Magnetic Resonance Imaging-Guided Biopsy in Active Surveillance of Prostate Cancer
Purpose:The underlying premise of prostate cancer active surveillance (AS) is that cancers likely to metastasize will be recognized and eliminated before cancer-related disease can ensue. Our study was designed to determine the prostate cancer upgrading rate when biopsy guided by magnetic resonance...
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Published in | The Journal of urology Vol. 207; no. 4; pp. 823 - 831 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Philadelphia, PA
Wolters Kluwer
01.04.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Purpose:The underlying premise of prostate cancer active surveillance (AS) is that cancers likely to metastasize will be recognized and eliminated before cancer-related disease can ensue. Our study was designed to determine the prostate cancer upgrading rate when biopsy guided by magnetic resonance imaging (MRGBx) is used before entry and during AS.Materials and Methods:The cohort included 519 men with low- or intermediate-risk prostate cancer who enrolled in prospective studies (NCT00949819 and NCT00102544) between February 2008 and February 2020. Subjects were preliminarily diagnosed with Gleason Grade Group (GG) 1 cancer; AS began when subsequent MRGBx confirmed GG1 or GG2. Participants underwent confirmatory MRGBx (targeted and systematic) followed by surveillance MRGBx approximately every 12 to 24 months. The primary outcome was tumor upgrading to ≥GG3.Results:Upgrading to ≥GG3 was found in 92 men after a median followup of 4.8 years (IQR 3.1-6.5) after confirmatory MRGBx. Upgrade-free probability after 5 years was 0.85 (95% CI 0.81-0.88). Cancer detected in a magnetic resonance imaging lesion at confirmatory MRGBx increased risk of subsequent upgrading during AS (HR 2.8; 95% CI 1.3-6.0), as did presence of GG2 (HR 2.9; 95% CI 1.1-8.2) In men who upgraded ≥GG3 during AS, upgrading was detected by targeted cores only in 27%, systematic cores only in 25% and both in 47%. In 63 men undergoing prostatectomy, upgrading from MRGBx was found in only 5 (8%).Conclusions:When AS begins and follows with MRGBx (targeted and systematic), upgrading rate (≥GG3) is greater when tumor is initially present within a magnetic resonance imaging lesion or when pathology is GG2 than when these features are absent. |
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Bibliography: | Correspondence: Department of Urology, David Geffen School of Medicine, UCLA, Wasserman Bldg., 3rd Floor, Los Angeles, California 90095 telephone: 310-794-3070; FAX: 310-794-0987; lmarks@mednet.ucla.eduSupport: Supported in part by R01CA218547, R01CA195505, the Intramural Research Program of the National Cancer Institute, the Center for Interventional Oncology, intramural NIH Grants Z1A CL040015, 1ZIDBC011242, UL1TR000124 from University of California, Los Angeles Clinical and Translational Science Institute, the University Hospital Foundation in Edmonton, Alberta, and generous donation from Mr. Leo Broks.Disclosures: NIH and Philips have a Cooperative Research and Development Agreement.Conflict of Interest: Dr. Marks is co-founder of Avenda Health. Dr. Priester is data scientist at Avenda Health.Licensed Patents/Royalties: Philips: NIH receives royalties for licensed patents from Philips and in turn, BW, BT, PP, PC receive resulting royalties from NIH. NIH may own intellectual property in the field (multiple patents and patents pending-available upon request).Intellectual Property: NIH & BW.Non-Endorsement Language: The content of this manuscript does not necessarily reflect the views, policies, or opinions of the U.S. Department of Health and Human Services. The mention of commercial products, their source, or their use in connection with material reported herein is not to be construed as an actual or implied endorsement of such products by the United States government. Opinions expressed are those of the authors, not necessarily the NIH nor the NCI.*Equal study contribution.Editor's Note: This article is the third of 5 published in this issue for which category 1 CME credits can be earned. Instructions for obtaining credits are given with the questions on pages 944 and 945. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Equal study contribution. |
ISSN: | 0022-5347 1527-3792 1527-3792 |
DOI: | 10.1097/JU.0000000000002343 |