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辅助纳武利尤单抗治疗高危尿路上皮癌根治术后的疗效和安全性:来自单一机构真实世界数据的初步报告。

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.

机构信息

Department of Genitourinary Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Department of Medical Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

出版信息

Int J Clin Oncol. 2024 Dec;29(12):1925-1930. doi: 10.1007/s10147-024-02619-8. Epub 2024 Sep 12.

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.

摘要

背景

CheckMate 274 三期临床试验表明,在接受根治性手术后的高危尿路上皮癌(UC)患者中,辅助 nivolumab 比安慰剂更具优势。然而,在日本,尚无关于辅助 nivolumab 的疗效和安全性的真实世界数据。

方法

本回顾性研究纳入了 2022 年至 2024 年期间在我院接受根治性手术后接受辅助 nivolumab 治疗的高危 UC 患者。我们根据不良事件常用术语标准,第 5.0 版评估免疫相关不良事件(irAE)。Kaplan-Meier 曲线用于评估无病生存期(DFS)和总生存期(OS)。

结果

确定了 33 例接受根治性手术后辅助 nivolumab 治疗的高危 UC 患者,中位随访时间为 11 个月。3 例患者发生 3 级 irAE,8 例因 irAE 停止辅助 nivolumab 治疗。未观察到 4 级或 5 级 irAE。8 例患者已完成 1 年治疗,9 例正在治疗中。9 例患者复发,1 例死于癌症。9 例复发患者中,6 例在辅助 nivolumab 治疗期间复发,2 例在完成 1 年治疗后复发,1 例在 irAE 停止后复发。1 年和 2 年的 OS 率分别为 100%和 90%,中位 OS 未达到。1 年和 2 年的 DFS 率分别为 70%和 60%,中位 DFS 为 26 个月。

结论

辅助 nivolumab 似乎对日本患者具有一定疗效。由于这是一种术后辅助治疗,需要仔细选择患者。

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