Medical Policy |
Subject: Spectral Analysis of Prostate Tissue by Fluorescence Spectroscopy | |
Document #: SURG.00148 | Publish Date: 04/16/2025 |
Status: Reviewed | Last Review Date: 02/20/2025 |
Description/Scope |
This document addresses the use of spectral analysis of prostate tissue by fluorescence spectroscopy, which involves using fiber optics to differentiate between normal prostate tissue and suspicious prostate tissue.
Note: Please see the following related documents for additional information:
Position Statement |
Investigational and Not Medically Necessary:
Spectral analysis of prostate tissue by fluorescence spectroscopy is considered investigational and not medically necessary for all indications.
Rationale |
Spectral analysis of prostate tissue by fluorescence spectroscopy has been proposed as a method to improve yield of tissue biopsies taken from the prostate. This system uses a predictive algorithm to perform spectral analysis of reflected light to distinguish between normal and suspicious tissue which can then help guide prostate biopsy procedures.
A 2015 feasibility study was reported by Werahera and colleagues. In this study, 13 participants with prostate cancer who were scheduled to undergo radical prostatectomy also consented to have analysis of prostate tissue by fluorescence spectroscopy during the prostatectomy. The primary objective was to evaluate the safety and effectiveness of the optical biopsy needle to acquire spectral data and correlative tissue biopsy cores for real-time diagnosis of prostate cancer in clinical settings. The in vivo optical biopsies were performed during the radical prostatectomy and multiple biopsy core samples and correlative spectral data were obtained from each participant within a 10-minute time period. Following radical prostatectomy, ex vivo biopsy core samples and spectral data were also obtained from each surgically excised prostate within a 90-minute time period. The spectral data and corresponding tissue biopsy cores were obtained from different locations within each prostate specimen. The biopsy cores were classified as either benign or malignant and then correlated with the corresponding spectral data. In the in vivo samples, histopathological analysis found cancer in 29/208 viable biopsy cores and in the ex vivo samples, cancer was reported in 51/224 viable biopsy cores. For the in vivo samples there was 72% sensitivity, 66% specificity, and 93% negative predictive value. For the ex vivo samples there was 75% sensitivity, 80% specificity, and 93% negative predictive value in malignant versus benign prostatic tissue classification. The study shows a potential clinical application of spectral analysis of prostate tissue by fluorescence spectroscopy, however additional studies are necessary to assess improved net health outcomes.
Clinical trials are in progress to collect information on prostate biopsy tissue using fluorescence spectroscopy during radical prostatectomy surgery. At this time, the device does not have United States Food and Drug Administration approval.
Background/Overview |
Prostate cancer is the most commonly diagnosed cancer, other than skin cancers, in North American men. According to the American Cancer Society (ACS), in 2025 there will be an estimated 313,780 new cases of prostate cancer and 35,770 deaths. Prostate cancer is the second leading cause of cancer death in American men, exceeded only by lung cancer. Men in the United States have about 1 chance in 8 of eventually being diagnosed with this malignancy and about 1 man in 44 will eventually die of the disease (ACS, 2025).
The ClariCore™ Biopsy System (Precision Biopsy™, Aurora, CO) is the device for collecting prostate biopsy tissue using fluorescence spectroscopy. According to the manufacturer’s website, the ClariCore system has been licensed by another manufacturer (PreView Medical, Inc., Longmont, CO).
Definitions |
Biopsy: The removal of a sample of tissue for examination under a microscope for diagnostic purposes.
Prostate: A walnut-shaped gland in men that extends around the urethra at the neck of the urinary bladder and supplies fluid that goes into semen.
Radical prostatectomy: Surgical procedure for the removal of the prostate.
Coding |
The following codes for treatments and procedures applicable to this document are included below for informational purposes. Inclusion or exclusion of a procedure, diagnosis or device code(s) does not constitute or imply member coverage or provider reimbursement policy. Please refer to the member's contract benefits in effect at the time of service to determine coverage or non-coverage of these services as it applies to an individual member.
When services are Investigational and Not Medically Necessary:
For the following procedure code or when the code describes a procedure indicated in the Position Statement section as investigational and not medically necessary.
CPT |
|
0443T | Real-time spectral analysis of prostate tissue by fluorescence spectroscopy, including imaging guidance [add-on code] |
|
|
ICD-10 Diagnosis |
|
| All diagnoses |
References |
Peer Reviewed Publications:
Government Agency, Medical Society, and Other Authoritative Publications:
Websites for Additional Information |
Index |
ClariCore Biopsy System
Prostate cancer
Prostatectomy
The use of specific product names is illustrative only. It is not intended to be a recommendation of one product over another, and is not intended to represent a complete listing of all products available.
Document History |
Status | Date | Action |
Reviewed | 02/20/2025 | Medical Policy & Technology Assessment Committee (MPTAC) review. Revised Rationale, Background/Overview, References and Websites for Additional Information sections. |
Reviewed | 02/15/2024 | MPTAC review. Revised Background/Overview, References and Websites for Additional Information sections. |
Reviewed | 02/16/2023 | MPTAC review. Updated Background/Overview, References and Websites for Additional Information sections. |
Reviewed | 02/17/2022 | MPTAC review. Updated Rationale, Background/Overview and References sections. |
Reviewed | 02/11/2021 | MPTAC review. Updated Description/Scope, Rationale, Background/Overview, References, and Websites for Additional Information sections. |
Reviewed | 02/20/2020 | MPTAC review. Updated References section. |
Reviewed | 03/21/2019 | MPTAC review. |
Reviewed | 03/20/2019 | Hematology/Oncology Subcommittee review. Updated Background/Overview and References sections. |
Reviewed | 05/03/2018 | MPTAC review. |
Reviewed | 05/02/2018 | Hematology/Oncology Subcommittee review. The document header wording updated from “Current Effective Date” to “Publish Date.” Updated Background/Overview and References sections. |
New | 05/04/2017 | MPTAC review. |
New | 05/03/2017 | Hematology/Oncology Subcommittee review. Initial document development. |
Applicable to Commercial HMO members in California: When a medical policy states a procedure or treatment is investigational, PMGs should not approve or deny the request. Instead, please fax the request to Anthem Blue Cross Grievance and Appeals at fax # 818-234-2767 or 818-234-3824. For questions, call G&A at 1-800-365-0609 and ask to speak with the Investigational Review Nurse.
Federal and State law, as well as contract language, including definitions and specific contract provisions/exclusions, take precedence over Medical Policy and must be considered first in determining eligibility for coverage. The member’s contract benefits in effect on the date that services are rendered must be used. Medical Policy, which addresses medical efficacy, should be considered before utilizing medical opinion in adjudication. Medical technology is constantly evolving, and we reserve the right to review and update Medical Policy periodically.
No part of this publication may be reproduced, stored in a retrieval system or transmitted, in any form or by any means, electronic, mechanical, photocopying, or otherwise, without permission from the health plan.
© CPT Only – American Medical Association