Comparative risk of medication-related osteonecrosis of the jaw and survival outcomes with RANKL inhibitors versus bisphosphonates in metastatic prostate cancer.

F Farzeen Fatma Syed (Charleston Area Medical Center, Charleston, WV) S Saad Javaid (1Charleston Area Medical Center, Charleston, United States) J Jennifer Collins (1Charleston Area Medical Center, Charleston, United States) A Amir Kamran (1Department of Hematology/Oncology, Charleston Area Medical Center, Charleston, WV)

Abstract

60 Background: Bone-modifying agents (BMAs) are standard in metastatic prostate cancer, preventing skeletal complications but risking medication-related osteonecrosis of the jaw (MRONJ). Evidence guiding prostate-specific management remains sparse. We investigated real-world MRONJ risk, systemic outcomes, and bone metabolism with RANKL inhibitors (RANKLi) versus bisphosphonates (BP). Methods: Men with metastatic prostate cancer (TriNetX Global, 2000–2024) receiving RANKLi or BP were propensity-matched 1:1 (n = 10,964) for key clinical and treatment factors, including baseline corticosteroid use, osteoporosis, osteopenia, and vitamin D levels. Primary endpoints included MRONJ incidence and hazard; secondary outcomes included antibiotic use (≤2 years), survival, and metabolic bone indices. Results: RANKL inhibition was associated with a significantly higher MRONJ incidence (1.30% vs 0.64%; OR 2.05, 95% CI 1.35–3.13; HR 1.82, 95% CI 1.18–2.79; both p < 0.01). Antibiotic use within 2 years was greater with RANKLi (38.5% vs 34.1%; p < 0.001). Despite these toxicities, RANKLi conferred superior overall survival (37.4 vs 32.5 months; HR 0.89, 95% CI 0.83–0.95; p < 0.0001) and reduced hypercalcemia (0.21% vs 0.46%; p = 0.0278). Conclusions: RANKL inhibition nearly doubled MRONJ risk compared with bisphosphonates but provided clear survival and metabolic advantages. The absolute MRONJ risk remained low yet clinically meaningful, reinforcing the importance of proactive dental surveillance and multidisciplinary care. These findings highlight a critical therapeutic balance of greater skeletal and survival benefit at the cost of increased MRONJ risk while managing metastatic prostate cancer. Outcomes with RANKL inhibitors versus bisphosphonates. Outcome RANKL Inhibitors Bisphosphonates p-value Effect Estimate (95% CI) Medication-related osteonecrosis of the jaw (MRONJ) 1.30% (71/5,460) 0.64% (35/5,460) 0.0008 OR 2.05 (1.35–3.13); HR 1.82 (1.18–2.79) Antibiotic use (≤2 years) 38.5% 34.1% <0.001 — Median overall survival (months) 37.4 32.5 <0.0001 HR 0.89 (0.83–0.95) Hypercalcemia incidence 0.21% 0.46% 0.0278 —

Article Details

Volume / Issue Vol. 44, Issue 7_suppl
Published March 01, 2026
Pages 60-60
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (4)

F

Farzeen Fatma Syed

Charleston Area Medical Center, Charleston, WV

S

Saad Javaid

1Charleston Area Medical Center, Charleston, United States

J

Jennifer Collins

1Charleston Area Medical Center, Charleston, United States

A

Amir Kamran

1Department of Hematology/Oncology, Charleston Area Medical Center, Charleston, WV