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. 2025 Aug 8.
doi: 10.1007/s10147-025-02846-7. Online ahead of print.

Post-marketing surveillance of radium-223 chloride in Japanese patients with castration-resistant prostate cancer with bone metastasis-final analysis of 3-year extended follow-up focusing on bone fractures

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Post-marketing surveillance of radium-223 chloride in Japanese patients with castration-resistant prostate cancer with bone metastasis-final analysis of 3-year extended follow-up focusing on bone fractures

Naoya Masumori et al. Int J Clin Oncol. .

Abstract

Background: A post-marketing surveillance (PMS) study was conducted in Japan to assess real-world outcomes with radium-223 treatment in men with metastatic castration-resistant prostate cancer (mCRPC). Results from the treatment period showed that radium-223 was generally well tolerated. Follow-up was subsequently extended to 3 years to collect data on fracture events. Results of the extended follow-up are now reported.

Methods: This prospective, non-interventional, multicenter, single-cohort PMS study enrolled men with CRPC and bone metastases treated with radium-223 under clinical practice. Extended follow-up lasted until 3 years after the first administration of radium-223. Data on clinical fractures and survival were collected.

Results: A total of 334 patients were enrolled, with a median follow-up of 15.3 months (range 1-50). The overall incidence proportion of fractures reported as adverse events was 7.76% (95% confidence interval [CI] 5.09-11.25%), with a fracture incidence rate of 5.22 patients [with fracture]/100 person-years (PY). Patients who received bone-modifying agents (BMAs) had a numerically lower incidence of fractures (5.85%; 3.46/100PY vs 9.93%; 7.92/100PY). Median overall survival was 26.32 months (95% CI 21.65-not reached).

Conclusion: Compared with existing reference data, there was no obvious increase in the incidence of clinical fractures in Japanese patients with mCRPC who were treated with radium-223 under clinical practice. As is already well known for androgen deprivation, BMAs may also be useful in reducing bone fracture after radium-223.

Keywords: Bone metastases; Castration-resistant prostate cancer; Japanese patients; Post-marketing surveillance; Radium-223; Real-world data.

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Conflict of interest statement

Declarations. Conflict of interest: NM received honoraria from Janssen, Astellas, Bayer, Ono Pharmaceutical, and Takeda, and research funding from MSD. ST received honoraria from MSD, Eisai, and Ono Pharmaceutical, and research grants from Eisai, Chugai, Bayer, AstraZeneca, BMS, Ono Pharmaceutical, Daiichi-Sankyo, Novartis, Taiho, and MSD. HU received honoraria from Bayer, Janssen, Takeda, Sanofi and AstraZeneca, and research funding from AstraZeneca. TS, KS, YM, MA, and HK are employees of Bayer Yakuhin, Ltd. MH, YK, and SK reported no conflict of interest. Informed consent: This study was conducted in accordance with Japanese Ministerial Ordinance on Good Post-marketing Study Practice, which does not mandate institutional review board approval for each participating center or written informed consent from patients.

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