A retrospective study of prognostic factors and prostate-specific antigen dynamics in Japanese patients with metastatic hormone-sensitive prostate cancer who received combined androgen blockade therapy with bicalutamide.

IF 2.4 3区 医学 Q3 ONCOLOGY International Journal of Clinical Oncology Pub Date : 2024-10-01 Epub Date: 2024-08-17 DOI:10.1007/s10147-024-02597-x
Yu Tashiro, Shusuke Akamatsu, Kentaro Ueno, Toshiyuki Kamoto, Naoki Terada, Takuya Hida, Ryoma Kurahashi, Tomomi Kamba, Atsushi Saito, Takumi Lee, Satoshi Morita, Takashi Kobayashi
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Abstract

Background: This retrospective observational study explored the therapeutic potential of combined androgen blockade (CAB) with bicalutamide (Bic-CAB) as an initial treatment for metastatic hormone-sensitive prostate cancer (mHSPC) in Japan.

Methods: The electronic health records of 159 patients with mHSPC from three Japanese institutions who received initial treatment with Bic-CAB between 2007 and 2017 were analyzed. The time to prostate-specific antigen (PSA) progression, duration of Bic-CAB treatment, and overall survival (OS), with various definitions for PSA progression, were assessed. A multivariate Cox proportional hazards model was constructed using clinical parameters to predict time to the end of Bic-CAB treatment and OS.

Results: The median observation period was 46.4 months, and the median age of patients at diagnosis was 71 years. A total of 46.5% patients experienced PSA progression with a median survival duration of 29 months (according to Prostate Cancer Clinical Trials Working Group 3 criteria), and 49.1% patients achieved a PSA nadir < 0.2 ng/mL in a median time of 4.7 months. When stratified by PSA nadir and PSA change, patients at low risk for disease progression with a small PSA change due to low initial PSA had a 5-year OS of 100% and a 10-year OS of 75%. The OS during the observation period was 72.9 months.

Conclusion: These findings highlight the potential effect of Bic-CAB in patients with mHSPC who were at low risk for disease progression. Initial treatment with Bic-CAB and adjusting treatment early based on PSA dynamics may be a reasonable treatment plan for these patients.

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一项关于接受比卡鲁胺联合雄激素阻断疗法的日本转移性激素敏感性前列腺癌患者预后因素和前列腺特异性抗原动态的回顾性研究。
研究背景这项回顾性观察研究探讨了联合雄激素阻断(CAB)与比卡鲁胺(Bic-CAB)作为日本转移性激素敏感性前列腺癌(mHSPC)初始治疗方法的治疗潜力:分析了日本三家医疗机构在2007年至2017年间接受Bic-CAB初始治疗的159名mHSPC患者的电子健康记录。根据PSA进展的不同定义,评估了前列腺特异性抗原(PSA)进展时间、Bic-CAB治疗持续时间和总生存期(OS)。利用临床参数构建了多变量Cox比例危险模型,以预测Bic-CAB治疗结束时间和OS:中位观察期为 46.4 个月,患者确诊时的中位年龄为 71 岁。共有46.5%的患者出现PSA进展,中位生存期为29个月(根据前列腺癌临床试验工作组3标准),49.1%的患者达到PSA低点:这些研究结果凸显了Bic-CAB对疾病进展风险较低的mHSPC患者的潜在疗效。使用 Bic-CAB 进行初始治疗,并根据 PSA 的动态变化及早调整治疗方案,可能是这些患者的合理治疗方案。
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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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