loma Linda, CA, Nov. 2, 1992, 21 pages.
Murphy, M. and Lin, P., Intra-fraction dose delivery timing during stereotactic radiotherapy can influence the radiobiological effect, Med. Phys., 34(2):481-484 (2007).
National Cancer Institute Funding (Senate-Se12tember 21, I 992} (w>lvw.tbomas.loc.gov/cgibin/querv/z?r102:321SE2-712 12 na2es).
Nicholson, Applications of Proton Beam Therapy, Journal of the American Society of Radiologic Technologists, May/Jun. 1996, 67(5): 439-441.
Nolen et al., The Integrated Cryogenic—Superconducting Beam Transport System Planned for MSU, Proceedings of the J21h International Conference on High-Energy Accelerators, Aug. 1983, pp. 549-551.
Non Final Office Action from U.S. Appl. No. 12/275,103 dated Feb. 1, 2011 (6 pages).
Non Final Office Action from U.S. Appl. No. 12/618,297 dated May 13, 2011 (44 pages).
Non Final Office Action from U.S. Appl. No. 12/618,297 dated May 13, 2011 (57 pages).
Norimine et al., A Design of a Rotating Gantry with Easy Steering for Proton Therapy, Proceedings of EPAC 2002, 2002, pp. 2751-2753.
Office Action and response history of U.S. Appl. No. 11/601,056 dated Aug. 24, 2009.
Office Action and response history of U.S. Appl. No. 11/601,056 dated Mar. 24, 2009.
Office Action and response history of U.S. Appl. No. 11/601,056 dated Jan. 14, 2010.
Office Action for JP2015-534721, 14 pages (dated Feb. 3, 2016) (in both Japanese and English).
Office action from Canadian Application No. 2,574,122 dated Nov. 14, 2012 (6 pages).
Office action from U.S. Appl. No. 11/948,662, dated Oct. 14, 2011 (5 pages).
Office Action with English translation from Japanese Application No. 2007-522777 dated Oct. 4, 2011 (15 pages).
Office action with English translation from Taiwanese application No. 097144546 dated Oct. 25, 2013 (27 pages).
Office action with English Translation issued in Chinese Application No. 201010581384.2 dated Nov. 10, 2011 (19 pages).
Ogino, Takashi, Heavy Charged Particle Radiotherapy-Proton Beam, Division of Radiation Oncology, National Cancer Hospital East, Kashiwa, Japan, Dec. 2003, 7 pages.
Okumura et al., Overview and Future Prospect of Proton Radiotherapy, Japanese Journal of Cancer Clinics, 1997, 43(2):209-214 [Lang.: Japanese].
Okumura et al., Proton Radiotherapy Japanese Journal of Cancer and Chemotherapy, 1993, 10. 20(14):2149-2155[Lang.: Japanese].
Ormrod, J.H., et al., The Chalk-River Superconducting Cyclotron, Proceedings of the International Conference on Cyclotrons and their applications '79, 1979 (6 pages).
Outstanding from Search Reports, Accelerator of Polarized Portons at Fermilab, 2005, 20 pages.
Paganetti et al., Proton Beam Radiotherapy—The State of the Art, Springer Verlag, Heidelberg, ISBN 3-540-00321-5, Oct. 2005, 36 pages.
Palmer and Tollestrup, Superconducting Magnet Technology for Accelerators, Annual Review of Nuclear and Particle Science, 1984, vol. 34, pp. 247-284.
Pardo, J. et al., Simulation of the performance of the CNAO facility's Beam Delivery System, PTCOG 46, Zibo, China, 17 pages (2007).
Patent Assignee and Keyword Searches for Synchrocyclotron, Jan. 25, 2005, 78 pages.
Patent Assignee Search ‘Paul Scherrer Institute, Library Services at Fish & Richardson P.C., Mar. 20, 2007, 40 pages.
Patent Prior Art Search for ‘Proton Therapy System’, Library Services at Fish & Richardson P.C., Mar. 20, 2007, 46 pages.
Pavlovic, Beam-optics study of the gantry beam delivery system for light-ion cancer therapy, Nuclear Instruments and Methods in Physics Research, Section A, Nov. 1997, 399(2):439-454(16).
