The subject invention pertains to a method and apparatus for MR-guided biopsy. The subject invention can be applied to prostate biopsy. In a specific embodiment, the subject invention relates to a stereotactic positioning device for MR-guided interventions, such as biopsies of suspicious areas of the prostate gland. MRI (magnetic resonance imaging) is a current radiological imaging modality to view soft tissue lesions of the human body. MR can be used to guide the subject positioning device to directly puncture lesions in the prostate and/or to biopsy these.
Prostate cancer is the most common cancer, excluding skin cancers, in American men. The American Cancer Society estimates that during 2002 about 189,000 new cases of prostate cancer will be diagnosed in the United States. Accurate determination of the extent of local disease in the prostate is difficult. Current imaging techniques include, for example, transrectal ultrasound (TRUS), endorectal coil magnetic resonance imaging (MRI), and proton magnetic resonance spectroscopic imaging (MRSI). The reported accuracy of TRUS for determining if prostate cancer is confined within the capsule varies widely from 58% to 90%. However, preliminary data from recent studies of endorectal MRI show higher accuracy (75-90%) than TRUS, and better consistency.
In addition to morphologic extent, directed biopsy and assessment of tumor aggressiveness are important for accurate staging and treatment for prostate cancer when there is an elevated PSA. Current biopsy techniques are based on random spatial sampling and have a lower than desired sensitivity (60-70%) for identification of carcinoma of the prostate. Early preliminary studies of combined MRI/MRSI demonstrated localization of cancer to a sextant of the prostate with sensitivity up to 95% and specificity up to 91%. However, more specifically localized biopsies, rather than randomly taken biopsies, would be desirable.
MRI is presently regarded as the best imaging modality for assessing soft-tissue tumors like prostate cancer. This is confirmed by numerous reports in the literature. In an early study, carried out from December 1987 to April 1989, Rifkin et al [7] report on the collaborative effort of five institutions that are part of the Radiological Diagnostic Oncology Group. More than 200 patients who were thought clinically to have localized cancer of the prostate were studied preoperatively with both MRI and transrectal ultrasonography to evaluate the ability of these techniques to determine the exterit (stage) of the tumor. They underwent radical prostatectomy, and radiologic and pathological findings were correlated. The overall staging accuracy of ultrasonography was 58% (126 of 219 patients), with a standard error of 3%. The overall staging accuracy of MRI was 69% (133 of 194 patients), with a standard error of 3%. The subject invention can increase the diagnostic accuracy of MRI when combining MRI scans with interventional biopsy techniques.
Prostate cancer is the second most common cause of cancer death in US men. Its incidence is on the rise because more cancers are detected due to wide-ranging screening programs using either digital rectal exams or serum prostate-specific antigen (PSA). Whenever abnormalities crop up in these examinations, the patient is traditionally referred for ultrasound-guided biopsy, which has a low sensitivity and a specificity of only 60% for cancer detection [3]. This is why ultrasound is often used just to guide biopsies. However, MRI performs much better at cancer detection.
Typical prostate biopsies are performed by palpation (whether or not a nodule is present) or using ultrasound guidance (when a visible lesion is present). However, endorectal ultrasound is not sensitive enough for a screening tool. The visibility of the anterior capsule is poor as is visualization of seminal vesicle and lymph node involvement. Extracapsular disease and lymph node involvement is better picked up with MR, although interobserver variability is quite high (positive predictive value ˜70%). PSA and proton MR spectroscopy get higher ratings for predicting the Gleason grade. Patients with incompatible PSA and biopsy results or MR spectroscopy results or with MR visible lesions would thus benefit from an MR guided prostate biopsy.
The subject invention pertains to a method and apparatus for MR-guided biopsy. The subject invention can be applied to, for example, prostate biopsy. In a specific embodiment, the subject invention can provide a mechanical tool for stabilizing the patient in prone position and to guide a biopsy needle into defined targeted lesions in the prostate gland. The patient can lay prone in the MRI. The subject apparatus can guide an MR-visible, sterile needle sleeve, which can have a hollow tube filled with contrast media, through the anus onto the inner wall of the colon. Due to the visibility of the contrast media in the sleeve, the apparatus can be guided to the exact position. The sleeve can incorporate a tube within the contrast media filled sleeve to insert the biopsy needle and to push this needle forward into the prostate. The subject apparatus can utilize various mechanical means to stereotactically move the needle or needle sleeve in various directions.
Numbers used to describe the features in the drawings:
1 patient
2 biopsy needle
3 anus
4 positioning cushion
5 prostate
6 holding arm
7 axis
8 needle holder
9 stick
10 grip
11 tool to attach to parts of the prostate biopsy system
13 positioning cushion
14 base plate
15 arm-mounting-track
16 lower arm
17 upper arm
18 arm mounting lock-bolt
19 adjustment screw
20 sliding-part of the lower arm 16
21 base-part of the lower arm 16
22 needle-sleeve holder
23 lock-bolt
24 needle-sleeve
25 needle-sleeve-block
26 needle-sleeve-lock-in mechanism
27 outer tube
28 inner tube
29 seal stop
30 hollow space
31 snap-on mechanism
32 positioning system
33 patient
34 ball-and-socket-joint
35 curved inner needle
36 outer straight needle
37 grip of 36
38 grip of 35
40 ureter
41 mechanical axial fixation
42 locking mechanism
43 locking lever
45 coaxial hub tube
46 sliding stopper
47 needle plate
48 biopsy device
49 lock mechanism
50 operating screw
51 needle-sleeve
52 needle-sleeve-block
53 base plate
54 lower arm
55 upper arm
The subject invention pertains to a method and apparatus for MR-guided biopsy. In a specific embodiment, the subject invention can be utilized for prostate biopsy. In a specific embodiment, the subject invention relates to a positioning device for prostate interventions, which can incorporate many parts, such as a biopsy needle, a needle sleeve, various positioning and adjustment parts, coils, and more.
There are two ways to operate this embodiment, and later described prostate biopsy embodiments, in conjunction with magnetic resonance imaging (MRI). In a first technique the patient is pulled out from the MR magnet to operate the device, pushed back in the magnet to control the position of the needle guide, and pulled out from the magnet for further needle adjustments if needed. The dimensions for the necessary corrections can be taken from the image and transferred to the scales of the device. In a second technique, the patient stays in the magnet and images are taken during the needle repositioning procedure. The device will appear in the image and is operated from the outside by simply reaching in with the arm of the operator or by remotely operated tools. These tools can be, for example, long plastic sticks 9. Sticks 9 can be between 50 cm and 150 cm long, and 5 mm to 20 mm in diameter. Sticks 9 can have a grip 10 on the proximal end and a tool 11 at the distal end to attach to a particular part of the prostate biopsy device. The attachment tool 11 can, for instance, attach directly to the grip of the biopsy needle 2 for the purpose of adjusting the position and pushing the needle 2 into the tissue. The attachment tool 11 can be changed to attach to different parts. The stick 9 can be extended in length during the operation or there can be sticks of various defined preset lengths.
A specific embodiment of a needle-sleeve 24 and needle-sleeve-block 25 is shown in
The needle-sleeve-lock-in mechanism 26 allows a fast, safe and easy connection of the needle holder in the positioning device. Mechanical fixation 41 allows a precise lock-in in the longitudinal axis of the needle-sleeve-block 25. The mechanical fixation mechanism 42 has a squared cross section to prevent rotation of the needle-sleeve-block 25. The locking lever 43 fits into the mechanical fixation 41 at the opposite site.
The subject invention also relates to other techniques to make the needle sleeve visible for the MRI scanner. Fiducial markers, or other markers that use for example overhauser or electron spin can be incorporated. Two or three of these markers can exactly define the position of the needle sleeve and the way the needle will go. To save time it is possible to take a high resolution 3-D-image first and use the needle guide only to navigate. This has the advantage of fast nice pictures of the lesion in real time. For safety reasons it might be desirable to take at least one image with the needle guide in place.
The biopsy needle can slide through inner tube 28, which can be aligned parallel to the outer tube 27. The inner diameter and length of tube 28 can match the outer diameter of the biopsy needle used. Typically the inner diameter is 8 to 16 G (gauge) or 1.7 to 3.0 mm. The needle-sleeve-block 25 with needle-sleeve 24 can be adapted to the needle-sleeve-holder 22 of the reusable prostate-biopsy system by, for example, a snap-on mechanism 31. For better orientation, the needle sleeve block can be filled with material which can produce contrast to show up in the image and indicate the axis of rotation of screw 50. In a specific embodiment, the needle sleeve can be made of materials substantially invisible to magnetic resonance imaging and a needle which is visible can be used.
