Colonic polyp discrimination by tissue fluorescence and fiberoptic probe

Abstract

A system and method for the in situ discrimination of healthy and diseased tissue. A fiberoptic based probe is employed to direct ultraviolet illumination onto a tissue specimen and to collect the fluorescent response radiation. The response radiation is observed at three selected wavelengths, about 403 nm, about 414 nm, and about 431 nm. The intensities of the 403 nm and 414 mn radiation are normalized using the 431 nm intensity. A score is determined using the ratios in a linear discriminant analysis (LDA). The tissue under examination is resected or not, based on the outcome of the LDA.

Description

FIELD OF THE INVENTION

This invention relates generally to diagnosis of disease. More particularly, the invention relates to in situ diagnosis by optical methods.

BACKGROUND OF THE INVENTION

Polyps of the colon are very common. There are two major types of colonic polyps, neoplastic and non-neoplastic. Non-neoplastic polyps are entirely benign with no malignant potential and do not necessarily need to be resected. Hyperplastic polyps, juvenile polyps, mucosal prolapse and normal mucosal polyps are examples of non-neoplastic polyps. Conversely, neoplastic polyps are pre-malignant, a condition requiring resection and further surveillance. Examples of premalignant neoplastic polyps are tubular adenoma, villous adenoma and tubulovillous adenoma.

Conventional laser-induced fluorescence emission and reflectance spectroscopy can distinguish between neoplastic and non-neoplastic tissue with accuracies approaching about 85%. However, typically these methods require that the full spectrum be measured with algorithms dependent on many emission wavelengths.

SUMMARY OF THE INVENTION

This invention, in one embodiment, relates to an optical probe and methods for identifying neoplastic polyps of the colon during endoscopy or colonoscopy. In one embodiment, the probe comprises 6 collection fibers surrounding a single illumination fiber placed directly in contact with tissue. In one embodiment, a method of the invention comprises laser induced fluorescence using 337 nm excitation and a threshold classification model that depends on two fluorescence intensity ratios: the intensity at about 403 nm divided by the intensity at about 431 nm and the intensity at about 414 nm divided by the intensity at 431 nm. The invention enables determining whether a polyp is neoplastic. Of particular interest, the invention enables such determination at the time of endoscopy particularly for diminutive polyps. In a preferred embodiment, the invention provides for identification of polyps under about 10 mm in size. The invention provides methods that reliably distinguish between neoplastic and non-neoplastic polyps at the time of endoscopy or colonoscopy. As a result, patients with non-neoplastic polyps are not subjected to the risk and expense of polypectomy.

The foregoing and other objects, aspects, features, and advantages of the invention will become more apparent from the following description and from the claims.

BRIEF DESCRIPTION OF THE DRAWINGS

The objects and features of the invention can be better understood with reference to the drawings described below. The drawings are not necessarily to scale, emphasis instead generally being placed upon illustrating the principles of the invention. In the drawings, like numerals are used to indicate like parts throughout the various views.

FIG. 1 is a schematic diagram showing an embodiment of the apparatus according to principles of the invention;

FIG. 2 is a plot of the normalized fluorescence spectra of normal colon, neoplastic polyps and non-neoplastic polyps, according to an embodiment of the invention;

FIG. 3 is a flow diagram showing the steps of the analytical method according to principles of the invention; and

FIG. 4 is a graph showing polyp classification results obtained using a linear discriminant analysis according to principles of the invention.

DETAILED DESCRIPTION

Instrument

The invention in one embodiment involves delivering 337 nm excitation light to tissue via a single optical fiber and collecting remitted light with a plurality of optical fibers surrounding the illumination fiber. The apparatus 100 used in the embodiment is shown in FIG. 1. The apparatus 100 shown in FIG. 1 includes a source 110 of 337 nm illumination as the excitation. The excitation illumination is introduced into an optical fiber 120 for delivery to the tissue under examination. The illumination fiber 120 can be tapered starting at about 0.4 mm in diameter at the proximal end and ending at about 0.1 mm at its distal end. In the present embodiment, a plurality of optical fibers 130 are used to collect the response signal from the tissue under examination. In one embodiment, six collection fibers 130 are placed in an hexagonal array about the central optical fiber 120 that carries the excitation illumination. This geometry is termed herein the “six-around-one fiberoptic probe.” The collection fibers are about 0.1 mm in diameter. The fiberoptic catheter 140 is delivered through the accessory port 150 of a typical endoscope 160 with the distal tip 170 gently touching tissue 180 to be examined. The returned light is separated into fluorescence bands at 403, 414 and 431 nm using a wavelength dispersive element 190 such as a spectrograph or dichroic filter system. The width of the bands should preferably be under 5 nm. The two intensity ratios (I₄₀₃/I₄₃₁ and I₄₁₄/I₄₃₁) are then formed and inputted in a linear discriminant analysis (LDA) threshold model to produce a score. The polyp is removed or left in place based on the sign of the score.