PCT International Preliminary Report on Patentability of corresponding PCT application No. PCT/US2006/044853, dated May 20, 2008 (7 pages).
PCT International Search report and Written Opinion of PCT application No. PCT/US2006/044853, dated Oct. 5, 2007 (7 pages).
Pedroni and Enge, Beam optics design of compact gantry for proton therapy Medical & Biological Engineering & Computing, May 1995, 33(3):271-277.
Pedroni and Jermann, SGSMP: Bulletin Mar. 2002 Proscan Project, Progress Report on the PROSCAN.
Pedroni et al., A Novel Gantry for Proton Therapy at the Paul Scherrer Institute, Cycloctrons and Their Applications 2001: Sixteenth International Conference. AIP Conference Proceedings, 2001, 600:13-17.
Pedroni et al., The 200-MeV proton therapy project at the Paul Scherrer Institute: Conceptual design and practical realization, Medical Physics, Jan. 1995, 22(1 ):37-53.
Pedroni, Accelerators for Charged Particle Therapy: Performance Criteria from the User Point of View, Cyclotrons and their Applications, Proceedings of the 13th International Conference, Jul. 6-10, 1992, pp. 226-233.
Pedroni, E. et al., Cancer Therapy with 200 MEV Protons at PSI. Development of a Fast Beam Scanning Method and Future Plans for a Hospital Based Facility, pp. 277-279 (1990).
Pedroni, Latest Developments in Proton Therapy Proceedings of EPAC 2000, pp. 240-244, 2000.
Pedroni, Status of Proton Therapy: results and future trends, Paul Scherrer Institute, Division of Radiation Medicine, 1994, 5 pages.
Peggs et al., A Survey of Hadron Therapy Accelerator Technologies, Particle Accelerator Conference, Jun. 25-29 2008, 7 pages.
Potts et al., MPWP6-Therapy III: Treatment Aids and Techniques Medical Physics, Sep./Oct. 1988, 15(5):798.
Pourrahimi et al., Powder Metallurgy Processed Nb3Sn(Ta) Wire for High Field NMR magnets, IEEE Transactions on Applied Superconductivity, Jun. 1995, 5(2):1603-1606.
Prieels et al., The IBA State-of-the-Art Proton Therapy System, Performances and Recent Results, Application of Accelerators in Research and industry—Sixteenth Int'l Conj, American Institute of Physics, Nov. 1-5, 2000, 576:857-860.
Program Chart (Oct. 7, 2006-Oct. 11, 2016), 8 pages.
Rabin et al., Compact Designs for Comprehensive Proton Beam Clinical Facilities, Nuclear Instruments & Methods in Physics Research, Apr. 1989, Section B, vol. 40-41, Part II, pp. 1335-1339.
Rainwater, James, Status of the Nevis Synchrocyclotron Modification, AIP Conference Proceedings No. 9, 1972 (14 pages).
Renner et al., “Preliminary Results of a Raster Scanning Beam Delivery System”, IEEE, 1989, 3 pages.
Research & Development Magazine, Proton Therapy Center Nearing Completion, Aug. 1999, 41(9):2 pages (www.rdmag.com).
Resmini Design Characteristics of the K=800 Superconducting Cyclotron at M.S.U., Cyclotron Laboratory, Michigan State University, East Lansing, Michigan 48824, IEEE Transaction on Nuclear Science, vol. NS-26, No. 2, Apr. 1979, 8 pages.
Response to Chinese Office action dated Jan. 25, 2010 in Chinese application No. 200680051421.0, filed Jun. 24, 2010 (34 pages).
Response to European Communication issued in European application No. 13774886.9 dated Jun. 12, 2015, filed on Dec. 9, 2015 (26 pages).
Response to European Communication issued in European application No. 13783422.2 dated Jun. 12, 2015, filed on Dec. 8, 2015 (19 pages).
Response to European Communication dated Jun. 12, 2015 in European application No. 13774886.9 filed on Dec. 6, 2015 (26 pages).
Response to European Communication dated Apr. 20, 2010, from European application No. 06838033.6, filed Nov. 2, 2010 (13 pages).