The system incorporating the needle-sleeve 24 and its sub-parts, the needle-sleeve-block 25, and the snap-on mechanism 31 can be made as one disposable part. This system can utilize plastic parts. Examples of plastic which can be utilized include but are not limited to, PE, PP, PU, PEEK or TEFLON (i.e. polytetrafluoroethylene (PTFE)). Ceramic or low artifact giving metals, such as titanium and titanium-alloys can also be used.
Another specific embodiment of the subject invention is shown in
This example describes a method for affecting a biopsy in accordance with the subject invention. In a specific embodiment, the subject prostate-biopsy-device can be operated in conjunction with a body faced array coil taking 6 to 8 samples, for example, by implementing the following:
Position the patient and the subject prostate-biopsy-device. Lay the patient prone on the stabilization pillow.
Install the body faced array coil, and the arm of the prostate biopsy device.
Insert the needle-sleeve through the anus onto the inner wall of the intestine posterior to the prostate (left apical corner of the prostate a).
Move the patient with device in the MR magnet and perform a first control scan (axial through prostate and needle sleeve).
Reposition the needle-sleeve if needed by moving the arm of the device from outside by using the sticks or move the patient out of the magnet and reposition manually the appropriate screws.
Measure the depth of the lesion in the prostate via another MR scan. If position is right move the patient out of magnet, introduce the biopsy needle through the needle sleeve into the prostate, and fire the biopsy needle to do the biopsy, or move the patient out of the magnet, introduce the biopsy through the needle sleeve into the prostate, fire the needle, and take a control image with the needle in place. Push out the needle notch, move the patient back into the MR magnet to make a controlling scan, and move the patient out of the magnet, to fire the biopsy needle to do the biopsy. (Or move the patient out of the magnet, introduce the biopsy needle through the needle sleeve into the prostate, drive the patient back into the MR magnet, and fire the biopsy needle to do the biopsy by using a stick from outside to operate the needle.) Alternatively, the hub-tube 45 of the device can be repositioned, so that the needle only penetrates to a certain depth.
Take out the first sample. Move the sliding part of the lower arm 20 by turning adjustment screw 19 to position the needle sleeve in the middle b (referring to
Position the needle guide at the right side of the prostate 5 d (referring to
The procedure described in this example allows a caregiver to take only two to four images to perform safe and fast biopsies with good control of the needle position. T2 weighted sequences can be used to view the prostate 5. After giving contrast media T1, weighted FLASH 3D sequences (SIEMENS 1.5T) can be used. For the intervention itself, a HASTE sequence or a T1 weighted Spin Echo sequence can be used. In a 0.2 T SIEMENS MR tomographer, imaging was accomplished using a FLASH 2D-Sequence (TR/TE=100/9: 70Grad), T2-SE (TR/TE=100/9; 70Grad), and a FISP-Rotated-Keyhole-Sequence (TR/TE=18/8; 90Grad).
Embodiments of the subject invention can use the KM-filled needle guide to be detected under MRI and to be used to guide instruments under MRI. The needle guide can have different sizes and shapes that allow better detection or better recognition under MRI. The shape of the cavity that is filled can have, for example, a round shape, a cylindrical shape with a central aperture to put the needle through, or an irregular shape that can allow detection of all three degrees of freedom, as well as rotation. The use of different shapes can allow differentiation of needle guides from each other if there is more than one needle guide used at the same a time. In addition, software can be used to automatically detect the position of the needle sleeve and to use this information to control the MRI scanner. Transfer of this information to the scanner to acquire the MR-signal of the needle sleeve can be enhanced by adding self-resonating LC-circuits or small active coils. Both techniques can help to detect the needle guide with the MR-scanner and automatically detect the instrument track. Resonating or active coils of different size and shape can help differentiate the needle sleeves and make localization faster and more accurate.
To position an instrument in a moving organ such as a liver or a lung, a more flexible holding arm can be utilized and a connector for interconnection with sterile positioning units can be incorporated.
Referring to
In this case, the positioning unit carries an adjustable ball-shaped needle guide 65 that is pushed against the skin and can allow insertion and guiding of an instrument. The S-shaped fixation arms 66 allow the ball to be placed directly on the skin and to have area for a loop-coil to improve images in the region of interest. This imaging coil can also be integrated in the fixation arms or connected to them. This coil can also be used as a positioning coil as it is close to the needle guide and can detect the position and direction of the needle sleeve by using a special sequence that correlates with the filling and configuration of the needle guide to give clear signals.
