Development and Validation of an Artificial Intelligence Digital Pathology Biomarker to Predict Benefit of Long-Term Hormonal Therapy and Radiotherapy in Men With High-Risk Prostate Cancer Across Multiple Phase III Trials

A Andrew J. Armstrong V Vinnie Y.T. Liu (Artera Inc, Los Altos, CA) R Ramprasaath R. Selvaraju (Artera Inc, Los Altos, CA) E Emmalyn Chen (Artera Inc, Los Altos, CA) J Jeffry P. Simko (UCSF Medical Center, San Francisco, CA) S Sandy DeVries (University of California San Francisco, San Francisco, CA) O Oliver Sartor (Mayo Clinic Comprehensive Cancer Center Mayo Clinic Rochester Minnesota USA) H Howard M. Sandler (Cedars-Sinai Medical Center, Los Angeles, CA) O Osama Mohamad (Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX) H Huei-Chung Huang (Artera Inc, Los Altos, CA) J Jacqueline Griffin R Rikiya Yamashita (Artera, Inc., Los Altos, CA) A Andre Esteva (Artera, Inc., Los Altos, CA) P Phuoc T. Tran D Daniel E. Spratt J John Hi Carson (Saint John Regional Hospital, Saint John, New Brunswick, CA) C Christopher Peters (Northeast Radiation Oncology Center, Dunmore, PA accrual for Regional Hospital of Scranton) E Elizabeth Gore (Zablocki Veterans Administration Medical Center, Milwaukee, WI) S Steve P. Lee (Long Beach VA Healthcare System, Long Beach, CA) J Jedidiah M. Monson (Saint Agnes Medical Center, Fresno, CA) M Mark E. Augspurger (Baptist Medical Center South, Jacksonville, FL) A Ali El-Gayed (Saskatoon Cancer Centre, Saskatoon, SK) J Joseph P. Rodgers (NRG Oncology Statistics and Data Management Center, Philadelphia, PA) R Rana McKay (Moores Cancer Center) T Todd Morgan (University of Michigan, Ann Arbor, MI) F Felix Y. Feng P Paul L. Nguyen (Mass General Brigham, Boston)

Abstract

PURPOSE Long-term androgen deprivation therapy (ADT) improves survival in men with high-risk localized prostate cancer (PCa) receiving radiotherapy (RT). Predictive biomarkers are needed to guide ADT duration. METHODS A multimodal artificial intelligence (MMAI)–derived predictive biomarker was trained for long-term (LT) versus short-term (ST) ADT using pretreatment digital prostate biopsy images and clinical data (age, prostate-specific antigen, Gleason, and T stage) from six NRG Oncology phase III randomized radiotherapy trials. The novel MMAI-derived biomarker was developed to predict the differential benefit of LT-ADT on the primary end point, distant metastasis (DM). MMAI predictive utility was validated on a seventh randomized trial, RTOG 9202 (N = 1,192), which randomly assigned men to RT + ST-ADT (4 months) versus RT + LT-ADT (28 months). Fine-Gray and cumulative incidence analyses for DM, and secondarily, death with DM, were performed. Deaths without DM were treated as competing risks. RESULTS In the validation cohort (median follow-up, 17.2 years), LT-ADT significantly improved DM from 26% to 17% (subdistribution hazard ratio [sHR], 0.64 [95% CI, 0.50 to 0.82], P < .001). A significant biomarker-treatment predictive interaction was observed ( P = .04) for DM, whereby MMAI biomarker–positive men (n = 785, 66%) had reduced DM with LT-ADT versus ST-ADT (sHR, 0.55 [95% CI, 0.41 to 0.73], P < .001), whereas no treatment benefit was observed for MMAI biomarker–negative men (n = 407; sHR, 1.06 [95% CI, 0.61 to 1.84], P = .84). The estimated 15-year DM risk difference between RT + LT-ADT and RT + ST-ADT was 14% in MMAI biomarker–positive men and 0% in MMAI biomarker–negative men. The MMAI biomarker was also prognostic for DM, irrespective of treatment (sHR, 2.35 [95% CI, 1.72 to 3.19], P < .001). CONCLUSION To our knowledge, the MMAI model is the first validated predictive biomarker to guide ADT duration with RT in localized/locally advanced PCa. Approximately one third of men with high-risk PCa could safely be spared the additional 24 months of ADT and the associated morbidity.

Article Details

Volume / Issue Vol. 43, Issue 32
Published November 10, 2025
Pages 3494-3504
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (27)

A

Andrew J. Armstrong

V

Vinnie Y.T. Liu

Artera Inc, Los Altos, CA

R

Ramprasaath R. Selvaraju

Artera Inc, Los Altos, CA

E

Emmalyn Chen

Artera Inc, Los Altos, CA

J

Jeffry P. Simko

UCSF Medical Center, San Francisco, CA

S

Sandy DeVries

University of California San Francisco, San Francisco, CA

O

Oliver Sartor

Mayo Clinic Comprehensive Cancer Center Mayo Clinic Rochester Minnesota USA

H

Howard M. Sandler

Cedars-Sinai Medical Center, Los Angeles, CA

O

Osama Mohamad

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX

H

Huei-Chung Huang

Artera Inc, Los Altos, CA

J

Jacqueline Griffin

R

Rikiya Yamashita

Artera, Inc., Los Altos, CA

A

Andre Esteva

Artera, Inc., Los Altos, CA

P

Phuoc T. Tran

D

Daniel E. Spratt

J

John Hi Carson

Saint John Regional Hospital, Saint John, New Brunswick, CA

C

Christopher Peters

Northeast Radiation Oncology Center, Dunmore, PA accrual for Regional Hospital of Scranton

E

Elizabeth Gore

Zablocki Veterans Administration Medical Center, Milwaukee, WI

S

Steve P. Lee

Long Beach VA Healthcare System, Long Beach, CA

J

Jedidiah M. Monson

Saint Agnes Medical Center, Fresno, CA

M

Mark E. Augspurger

Baptist Medical Center South, Jacksonville, FL

A

Ali El-Gayed

Saskatoon Cancer Centre, Saskatoon, SK

J

Joseph P. Rodgers

NRG Oncology Statistics and Data Management Center, Philadelphia, PA

R

Rana McKay

Moores Cancer Center

T

Todd Morgan

University of Michigan, Ann Arbor, MI

F

Felix Y. Feng

P

Paul L. Nguyen

Mass General Brigham, Boston