Response to examination search report filed in European Application No. 05776532.3 dated Dec. 20, 2011 (14 pages).
Response to Non Final Office Action dated Feb. 1, 2011 in U.S. Appl. No. 12/275,103, filed May 2, 2011 (13 pages).
Response with English translation to Chinese Office action filed in Chinese Application No. 200880125832.9 dated Dec. 16, 2013 (12 pages).
Response with English translation to Chinese Office Action from Chinese application No. 200880125832.9 dated Sep. 22, 2011, filed on Apr. 9, 2012 (23 pages).
Response with English translation to Japanese Office action filed Mar. 1, 2012 in Japanese Application No. 2007-522777 (14 pages).
Response with English translation to office action dated Oct. 25, 2013 in Taiwanese Application No. 097144546, filed on Mar. 28, 2014 (34 pages).
RetroSearch Berkeley 88-Inch Cyclotron ‘RF’ or ‘Frequency Control’, Jan. 21, 2005, 36 pages.
RetroSearch Berkeley 88-Inch Cyclotron, Jan. 24, 2005, 170 pages.
RetroSearch Bernard Gottschalk, Cyclotron, Beams, Compensated Upstream Modulator, Compensated Scatter, Jan. 21, 2005, 20 pages.
RetroSearch Cyclotron with ‘RF’ or ‘Frequency Control’, Jan. 21, 2005, 49 pages.
RetroSearch Gottschalk, Bernard, Harvard Cyclotron Wheel, Jan. 21, 2005, 20 pages.
RetroSearch Loma Linda University Beam Compensation, Jan. 21, 2005, 60 pages.
RetroSearch Loma Linda University, Beam Compensation Foil Wedge, Jan. 21, 2005, 15 pages.
Revised Patent Keyword Search, Jan. 25, 2005, 86 pages.
Rifuggiato et, al., Status Report of the LNS Superconducting Cyclotron Nukleonika, 2003, 48:SI31-SI34, Supplement 2.
Rode, Tevatron Cryogenic System, Proceedings of the 12th International Conference on Highenergy Accelerators, Fermilab, Aug. 11-16, 1983, pp. 529-535.
Salzburger et al., Superconducting Synchrotron Magnets Supraleitende Synchrotronmagnete, NTiS, 155 pages (Oct. 1975).
Schillo et al,. Compact Superconducting 250 MeV Proton Cyclotron for the PSI Proscan Proton Therapy Project, Cyclotrons and Their Applications 2001, Sixteenth International Conference, 2001, pp. 37-39.
Schneider et al., Nevis Synchrocyclotron Conversion Program—RF System, IEEE Transactions on Nuclear Science USA, Jun. 1969, ns 16(3): 430-433.
Schneider et al., Superconducting Cyclotrons, IEEE Transactions on Magnetics, vol. MAG-11, No. 2, Mar. 1975, New York, pp. 443-446.
Schreuder et al., The Non-orthogonal Fixed Beam Arrangement for the Second Proton Therapy Facility at the National Accelerator Centre, Application of Accelerators in Research and Industry, American Institute of Physics, Proceedings of the Fifteenth International Conference, Nov. 1998, Part Two, pp. 963-966.
Schreuder, Recent Developments in Superconducting Cyclotrons, Proceedings of the 1995 Particle Accelerator Conference, May 1-5, 1995, vol. 1, pp. 317-321.
Schubert and Blosser, Conceptual Design of a High Field Ultra-Compact Cyclotron for Nuclear Physics Research, Proceedings of the 1997 Particle Accelerator Conference, May 12-16, 1997, vol. 1, 3 pp. 1060-1062.
Schubert, Extending the Feasibility Boundary of the Isochronous Cyclotron, Dissertation submitted to Michigan State University, 1997, Abstract http://adsabs.harvard.edu/abs/1998PhDt . . . 147S.
Shelaev et al., Design Features of a Model Superconducting Synchrotron of JINR, Proceedings of the 12th International Conference on High-energy Accelerators, Aug. 11-16, 1983, pp. 416-418.
