Inherited risk for prostate cancer (PCa): Following the natural history of men with increased genetic risk using multiparametric MRI (mpMRI).

A Anna Couvillon (National Institutes of Health, Bethesda, MD) B Baris Turkbey (2Molecular Imaging Branch, NCI, Center for Cancer Research, NIH, Bethesda, United States) P Peter Choyke (2Molecular Imaging Branch, NCI, Center for Cancer Research, NIH, Bethesda, United States) K Katherine Lee-Wisdom Y Yolanda McKinney (Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD) S Sue J. Friedman (Facing Our Risk of Cancer Empowered (Force), Tampa, FL) I Inger Rosner (Inova Health System, Fairfax, VA) R Rebecca Davidson Kaltman (Saville Cancer Screening and Prevention Center, Inova Schar Cancer Institute, Fairfax, VA) R Robert Sidlow (Memorial Sloan Kettering Cancer Center, New York, NY) M Michael P. Mullane (Aurora Cancer Care, Racine, WI) V Veda N. Giri (Yale Cancer Center, Yale School of Medicine, New Haven, CT) T Todd Matthew Morgan (Department of Urology, University of Michigan, Ann Arbor, MI) H Heather H. Cheng (University of Washington, Seattle, WA) M Maria Merino (Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, MD) W William Douglas Figg P Peter A. Pinto (Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD) W William L. Dahut (American Cancer Society Chevy Chase Maryland USA) F Fatima Karzai

Abstract

315 Background: PCa has substantial inherited predisposition and certain germline variants like BRCA1/2 , ATM , HOXB13 , and DNA mismatch repair (MMR) genes are associated with an increased risk of PCa. This study follows men without a diagnosis of PCa, with known germline pathogenic/likely pathogenic variant (PV) in BRCA1/2 , DNA MMR genes associated with Lynch syndrome ( MLH1/PMS2 , MSH2 / MSH6 , EPCAM ), HOXB13 , ATM , CHEK2 , PALB2 , TP53 , NBN , RAD51C/D , BRIP1 , and FANCA-FANCM (NCT03805919). Methods: Up to 500 men, ages 30-75 years old (y/o) with a documented PV will enroll. Men undergo biennial mpMRI and annual PSA. Indication for prostate biopsy includes clinical, PSA, and/or MRI findings. Patients are followed at 12-month intervals to determine PSA, PCa diagnosis, and disease/survival status until death. Results: To date, 378 evaluable patients have enrolled: 353 (93%) Caucasian, 11 (3%) Hispanic, 7 (2%) Asian, 4 (1%) African-American, 2 (1%) bi-ethnic. 1 Indian-Asian. Median age was 47 y/o. The most common PV were: 180 (48%) BRCA2 , 94 (25%) BRCA1 , 22 (6%) CHEK2 , and 18 (5%) ATM . PVs in MLH1 / PMS2 , MSH2 / MSH6 , PALB2 , HOXB13 , TP53 , BRIP1 , RAD51D , EPCAM , NBN , and FANCA are <4%. Eight patients carried more than one PV. A total of 782 MRIs were performed: 378 baselines, 228 at year 2, 121 at year 4, 30 at year 6, and 25 clinical. Indication for biopsy was present in 89 (24%) patients with 37 (10%) diagnosed with PCa. Of the 90 biopsies indicated, 1 refused and withdrew and 3 are still pending. Of those with PCa, 22 had BRCA1/2 PVs, 5 had MMR PVs, and 10 had non-MMR PVs. Median age at diagnosis was 62. 24 patients were diagnosed with Grade Group (GG) 1, 8 patients with GG2, 1 patient with GG3, 3 patients with GG4, 1 patient with GG5. 21 opted for active surveillance (AS), 10 opted for prostatectomy, 6 opted for radiation therapy. 5 patients on AS converted to definitive treatment after progression was noted at 1-year follow-up. Conclusions: mpMRI screening in men with PVs is feasible and can be used for early diagnosis, PCa monitoring, and facilitates PCa diagnosis at PSA levels below conventional thresholds. Correlative studies including cfDNA, PBMCs and PRS, are ongoing. Clinical trial information: NCT03805919 . Indication for biopsy. BiopsyPositive BiopsyNegative Biopsy Pending, Refused Total = 89 PSA WNL PSA Elevated PSA WNL PSA Elevated PSA WNL PSA Elevated PIRADS 1 13 0 4 0 9 0 0 PIRADS 2 15 1 3 5 6 0 0 PIRADS 3 23 5 1 11 3 2 1 PIRADS 4 34 10 9 13 2 0 0 PIRADS 5 4 1 3 0 0 0 0

Article Details

Volume / Issue Vol. 44, Issue 7_suppl
Published March 01, 2026
Pages 315-315
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

A

Anna Couvillon

National Institutes of Health, Bethesda, MD

B

Baris Turkbey

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

P

Peter Choyke

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

K

Katherine Lee-Wisdom

Y

Yolanda McKinney

Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD

S

Sue J. Friedman

Facing Our Risk of Cancer Empowered (Force), Tampa, FL

I

Inger Rosner

Inova Health System, Fairfax, VA

R

Rebecca Davidson Kaltman

Saville Cancer Screening and Prevention Center, Inova Schar Cancer Institute, Fairfax, VA

R

Robert Sidlow

Memorial Sloan Kettering Cancer Center, New York, NY

M

Michael P. Mullane

Aurora Cancer Care, Racine, WI

V

Veda N. Giri

Yale Cancer Center, Yale School of Medicine, New Haven, CT

T

Todd Matthew Morgan

Department of Urology, University of Michigan, Ann Arbor, MI

H

Heather H. Cheng

University of Washington, Seattle, WA

M

Maria Merino

Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, MD

W

William Douglas Figg

P

Peter A. Pinto

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

W

William L. Dahut

American Cancer Society Chevy Chase Maryland USA

F

Fatima Karzai