The invention involves illuminating a specimen, such as an in vivo specimen, using illumination having a first wavelength, and observing a response signal, such as a fluorescent response. The response signal is sampled at at least a second wavelength, a third wavelength, and a fourth wavelength. The intensity of the response signal at the second wavelength and at the third wavelength is normalized using the intensity at the fourth wavelength. The normalized responses are used at input values for a discrimination function analysis. The output of the discrimination function analysis is an indication that the specimen examined is healthy or is diseased.

Referring to FIG. 2, a plot 200 depicting a plurality of response spectra is shown, for different tissue types illuminated with the same 337 nm excitation illumination. The spectra observed correspond to tissues including normal colon 210, non-neoplastic polyps 220, and neoplastic polyps 230. The spectra 210, 220, 230 shown in FIG. 2 were recorded with the six-around-one fiberoptic probe.

Changes in optical properties of collagen and blood are the predominant factors in diagnostic differentiation among normal tissue, non-neoplastic polyps, and neoplastic polyps. An algorithm that treats collagen fluorescence, having a peak at about 403 nm in the system of the invention, and hemoglobin absorption, having a peak at about 414 nm for oxyhemoglobin, is sensitive to these changes.

Collagen and blood reside underneath the superficial cellular layer. A fiberoptic geometry designed to probe deeper into tissue but not too deep is more sensitive to changes in collagen and blood and hence in differentiating between polyps types. The six-around-one fiberoptic probe used according to principles of the invention probes deeper into tissue than does a single fiber system.

Interpatient variability in the intensity of fluorescent response is typically large and effects the diagnostic accuracy of techniques based on absolute fluorescence intensities. Historically, effective diagnostic algorithms have used some form of normalization to reduce interpatient variability. One common approach that has been used is to preprocess the data by normalizing the area under each fluorescence spectrum to unity. However, this approach requires that the entire fluorescence spectrum be measured to calculate the area to be used for the normalization factor. The necessity to record an entire spectral response simply to be able to obtain normalization data is redundant and inefficient. The inefficiency is particularly acute if only the emissions at 1 or 2 wavelengths are to be analyzed.

According to the invention, an intensity at a location such as at about 431 nm, between the fluorescence spectra of normal tissue, hyperplastic polyps and adenomatous polyps, is used as a normalization factor that provides effective normalization while requiring fluorescence to be measured at only one addition emission wavelength.

The combination of a new design of a fiberoptic probe for making measurements, an analytic method based on a small number of data points, and a simple method of obtaining a normalization factor for the data used provides enhanced diagnostic accuracy in distinguishing between neoplastic and non-neoplastic polyps. The efficacy of the new system and method is demonstrated in a single-center prospective clinical trial. A higher fraction of polyps were correctly classified with this technique, (e.g., accuracy=86%) when compared to other approaches. The accuracy of the method using two emission wavelengths is better than that obtained in retrospective clinical trials requiring many more wavelengths.

Analysis Method

FIG. 3 is a flow diagram 300 showing the steps of the analytical method. The method involves observing fluorescent intensities at about 403, about 414 and about 431 nm, as shown at step 310. The ratio of the intensity at about 403 nm to that at about 431 nm (I₄₀₃/I₄₃₁), and the ratio of the intensity at about 414 nm to that at about 431 nm (I₄₁₄/I₄₃₁) are formed, as indicated at step 320. The two ratios are then examined by comparison to a linear discrimination function, using linear discrimination analysis (LDA), as shown at step 330. A score value greater than zero is indicative of neoplasia, while a score value less than zero indicates non-neoplasia. Resection can be performed, or omitted, based on the score value that is obtained. Result 340 represents performing resection, while result 350 represents not performing resection.

Sensitivity Analysis

FIG. 4 is a graph 400 showing polyp classification results obtained using a linear discriminant analysis. One hundred and fifty patients were enrolled in a prospective study in which 94 polyps were collected from 50 patients. In FIG. 4, the about 403 nm to about 431 nm fluorescence intensity ratio (I₄₀₃/I₄₃₁) was plotted along the vertical axis 402 against the about 414 nm to about 431 nm ratio (I₄₁₄/I₄₃₁) plotted along the horizontal axis 404 for a given polyp. The LDA threshold discrimination model is depicted as the line 410 in FIG. 4 where polyps corresponding to data points that lie above the line 410 are classified as neoplastic polyps and polyps corresponding to data points that lie below the line 410 are classified as non-neoplastic polyps. Using this model, 47 of 52 neoplastic polyps and 34 of 42 non-neoplastic polyps were classified correctly resulting in a sensitivity and specificity of 90% and 81%, respectively. In addition, 80 of 86 normal colonic tissue sites and 3 of 3 frank adenocarcinomas were correctly classified.

Potential Cost Savings

The ability to identify and distinguish benign and malignant polyps in situ could result in substantial cost savings. In this particular example, 39 of 94 polyps would have been spared from being resected and biopsied, representing a 41% savings in surgical and pathology charges. However, at present there is a false negative rate of 9.6%. The long term outcome of not resecting these polyps will need to be determined. In comparison, other techniques spared 14% of the polyps from being biopsied and had a false negative rate of 0.9%. If polyps greater than 5 mm in the latter study are excluded from this analysis, then 27% of the polyps would not have been biopsied and the technique would have a 3.2% false negative rate.

Application to Other Tissues

The system and method of the invention has been shown to work in colonic tissue. The invention, involving a new probe design and analytical method, can enhance the accuracy for identifying neoplasia in other tissues such as the esophagus, urinary bladder, oral cavity, bronchotracheal tree and cervix.

EQUIVALENTS

While the invention has been particularly shown and described with reference to specific preferred embodiments, it should be understood by those skilled in the art that various changes in form and detail may be made therein without departing from the spirit and scope of the invention.

Claims

1. A method of identifying a state of health of a tissue in vivo, the method comprising the steps of: illuminating a tissue in vivo with light having a wavelength of about 337 nanometers; receiving from the tissue a response comprising fluorescent light having wavelengths of about 403 nanometers, about 414 nanometers, and about 431 nanometers; computing a first ratio, the first ratio being an intensity of the fluorescent light having a wavelength of about 403 nanometers divided by an intensity of the fluorescent light having a wavelength of about 431 nanometers; computing a second ratio, the second ratio being an intensity of the fluorescent light having a wavelength of about 414 nanometers divided by the intensity of the fluorescent light having a wavelength of about 431 nanometers; and deducing a state of health of the tissue depending on the magnitude of the first ratio and the magnitude of the second ratio to a linear discrimination function.

2. The method of claim 1, wherein illuminating the tissue involves contacting the tissue with an illumination optical fiber.

3. The method of claim 1, wherein receiving from the tissue a response comprising fluorescent light involves contacting the tissue with a receiving optical fiber.

4. The method of claim 1, wherein the tissue in vivo comprises a polyp under about 10 millimeters in size.

5. The method of claim 1, wherein deducing a state of health of the tissue comprises deducing the state of health in real time.

6. A system for identifying a state of health of a tissue in vivo, comprising: an illumination source for illuminating a tissue in vivo with light having a wavelength of about 337 nanometers, the source comprising an illuminating optical fiber; a detector for receiving from the tissue a response comprising fluorescent light having wavelengths of about 403 nanometers, about 414 nanometers, and about 431 nanometers, the detection system comprising at least one optical fiber for receiving the fluorescent light; a wavelength dispersive element for separating the fluorescent light into different wavelengths; a computation system for computing a first ratio and a second ratio, the first ratio being an intensity of the fluorescent light having a wavelength of about 403 nanometers divided by an intensity of the fluorescent light having a wavelength of about 431 nanometers, the second ratio being an intensity of the fluorescent light having a wavelength of about 414 nanometers divided by the intensity of the fluorescent light having a wavelength of about 431 nanometers; and an analysis module for deducing a state of health of the tissue depending on the magnitude of the first ratio and the magnitude of the second ratio to a linear discrimination function.

7. The system of claim 6, wherein the illuminating optical fiber contacts the tissue.

8. The system of claim 6, wherein the at least one optical fiber for receiving the fluorescent light contacts the tissue.

9. The system of claim 6, wherein the tissue in vivo comprises a polyp under about 10 millimeters in size.

10. The system of claim 6, wherein the analysis module produces information about the state of health in real time.