IUC24429-86 Real-world use of bone-modifying agents (BMA) in patients with metastatic castration-resistant prostate cancer (mCRPC) in the United States

Abstract Background Most patients with prostate cancer experience symptomatic skeletal events, leading to increased morbidity and mortality. BMAs have been approved since 2007 and recommended in mCRPC to prevent SSEs in patients with bone metastases or high-risk of osteoporotic fracture. Herein, we sought to assess real-world trends of BMA administration in patients with mCRPC. Methods We used the de-identified nationwide Flatiron Health electronic health record-derived database to extract patient-level data. Eligibility: patients with mCRPC with available date of mCRPC diagnosis and information on receipt of BMA. Patients were categorized into 2 cohorts based on BMA receipt. Treatment trends of BMA by year of mCRPC diagnosis were summarized using frequency and percentages. Baseline characteristics at mCRPC diagnosis (age, race-ethnicity, practice type, insurance) were compared using the Wilcoxon rank-sum and chi-squared tests. Results Of 24,105 patients with metastatic prostate cancer, 14,112 with mCRPC were eligible and included. A total of 7,990 (56.6%) received BMA while 6,122 (43.4%) did not. BMA receipt cohort: median age was 75 (IQR 67-81), the majority were White (61%), treated in community practice (87%) and had a commercial health plan (80%). BMA non-receipt cohort: median age was 75 (IQR 68-82), the majority were White (61%), treated in community practice (78%), and had a commercial health plan (76%). Use of BMA decreased over time from 56% in 2013 to 46% in 2024 (Table 1). Conclusions Despite recommendations to use BMAs in patients with mCRPC and bone metastasis or high-risk of fracture, our findings reveal a low utilization rate of BMAs in mCRPC with a notable decline over time. This highlights the need to incorporate BMAs in clinical practice.

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Publication Details

Journal
The Oncologist
Published
2025-08-29
DOI
https://doi.org/10.1093/oncolo/oyaf248.048
Primary Topic
Prostate Cancer Treatment and Research
Type
article
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article

IUC24429-86 Real-world use of bone-modifying agents (BMA) in patients with metastatic castration-resistant prostate cancer (mCRPC) in the United States

Emmanuel S. Antonarakis, Y. Jo, Umang Swami, Zeynep İrem Özay et al.
The Oncologist
Prostate Cancer Treatment and Research
article

IUC24429-86 Real-world use of bone-modifying agents (BMA) in patients with metastatic castration-resistant prostate cancer (mCRPC) in the United States

Emmanuel S. Antonarakis, Y. Jo, Umang Swami, Zeynep İrem Özay, Rolf Graf, Rana R. McKay, Soumyajit Roy, Neeraj Agarwal, Marek Ostrowski, N. Sayegh
article en

Abstract

Abstract Background Most patients with prostate cancer experience symptomatic skeletal events, leading to increased morbidity and mortality. BMAs have been approved since 2007 and recommended in mCRPC to prevent SSEs in patients with bone metastases or high-risk of osteoporotic fracture. Herein, we sought to assess real-world trends of BMA administration in patients with mCRPC. Methods We used the de-identified nationwide Flatiron Health electronic health record-derived database to extract patient-level data. Eligibility: patients with mCRPC with available date of mCRPC diagnosis and information on receipt of BMA. Patients were categorized into 2 cohorts based on BMA receipt. Treatment trends of BMA by year of mCRPC diagnosis were summarized using frequency and percentages. Baseline characteristics at mCRPC diagnosis (age, race-ethnicity, practice type, insurance) were compared using the Wilcoxon rank-sum and chi-squared tests. Results Of 24,105 patients with metastatic prostate cancer, 14,112 with mCRPC were eligible and included. A total of 7,990 (56.6%) received BMA while 6,122 (43.4%) did not. BMA receipt cohort: median age was 75 (IQR 67-81), the majority were White (61%), treated in community practice (87%) and had a commercial health plan (80%). BMA non-receipt cohort: median age was 75 (IQR 68-82), the majority were White (61%), treated in community practice (78%), and had a commercial health plan (76%). Use of BMA decreased over time from 56% in 2013 to 46% in 2024 (Table 1). Conclusions Despite recommendations to use BMAs in patients with mCRPC and bone metastasis or high-risk of fracture, our findings reveal a low utilization rate of BMAs in mCRPC with a notable decline over time. This highlights the need to incorporate BMAs in clinical practice.

The OncologistVol. 30(Supplement_1)
The University of Texas MD Anderson Cancer Center (US), Huntsman (United States) (US), University of Minnesota System (US), UC San Diego Health System (US), Huntsman Cancer Institute (US), Emergency Medicine Foundation (US), 1675 Foundation (US), MD Anderson Cancer Center Madrid (ES)
Openalex Percentile: Top 67%
Prostate Cancer Treatment and Research
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