Predicting time to castration resistance with androgen-receptor signaling inhibitors in hormone-sensitive prostate cancer: data from ULTRA-Japan Consortium.

IF 2.4 3区 医学 Q3 ONCOLOGY International Journal of Clinical Oncology Pub Date : 2024-10-28 DOI:10.1007/s10147-024-02649-2
Taizo Uchimoto, Kengo Iwatsuki, Kazumasa Komura, Wataru Fukuokaya, Takahiro Adachi, Yosuke Hirasawa, Takeshi Hashimoto, Atsuhiko Yoshizawa, Masanobu Saruta, Saizo Fujimoto, Takafumi Minami, Yutaka Yamamoto, Shogo Yamazaki, Tomoaki Takai, Moritoshi Sakamoto, Yuki Nakajima, Kazuki Nishimura, Ryoichi Maenosono, Takuya Tsujino, Ko Nakamura, Tatsuo Fukushima, Kyosuke Nishio, Yuki Yoshikawa, Shutaro Yamamoto, Kosuke Iwatani, Fumihiko Urabe, Keiichiro Mori, Takafumi Yanagisawa, Shunsuke Tsuduki, Kiyoshi Takahara, Teruo Inamoto, Kazutoshi Fujita, Takahiro Kimura, Yoshio Ohno, Ryoichi Shiroki, Haruhito Azuma
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Abstract

Background: Androgen-receptor signaling inhibitors (ARSIs) become the new standard of care for metastatic hormone-sensitive prostate cancer (mHSPC). It is unknown whether time to castration resistance (TTCR), when using the first-line ARSIs, offers predictive value in mHSPC. We sought to assess the clinical outcomes for mHSPC patients treated with first-line ARSIs focusing on the TTCR.

Methods: Data from the ULTRA-Japan study cohort from five academic institutes (496 mHSPC patients) were retrospectively analyzed.

Results: The median overall survival (OS) in the total cohort was 80 months with a median follow-up of 18 months. Of 496 patients, 332 (67%), 82 (16.5%), and 82 (16.5%) were treated with first-line abiraterone acetate + prednisone, enzalutamide, and apalutamide, respectively. During the follow-up, a total of 155 (31%) were diagnosed with mCRPC with a median TTCR of 10 months. In those 155 patients, TTCR > 12 months is an independent predictor of longer OS from the first-line ARSIs. Cox regression analysis of the TTCR from initiating first-line ARSI in 496 mHSPC patients revealed three variables as independent predictors of shorter TTCR, including Gleason's score (GS) ≥ 9, the extent of disease (EOD) ≥ 2, and the presence of liver metastasis.

Conclusion: Our results indicate that mHSPC patients with those three features are likely to have primary resistance to first-line ARSIs (doublet therapy), thus requiring consideration of other options, such as the recent triplet approach.

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预测激素敏感性前列腺癌患者使用雄激素受体信号转导抑制剂产生阉割抵抗的时间:ULTRA-Japan Consortium 的数据。
背景:雄激素受体信号转导抑制剂(ARSIs)已成为治疗转移性激素敏感性前列腺癌(mHSPC)的新标准。在使用一线 ARSIs 时,阉割耐药时间(TTCR)对 mHSPC 是否具有预测价值尚不清楚。我们试图以TTCR为重点,评估接受一线ARSIs治疗的mHSPC患者的临床疗效:方法:回顾性分析来自五所学术机构的ULTRA-Japan研究队列数据(496例mHSPC患者):结果:所有患者的中位总生存期(OS)为80个月,中位随访时间为18个月。496例患者中,332例(67%)、82例(16.5%)和82例(16.5%)分别接受了醋酸阿比特龙+泼尼松、恩扎鲁胺和阿帕鲁胺一线治疗。在随访期间,共有155名患者(31%)被确诊为mCRPC,中位TTCR为10个月。在这155名患者中,TTCR大于12个月是一线ARSIs延长OS的独立预测因素。对496名mHSPC患者开始一线ARSI治疗后的TTCR进行的Cox回归分析显示,有三个变量是TTCR较短的独立预测因素,包括格里森评分(GS)≥9、疾病范围(EOD)≥2和存在肝转移:我们的研究结果表明,具有这三个特征的mHSPC患者很可能对一线ARSIs(双联疗法)产生原发性耐药,因此需要考虑其他方案,如最近的三联疗法。
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
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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