Risk of fracture following androgen receptor pathway inhibitors (ARPIs): A population-based study.

G Grace L. Lu-Yao (Thomas Jefferson University, Philadelphia, PA) S Scott W. Keith (Division of Biostatistics, Department of Pharmacology & Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA) K Krupa Gandhi (Division of Biostatistics, Department of Pharmacology & Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA) H Hushan Yang (Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA) A Amy L. Shaver (Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA) N Nikita Nikita (Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA) W William Kevin Kelly (Thomas Jefferson University Hospital, Philadelphia, PA)

Abstract

11164 Background: Androgen deprivation therapy is associated with an increased risk of fracture. ARPIs are widely used to manage advanced prostate cancer (PCa). However, there is limited long-term data on fracture risk following ARPIs and how the risk might vary with different health conditions. This study aims to fill these gaps. Methods: This study used the SEER-Medicare linked files to identify men diagnosed with PCa between 1/1/1999 and 12/31/2019 and who received abiraterone with prednisone (AAP) or enzalutamide (ENZA) between 1/1/2013 and 12/31/2020. The primary endpoint is the time to first fracture after the index date (first date of AAP or ENZA). The history of fracture was based on claims one year before the index date. Fine and Gray’s sub-distribution hazard model was used to estimate the effect of various risk factors. We used the cumulative incidence function to quantify fracture risk. Results: This study comprised 10,463 patients (6,037 with AAP and 4,426 with ENZA). Most patients were over 75 with a comorbidity score of 1 or higher. Among 1,445 patients who had a fracture the year before the index date, the risk of fracture after ARPI reached 50% (95% CI 47% - 53%) within 3 years, compared to 26% (95% CI 25%-27%) among those without a fracture. After adjusting for bone health agent use, comorbidities, and sociodemographic factors, a history of fracture was associated with 2.8 fold risk of fracture after AAP (RR=2.80, 95% CI 2.47 – 3.18) and 2.85 fold risk after ENZA (RR=2.85, 95% CI 2.45-3.30). Use of bone health agents within 3 months before the index date was associated with a 20-25% lower fracture risk. Conclusions: This large population-based study shows that the risk of fracture following ARPIs is substantial, especially among those who suffered a fracture before ARPIs. It is crucial to consider the history of fracture when making treatment choices and monitoring strategies. Better management of bone health is crucial for men treated with ARPIs.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 11164-11164
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (7)

G

Grace L. Lu-Yao

Thomas Jefferson University, Philadelphia, PA

S

Scott W. Keith

Division of Biostatistics, Department of Pharmacology & Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA

K

Krupa Gandhi

Division of Biostatistics, Department of Pharmacology & Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA

H

Hushan Yang

Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA

A

Amy L. Shaver

Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA

N

Nikita Nikita

Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA

W

William Kevin Kelly

Thomas Jefferson University Hospital, Philadelphia, PA