Outcomes of high-risk prostate-specific antigen level during active surveillance with targeted and systematic prostate biopsy.

B Braden Millan (Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD) J Jaskirat Saini (Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD) M Mitchell J. Hwang (Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD) C Charles Hesswani (Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD) R Ruben Blachman-Braun (National Institutes of Health, Bethesda, MD) C Christopher R Koller (Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD) D Daniel Nethala (Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD) B Brad Wood (Center for Interventional Oncology, National Cancer Institute, National Institutes of Health, Bethesda, MD) B Baris Turkbey (2Molecular Imaging Branch, NCI, Center for Cancer Research, NIH, Bethesda, United States) S Sandeep Gurram (Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD) P Peter A. Pinto (Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD)

Abstract

343 Background: National Comprehensive Cancer Network (NCCN) recommendations for very low to intermediate-risk prostate cancer (PCa) include active surveillance (AS). Patients who develop a prostate-specific antigen (PSA) level over 20 ng/mL during AS, however, are re-classified as NCCN high-risk and are recommended to undergo definitive management. In the past decade, the diagnostic accuracy for PCa has significantly improved with a combined approach to prostate biopsies (magnetic resonance imaging and ultrasound fusion targeting + systematic). This study aims to describe the outcomes of patients who continued AS following a PSA of 20 ng/mL or higher. Methods: Patient information and clinical data were obtained from a prospectively maintained database at the National Cancer Institute (NCT02594202). Patients on AS with a minimum of one subsequent combined biopsy (fusion + systematic) following a PSA of 20 ng/mL or higher were identified. Descriptive statistics were obtained using GraphPad Prism 10.1 (Boston, Massachusetts USA). Results: A total of 20 patients were identified, of whom 15 (67.7%) subsequently underwent definitive management. Patients had a median age of 72.0 [IQR 71-74.8] years, with a median of 13 [IQR 10-12] years on AS. In the continued AS cohort, the most recent PSA was below 20 ng/mL in two patients with a median of 22.9 ng/mL [IQR 15.2 -23.6], while repeat biopsy showed benign tissue or grade group (GG) 1 disease. In those who underwent definitive management, the last PSA on AS was a median of 23.2 ng/mL [IQR 21.9-32.8], with all patients having GG 2 or higher disease. Twelve patients underwent surgery and three external beam radiotherapy with long-term androgen deprivation therapy, within a median time of 2 mos [IQR 2.0 - 2.5 mos] after their last biopsy. For those who underwent surgery, 4 (33.3%) had GG upstaging, 2 (16.7%) had GG downstaging, while 6 (50.0%) had no change in overall GG on final pathology. The first post-operative PSA was undetectable in all but one patient. Conclusions: A PSA greater than 20 ng/mL is a high-risk feature that continues to have clinical significance during AS in the contemporary era of combined prostate biopsies. In our small cohort, one quarter of the patients remain on AS, while three-quarters of the patients underwent definitive management. GG upgrading occurred in one third of patients and therefore continued AS in these patients should be approached with caution and limited to those with benign findings or GG 1 disease on follow-up combined biopsy.

Article Details

Volume / Issue Vol. 43, Issue 5_suppl
Published February 10, 2025
Pages 343-343
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (11)

B

Braden Millan

Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD

J

Jaskirat Saini

Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD

M

Mitchell J. Hwang

Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD

C

Charles Hesswani

Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD

R

Ruben Blachman-Braun

National Institutes of Health, Bethesda, MD

C

Christopher R Koller

Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD

D

Daniel Nethala

Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD

B

Brad Wood

Center for Interventional Oncology, National Cancer Institute, National Institutes of Health, Bethesda, MD

B

Baris Turkbey

2Molecular Imaging Branch, NCI, Center for Cancer Research, NIH, Bethesda, United States

S

Sandeep Gurram

Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD

P

Peter A. Pinto

Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD