Evaluation of optimal timing and therapeutic efficacy of radium-223 therapy for metastatic castration-resistant prostate cancer: a multicenter collaborative study.

IF 1.9 4区 医学 Q3 ONCOLOGY Japanese journal of clinical oncology Pub Date : 2025-01-17 DOI:10.1093/jjco/hyaf007
Fumihiko Urabe, Soshi Kadena, Kojiro Tashiro, Kenichi Tokuoka, Yuki Taneda, Kensuke Fujiwara, Yuma Goto, Juria Nakano, Shota Kawano, Yuya Iwamoto, Wataru Fukuokaya, Yu Imai, Kosuke Iwatani, Mahito Atsuta, Kagenori Ito, Takafumi Yanagisawa, Masaya Murakami, Shunsuke Tsuzuki, Toshihiro Yamamoto, Tatsuya Shimomura, Jun Miki, Takahiro Kimura
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Abstract

Background: Despite its demonstrated efficacy in prolonging overall survival (OS) and delaying skeletal-related events in the ALSYMPCA trial, the optimal timing of radium-223 initiation remains unclear. This study investigated factors influencing radium-223 treatment outcomes, including completion rates and survival.

Methods: This retrospective, multi-institutional study included 164 patients with metastatic castration-resistant prostate cancer (CRPC) who received radium-223 therapy. The primary endpoint was OS following radium-223 initiation. Secondary endpoints included factors associated with incomplete radium-223 treatment (< six cycles) and poor OS. Multivariate Cox regression and multivariate logistic regression analyses were conducted to identify prognostic factors.

Results: The median OS times after CRPC diagnosis and radium-223 initiation were 39 and 12.5 months, respectively. Kaplan-Meier analysis showed that the OS of patients who completed six cycles of radium-223 treatment was longer than that of those who did not (18 vs. 5 months; P < .001). Multivariate Cox analysis identified Eastern Cooperative Oncology Group performance status (ECOG-PS) ≥ 1 (hazard ratio [HR] = 1.74, P = .046), PSA > 17 ng/ml (HR = 2.93, P < .001), and radium-223 incompletion (HR = 3.23, P < .001) as independent predictors of poor OS. The radium-223 completion rate was 68.3%, and incompletion was significantly associated with prior docetaxel use (odds ratio [OR] = 5.97, P = .001), bone pain (OR = 2.64, P = .024), and PSA > 17 ng/ml at the start of radium-223 treatment (OR = 3.12, P = .013).

Conclusions: Completion of all six cycles of radium-223 treatment were associated with favorable survival outcomes in metastatic CRPC patients. Prior docetaxel use, bone pain, and elevated PSA levels were significant risk factors for radium-223 incompletion. These findings suggest the importance of initiating radium-223 earlier in the treatment course for patients with favorable clinical profiles to maximize the therapeutic benefits.

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评估镭-223治疗转移性去势抵抗性前列腺癌的最佳时机和治疗效果:一项多中心合作研究。
背景:尽管在ALSYMPCA试验中显示出延长总生存期(OS)和延迟骨骼相关事件的功效,但镭-223的最佳起始时间仍不清楚。本研究调查了影响镭223治疗结果的因素,包括完成率和生存率。方法:这项回顾性、多机构研究包括164例接受镭-223治疗的转移性去势抵抗性前列腺癌(CRPC)患者。主要终点是镭-223起始后的OS。次要终点包括与镭-223治疗不完全(< 6个周期)和不良OS相关的因素。采用多因素Cox回归和多因素logistic回归分析确定预后因素。结果:CRPC诊断和镭-223起始治疗后的中位OS时间分别为39个月和12.5个月。Kaplan-Meier分析显示,完成6个周期镭-223治疗的患者的OS长于未完成治疗的患者(18个月vs. 5个月;P = 17 ng/ml (HR = 2.93, 223治疗开始时P = 17 ng/ml (OR = 3.12, P = 0.013)。结论:在转移性CRPC患者中,完成所有六个周期的镭-223治疗与良好的生存结果相关。既往使用多西他赛、骨痛和PSA水平升高是镭-223不完全性的重要危险因素。这些研究结果表明,对于具有良好临床表现的患者,在治疗过程中早期开始镭-223治疗以最大限度地提高治疗效果的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.70
自引率
8.30%
发文量
177
审稿时长
3-8 weeks
期刊介绍: Japanese Journal of Clinical Oncology is a multidisciplinary journal for clinical oncologists which strives to publish high quality manuscripts addressing medical oncology, clinical trials, radiology, surgery, basic research, and palliative care. The journal aims to contribute to the world"s scientific community with special attention to the area of clinical oncology and the Asian region. JJCO publishes various articles types including: ・Original Articles ・Case Reports ・Clinical Trial Notes ・Cancer Genetics Reports ・Epidemiology Notes ・Technical Notes ・Short Communications ・Letters to the Editors ・Solicited Reviews
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