Shinji Sato et al., “Dynamic Intensity Control System with RF-knockout Slow-Extraction in the HIMAC Synchrotron-” Nuclear Instruments and Methods in Physics Research A 574, 2007, pp. 226-231.
Shintomi et. Al, Technology and Materials for the Superconducting Super Collider (SSC) Project, [Lang.: Japanese], The Iron and Steel Institute of Japan 00211575, 78(8): 1305-1313, 1992, http://ci.nii.ac.ip/naid/I I 0001493249/en/.
Single Room Proton Therapy Facility, ACCEL, Oct. 2006, 1 page.
Sisterson, Clinical use of proton and ion beams from a world-wide perspective, Nuclear Instruments and Methods in Physics Research, Section B, 1989, 40-41:1350-1353.
Sisterson, World Wide Proton Therapy Experience in 1997, The American Insitute of Physics, Applications of Accelerators in Research and Industry, Proceedings of the Fifteenth International Conference, Part Two, Nov. 1998, pp. 959-962.
Slater et al., Developing a Clinical Proton Accelerator Facility: Consortium-Assisted Technology Transfer, Conference Record of the 1991 IEEE Particle Accelerator Conference: Accelerator Science and Technology, vol. I, May 6-9, 1991, pp. 532-536.
Slater et al., Development of a Hospital-Based Proton Beam Treatment Center, International Journal of Radiation Oncology J Biology J Physics, Apr. 1988, 14(4):761-775.
Smith et al., The Northeast Proton Therapy Center at Massachusetts General Hospital Journal of Brachytherapy International, Jan. 1997, pp. 137-139.
Snyder and Marti, Central region design studies for a proposed 250 MeV proton cyclotron, Nuclear Instruments and Methods in Physics Research, Section A, 1995, vol. 355, pp. 618-623.
Soga, Progress of Particle Therapy in Japan, Application of Accelerators in Research and Industry, American Institute of Physics, Sixteenth International Conference, Nov. 2000, pp. 869-872.
Source Search “Cites of U.S. and Foreign Patents/Published applications in the name of Mitsubishi Denki Kabushiki Kaisha and Containing the Keywords (Proton and Synchrocyclotron),” Jan. 2005, 8 pages.
Spiller et al., The GSI Synchrotron Facility Proposal for Acceleration of High Intensity Ion and Proton Beams Proceedings of the 2003 Particle Accelerator Conference, May 12-16, 2003, vol. 1, pp. 589-591.
Stanford et al., Method of Temperature Control in Microwave Ferroelectric Measurements, Sperry Microwave Electronics Company, Clearwater, Florida, Sep. 19, 1960, 1 page.
Superconducting Cyclotron Contract awarded by Paul Scherrer Institute (PSI), Villigen, Switzerland, http://www.accel.de/News/superconducting—cyclotron—contract.htm, Jan. 2009, 1 page.
Tadashi et al., Large superconducting super collider (SSC) in the planning and materials technology, 78(8):1305-1313, The Iron and Steel Institute of Japan 00211575, Aug. 1992.
Takada, Conceptual Design of a Proton Rotating Gantry for Cancer Therapy, Japanese Journal of Medical Physics, 1995, 15(4):270-284.
Takada, Y. “A Review of Rotating Gantries for Heavy Charged Particle Therapy,” Symposium of Research Center for Charged Particle Therapy on Fundamental Development of the Charged Particle Therapy, Chiba (Japan), Nov. 13-14, 2001.
Takayama et al., Compact Cyclotron for Proton Therapy, Proceedings of the 81h Symposium on Accelerator Science and Technology, Japan, Nov. 25-27, 1991, pp. 380-382.
Teng, The Fermilab Tevatron, Coral Gables 1981, Proceedings, Gauge Theories, Massive Neutrinos, and Proton Decay, 1981, pp. 43-62.
The Davis 76-Inch Isochronous Cyclotron, Beam On: Crocker Nuclear Laboratory, University of California, 2009, 1 page.
The Journal of Practical Pharmacy, 1995, 46(1):97-103 [Japanese].
