Efficacy and safety of adjuvant nivolumab after radical surgery for high-risk urothelial carcinoma: a preliminary report of real-world data from a single institution

IF 2.4 3区 医学 Q3 ONCOLOGY International Journal of Clinical Oncology Pub Date : 2024-09-12 DOI:10.1007/s10147-024-02619-8
Yosuke Yasuda, Noboru Numao, Tetsuya Urasaki, Ryosuke Oki, Tomohiko Oguchi, Ryo Fujiwara, Yusuke Yoneoka, Kosuke Takemura, Junji Yonese, Takeshi Yuasa
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Abstract

Background

The phase 3 CheckMate 274 trial demonstrated superiority of adjuvant nivolumab over placebo after radical surgery in patients with high-risk urothelial carcinoma (UC). However, real-world data on the efficacy and safety profile of adjuvant nivolumab in Japan have not been reported.

Methods

This retrospective study enrolled patients with high-risk UC who received adjuvant nivolumab therapy following radical surgery between 2022 and 2024 at our institution. We evaluated immune-related adverse events (irAEs) according to the Common Terminology Criteria for Adverse Events, version 5.0. Kaplan–Meier curves were used to assess disease-free survival (DFS) and overall survival (OS).

Results

Thirty-three patients with high-risk UC receiving adjuvant nivolumab therapy following radical surgery were identified, and median follow-up was 11 months. Three patients experienced grade 3 irAEs, and 8 discontinued adjuvant nivolumab therapy due to irAEs. No grade 4 or 5 irAEs were observed. Eight patients have completed 1 year of treatment, and nine are currently on treatment. Nine patients had recurrences and one died of cancer. Of the nine patients with recurrences, six relapsed while on adjuvant nivolumab therapy, two relapsed after completing 1 year of treatment, and one relapsed after discontinuation of irAE. The 1- and 2-year OS rates were 100% and 90%, respectively, and median OS was not reached. The 1- and 2-year DFS rates were 70% and 60%, respectively, and median DFS was 26 months.

Conclusions

Adjuvant nivolumab appears to have some efficacy in Japanese patients. Since this is a postoperative adjuvant therapy, careful patient selection is warranted.

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高危尿路上皮癌根治术后辅助使用 nivolumab 的有效性和安全性:来自一家机构的真实世界数据初步报告
背景3期CheckMate 274试验显示,在高危尿路上皮癌(UC)患者根治术后,尼妥珠单抗的辅助治疗效果优于安慰剂。本回顾性研究招募了 2022 年至 2024 年期间在我院接受根治术后辅助 nivolumab 治疗的高危 UC 患者。我们根据《不良事件通用术语标准》5.0版评估了免疫相关不良事件(irAEs)。结果33例高风险UC患者在根治术后接受了nivolumab辅助治疗,中位随访时间为11个月。3名患者出现了3级虹膜不良反应,8名患者因虹膜不良反应停止了nivolumab辅助治疗。未观察到4级或5级虹膜不良反应。8名患者已完成1年治疗,9名患者目前仍在接受治疗。9名患者复发,1名患者死于癌症。在9名复发患者中,6人在接受nivolumab辅助治疗期间复发,2人在完成1年治疗后复发,1人在停用irAE后复发。1年和2年的OS率分别为100%和90%,未达到中位OS。1年和2年的DFS率分别为70%和60%,中位DFS为26个月。由于这是一种术后辅助疗法,因此需要谨慎选择患者。
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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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