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阿替利珠单抗联合放疗用于浸润性膀胱癌的膀胱保留疗法(BPT-ART)——一项开放标签、II期、多中心研究的研究方案

Bladder preservation therapy in combination with atezolizumab and radiation therapy for invasive bladder cancer (BPT-ART) - A study protocol for an open-label, phase II, multicenter study.

作者信息

Sekino Yuta, Ishikawa Hitoshi, Kimura Tomokazu, Kojima Takahiro, Maruo Kazushi, Azuma Haruhito, Yoshida Ken, Kageyama Yukio, Ushijima Hiroki, Tsuzuki Toyonori, Sakurai Hideyuki, Nishiyama Hiroyuki

机构信息

Department of Radiation Oncology, Faculty of Medicine, University of Tsukuba, Japan.

Department of Urology, Faculty of Medicine, University of Tsukuba, Japan.

出版信息

Contemp Clin Trials Commun. 2021 Jan 21;21:100724. doi: 10.1016/j.conctc.2021.100724. eCollection 2021 Mar.

Abstract

Radical cystectomy (RC) is recommended for muscle-invasive bladder cancer (MIBC) or highest-risk non-muscle-invasive bladder cancer (NMIBC). Trimodal therapy (TMT) is the most favorable strategy among bladder preservation therapies (BPT) for patients who are ineligible for or refuse RC. However, referrals for TMT, especially following chemotherapy, are limited by the patient's condition. Therefore, new BPT approaches are needed. Atezolizumab inhibits programmed death-ligand 1, is well-tolerated in patient populations heavily dominated by renal insufficiency, and is expected to have synergistic anti-tumor effects in combination with radiation therapy (RT). Therefore, we have conducted this open-label phase II multicenter study to evaluate the efficacy and safety of RT in combination with atezolizumab for T2-3 MIBC and highest-risk T1 NMIBC patients. This study was initiated in January 2019, and we aimed to enroll a total of 45 patients. The study is registered in the Japan Registry of Clinical Trials (Identifier: RCT2031180060).

摘要

根治性膀胱切除术(RC)推荐用于肌层浸润性膀胱癌(MIBC)或高危非肌层浸润性膀胱癌(NMIBC)。对于不适合或拒绝接受RC的患者,三联疗法(TMT)是膀胱保留疗法(BPT)中最有利的策略。然而,TMT的转诊,尤其是化疗后的转诊,受到患者病情的限制。因此,需要新的BPT方法。阿替利珠单抗可抑制程序性死亡配体1,在肾功能不全占主导的患者群体中耐受性良好,并且预计与放射治疗(RT)联合使用时具有协同抗肿瘤作用。因此,我们开展了这项开放标签的II期多中心研究,以评估RT联合阿替利珠单抗治疗T2-3期MIBC和高危T1期NMIBC患者的疗效和安全性。本研究于2019年1月启动,我们的目标是共招募45名患者。该研究已在日本临床试验注册中心注册(标识符:RCT2031180060)。

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