An embodiment of the subject invention can allow clamping of the ball-shaped needle guide 65, which can contain KM filling or can be connected to a needle guide of, for example, a cylindrical or other shape. The screw 67 allows free rotation and clamping of the ball. If the screw is opened further, the ball can be released completely to allow free motion by an easy-release mechanism. For example, the ball can take disposable needle sleeves that are currently used for breast biopsies with integrated clamping, and can also take bone biopsy devices or instruments such as endoscopes.
It is possible to steer the MR-imaging plane by the needle guide with real time imaging. The needle guide is detected by an automated detection software, as known in the art, which can provide the MR scanner the direction and position of the imaging plane. If the instrument is in the correct position, the MR scanner can automatically generate a control scan that shows the instrument and the surrounding anatomy.
It is also possible to use the MR scanner as a navigation system to detect the needle guide and to overlay the theoretical position from a prior detected dataset. This can allow pre-adjustment and the ability to take a confirmation scan to see if the instrument can be inserted safely.
MR-detectable markers can be integrated in the holding arm, the connector, the positioning unit, in the needle guide, or integrated in the Instrument. Techniques for connecting markers with the instruments is well known in the art and can be utilized in accordance with the subject invention.
The holding arm can carry different positioning systems, such as one for a prostate or one with the ball-shaped needle guide for a liver as described above. The holding arm can also carry a y-x positioning unit or a grid-plate. The conical connector can carry a frame that may have an integrated coil and can carry the grid-plate, as shown in
The frame can carry fiducial markers that can be recognized by software, such as DynaCad™, to determine the exact needle position or needle guide position, which can be used to adjust and to visualize the needle track before the needle is inserted.
The fast connector allows the exchange of positioning units as well as the use of marker-plates to form different navigation systems, and allow the combination of these solutions. In this way, it is possible to define the position with an optical or other navigation system outside the magnet or to reference the arm position and to make adjustments with the positioning unit.
In addition, to make these positioning capabilities more effective, it is often desirable to have very little patient movement. This can be achieved by using a vacuum mattress to fix the extremities, for example. This mattress can be connected to the base of the holding arm.
All patents, patent applications, provisional applications, and publications referred to or cited herein are incorporated by reference in their entirety, including all figures and tables, to the extent they are not inconsistent with the explicit teachings of this specification.
It should be understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application.
[1] Dan Krotz: “MRI earns praise in prostate screening of high-risk patients” Diagnostic Imaging Europe, March/ April 1999, page 14
[2] Prof. Sylvia Heywang-Köbrunner: “Breast MRI proves worth but lacks standardization” Diagnostic Imaging Europe, May 1999, page 33-41
[3] Michael Perrotti et al: “Predicting likelihood of prostate cancer with magnetic resonance imaging” Journal of Urology, Vol. 162, No. 4, Oct. 1999, page 1314-1317
[4] Matthew D. Rifkin et al: “Comparison of magnetic resonance imaging and ultrasonography in staging early prostate cancer; results of a multi-institutional cooperative trial” The New England Journal of Medicine, Vol. 323, No. 10, Sept. 1999, page 621-623
[5] W. Crone-Münzebrock, V. Nicolas, D. Beyersdorff, G. Witte, R. Maas “Results of CT-guided thorax punctures” Pneumologie 46 (6), 1992, page 226-228
[6] W. Crone-Münzebrock, V. Nicolas, D. Beyersdorff, G. Witte “Results of CT-guided punctures in the abdominal and pelvis region” Aktuelle Radiologie 2 (4), 1992, page 230-233
[7] D. Beyersdorff, J. Bahnsen, H.-J. Frischbier “Nodal involvement in cancer of the uterine cervix: Value of lymphology and MRI” European Journal of Gynaecological Oncology 16 (4), 1995, page 274-277
[8] D. Beyersdorff, V. Nicolas, T. Schiemann, H. Kooijman “Three dimensional model of the male pelvic floor muscles based on CT, MR imaging, and sheet plastination” 82nd Scientific Assembly and Annual Meeting RSNA, 1996
The present application is a continuation-in-part of U.S. application Ser. No. 10/366,831, filed Feb. 14, 2003, which claims the benefit of U.S. Provisional Application Ser. No. 60/357,205, filed Feb. 14, 2002, the present application also claims priority of U.S. Provisional Application Ser. No. 61/016,300, filed Dec. 21, 2007, which are hereby incorporated by reference herein in their entirety, including any figures, tables, or drawings.
Number | Date | Country | |
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60357205 | Feb 2002 | US | |
61016300 | Dec 2007 | US |
Number | Date | Country | |
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Parent | 10366831 | Feb 2003 | US |
Child | 12341748 | US |