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
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
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (27)
Andrew J. Armstrong
Vinnie Y.T. Liu
Artera Inc, Los Altos, CA
Ramprasaath R. Selvaraju
Artera Inc, Los Altos, CA
Emmalyn Chen
Artera Inc, Los Altos, CA
Jeffry P. Simko
UCSF Medical Center, San Francisco, CA
Sandy DeVries
University of California San Francisco, San Francisco, CA
Oliver Sartor
Mayo Clinic Comprehensive Cancer Center Mayo Clinic Rochester Minnesota USA
Howard M. Sandler
Cedars-Sinai Medical Center, Los Angeles, CA
Osama Mohamad
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX
Huei-Chung Huang
Artera Inc, Los Altos, CA
Jacqueline Griffin
Rikiya Yamashita
Artera, Inc., Los Altos, CA
Andre Esteva
Artera, Inc., Los Altos, CA
Phuoc T. Tran
Daniel E. Spratt
John Hi Carson
Saint John Regional Hospital, Saint John, New Brunswick, CA
Christopher Peters
Northeast Radiation Oncology Center, Dunmore, PA accrual for Regional Hospital of Scranton
Elizabeth Gore
Zablocki Veterans Administration Medical Center, Milwaukee, WI
Steve P. Lee
Long Beach VA Healthcare System, Long Beach, CA
Jedidiah M. Monson
Saint Agnes Medical Center, Fresno, CA
Mark E. Augspurger
Baptist Medical Center South, Jacksonville, FL
Ali El-Gayed
Saskatoon Cancer Centre, Saskatoon, SK
Joseph P. Rodgers
NRG Oncology Statistics and Data Management Center, Philadelphia, PA
Rana McKay
Moores Cancer Center
Todd Morgan
University of Michigan, Ann Arbor, MI
Felix Y. Feng
Paul L. Nguyen
Mass General Brigham, Boston