The K100 Neutron-therapy Cyclotron, National Superconducting Cyclotron Laboratory at Michigan State University (NSCL ), retrieved from: http://www.nscl.msu.edu/tech/accelerators/kl 00, Feb. 2005, 1 page.
The K250 Proton therapy Cyclotron, National Superconducting Cyclotron Laboratory at Michigan State University (NSCL), retrieved from: http://www.nscl.msu.edu/tech/accelerators/k.250.html, Feb. 2005, 2 pages.
The K250 Proton-therapy Cyclotron Photo Illustration, National Superconducting Cyclotron Laboratory at Michigan State University (NSCL), retrieved from: http://www.nscl.msu.edu/media/image/ experimental-equipment-technology /25 0 .html, Feb. 2005, 1 page.
Timmer, “The ACCEL Single Room Proton Therapy Facility” ACCEL Instruments GmbH, PTCOG 45, Oct. 2006, Houston, Texas, 18 pages.
Tobias et al., Cancer Research, 1958, 18, 121 (1958).
Tom, The Use of Compact Cyclotrons for Producing Fast Neutrons for Therapy in a Rotatable Isocentric Gantry, IEEE Transaction on Nuclear Science, Apr. 1979, 26(2):2294-2298.
Toyoda, Proton Therapy System, Sumitomo Heavy Industries, Ltd., 2000, 5 pages.
Trinks et. al., The Tritron: A Superconducting Separated-Orbit Cyclotron, Nuclear Instruments and Methods in Physics Research, Section A, 1986, vol. 244, pp. 273-282.
Tsuji, H., “Cancer Therapy Using Proton Beams: the Newest State of Affairs and Future Prospects,” Isotope News, No. 9, pp. 2-7 (1992). (English Abstract).
Tsuji, The Future and Progress of Proton Beam Radiotherapy, Journal of Japanese Society for Therapeutic Radiology and Oncology, 1994, 6(2):63-76.
U.S. Appl. No. 11/870,961, filed Oct. 11, 2007, including application as filed (including pending claims).
U.S. Examiner Ephrem Alemu, U.S. Non Final Office Action in U.S. Appl. No. 11/948,359, dated Aug. 20, 2010 (12 pages).
U.S. Appl. No. 13/830,792, filed Mar. 14, 2013, including the USPTO electronic file for U.S. Appl. No. 13/830,792.
U.S. Appl. No. 13/949,459. filed Jul. 24, 2013, including the USPTO electronic file for U.S. Appl. No. 13/949,459.
U.S. Appl. No. 60/590,088, filed Jul. 21, 2004, including application as filed.
U.S. Appl. No. 60/738,404, filed Nov. 18, 2005, including application as filed.
U.S. Appl. No. 60/991,454, filed Nov. 30, 2007, including application as filed.
U.S. Appl. No. 61/676,377, filed Jul. 27, 2012, including the USPTO electronic file for U.S. Appl. No. 61/676,377.
UC Davis “Crocker Nuclear Laboratory Houses a Medium-Energy Particle Accelerator,” Crocker Nuclear Laboratory, University of California (2009).
UC Davis School of Medicine, Unlikely Partners Tum Military Defense into Cancer Offense, Current Issue Summer 2008, Sacramento, California, pp. 1-2.
Uli Weber et al., “Depth Scanning For A Conformal Ion Beam Treatment Of Deep Seated Tumours-” Physics in Medicine and Biology IOP Publishing UK, vol. 45, No. 12, Dec. 2000, pp. 3627-3641.
Umegaki et al., Development of an Advanced Proton Beam Therapy System for Cancer Treatment Hitachi Hyoron, 2003, 85(9):605-608 [Lang.: Japanese], English abstract, http://www.hitachi.com/ICSFiles/afieldfile/2004/06/0 l/r2003—04—l 04.pdf or http://www.hitachi.com/rev/archive/2003/2005649—12606.html (full text) [Hitachi, 52( 4), Dec. 2003].
Umezawa et al., Beam Commissioning of the new Proton Therapy System for University of Tsukuba, Proceedings of the 2001 Particle Accelerator Conference, vol. 1, Jun. 18-22, 2001, pp. 648-650.
van Steenbergen, Superconducting Synchroton Development at BNL, Proceedings of the 8th International Conference on Hi£h-Ener5'Y Accelerators CERN 1971, 1971, pp. 196-198.
van Steenbergen, The CMS, a Cold Magnet Synchrotron to Upgrade the Proton Energy Range of the BNL Facility, IEEE Transactions on Nuclear Science, Jun. 1971, 18(3):694-698.
Vandeplassche et al., 235 MeV Cyclotron for MGH's Northeast Proton Therapy Center (NPTC): Present Status, EPAC 96, Fifth European Partical Accelerator Conference, vol. 3, Jun. 10-14, 1996, pp. 2650-2652.
Verster, N.F.,: Regenerative Beam Extraction from the 150-MeV Synchrocyclotron at the Laboratoire Curie, Proceedings of Sector-Focused Cyclotrons 1959, 1959, pp. 224-229 (6 pages).
Voluntary amendment filed Apr. 18, 2011 in corresponding Chinese application No. CN200780102281.X, including English translation of claim amendments (10 pages).
Voluntary amendment filed in Canadian Application No. 2,574,122 dated Jul. 26, 2010 (16 pages).
Voluntary amendment filed in Canadian Application No. 2,574,122 dated Nov. 5, 2010 (15 pages).
Voluntary amendment filed in Canadian Application No. 2707075 dated Oct. 13, 2013 (8 pages).
Voluntary Amendment filed in Canadian Application No. 2707075 dated Oct. 18, 2013 (8 pages).
Vorobiev et al., Concepts of a Compact Achromatic Proton Gantry with a Wide Scanning Field, Nuclear Instruments and Methods in Physics Research, Section A., 1998, 406(2):307-310.
Vrenken et al., A Design of a Compact Gantry for Proton Therapy with 2D-Scanning, Nuclear Instruments and Methods in Physics Research, Section A, 1999, 426(2):618-624.
Wikipedia, Synchrotron http://en.wiki11edia.org/wiki/Synchrotron (originally visited Oct. 6, 2005, revisited Jan. 28, 2009), 7 pages.
Worldwide Patent Assignee Search, Jan. 24, 2005, 224 pages.
Worldwide Patent Keyword Search, Jan. 24, 2005, 94 pages.
Written Opinion dated Aug. 26, 2008 in PCT application No. PCT/US2007/086109 (5 pages).
Written Opinion for PCT/US2007/001628, dated Feb. 18, 2008 (11 pages).
Wu, Conceptual Design and Orbit Dynamics in a 250 MeV Superconducting Synchrocyclotron, Ph.D. Dissertation, Michigan State University, Department of Physics and Astronomy, 1990, 172 pages.
York et al., Present Status and Future Possibilities at NSCL-MSU, EP AC 94, Fourth European Particle Accelerator Conference, pp. 554-556, Jun. 1994.
York et al., The NSCL Coupled Cyclotron Project—Overview and Status, Proceedings of the Fifteenth International Conference on Cyclotrons and their Applications, Jun. 1998, pp. 687-691.
Yudelev et al., Hospital Based Superconducting Cyclotron for Neutron Therapy: Medical Physics Perspective, Cyclotrons and their applications 2001, 16th International Conference. American Institute of Physics Conference Proceedings, vol. 600, May 13-17, 2001, pp. 40-43.
Zherbin et al., Proton Beam Therapy at the Leningrad Synchrocyclotron (Clinicomethodological Aspects and Therapeutic Results), Aug. 1987, 32(8):17-22, (German with English abstract on pp. 21-22).
Angert, N (GSI, Darmstadt), CAS—CERN Accelerator School : 5th General Accelerator Physics Course, Jyväskylä , Finland, Sep. 7-18, 1992, pp. 619-642 (CERN-1994-001).
Second Office Action (Chinese translation) for CN201380062111.9, 10 pages (dated Apr. 5, 2017).
Second Office Action (English translation) for CN201380062111.9, 16 pages (dated Apr. 5, 2017).
Related Publications (1)
Number Date Country
20140094638 A1 Apr 2014 US
Provisional Applications (1)
Number Date Country
61707466 Sep 2012 US