4.6 Article

Application of the PRECISION Trial Biopsy Strategy to a Contemporary Magnetic Resonance Imaging-Targeted Biopsy Cohort-How Many Clinically Significant Prostate Cancers are Missed?

Journal

JOURNAL OF UROLOGY
Volume 205, Issue 3, Pages 740-747

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/JU.0000000000001406

Keywords

prostatic neoplasms; magnetic resonance imaging; biopsy

Funding

  1. Joseph and Diane Steinberg Charitable Trust
  2. United Kingdom National Institute for Health Research (NIHR)
  3. Medical Research Council
  4. Cancer Research UK
  5. Movember
  6. Prostate Cancer UK
  7. Pierre Brahm family
  8. Urology Care Foundation Research Scholar Award Program
  9. Society for Urologic Oncology Fund for Specialized Program of Research Excellence

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The study demonstrates the generalizability of applying the PRECISION biopsy strategy to a contemporary cohort, resulting in a reduction of Gleason grade group 1 detection rate while potentially missing a small number of clinically significant prostate cancers, typically characterized by small volume, low risk, and Gleason grade group 2. Missed clinically significant prostate cancers are predominantly ipsilateral to the magnetic resonance imaging target, possibly indicating targeting error.
Purpose: To demonstrate the generalizability of PRECISION findings and apply the PRECISION biopsy strategy to a contemporary cohort to characterize cancers missed by employing this strategy. Materials and methods: A total of 629 men biopsied between February 2015 and September 2018 met PRECISION inclusion criteria. Men with PI-RADS (TM) 1-2 magnetic resonance imaging were only biopsied if high clinical suspicion for cancer. Missed cancers were defined as prostate cancer identified uniquely on systematic biopsy in men with PI-RADS 3-5 magnetic resonance imaging, or on either systematic biopsy or magnetic resonance imaging-targeted prostate biopsy in men with PI-RADS 1-2 magnetic resonance imaging. Outcomes included 1) clinically significant prostate cancer, Gleason grade group 2 or greater, detection rate, 2) missed clinically significant prostate cancer rate upon application of PRECISION biopsy strategy, 3) Gleason grade group distribution, core size, spatial orientation and oncologic risk among missed cancers. Results: Application of the PRECISION biopsy strategy to the study cohort resulted in avoidance of biopsy in 28%, similar magnetic resonance imaging-targeted prostate biopsy detection rate to PRECISION, reduction of Gleason grade group 1 detection rate by 60% and reduction of clinically significant prostate cancer detection rate by 19%. Missed clinically significant prostate cancers were often smaller than 6 mm (54.5%), Gleason grade group 2 (67.3%) and low risk by clinical nomogram (74.6%). Gleason grade group 1 cancers identified uniquely on systematic biopsy were often contralateral to magnetic resonance imaging target (46.4%), while missed clinically significant prostate cancer was predominantly ipsilateral (81%). Limitations include biopsy of only men with high risk clinical features among PI-RADS 1-2 magnetic resonance imaging, potentially overestimating the clinically significant prostate cancer detection rate. Conclusions: The study cohort demonstrated generalizability of PRECISION findings. Applying the PRECISION biopsy strategy greatly reduces Gleason grade group 1 detection rate, while missing a small number of clinically significant prostate cancer, typically small volume, low risk, and Gleason grade group 2. Missed clinically significant prostate cancer is predominantly ipsilateral to magnetic resonance imaging target, possibly representing targeting error.

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