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RC48 单药或联合免疫治疗局部晚期或转移性尿路上皮癌的多中心真实世界研究:HER2 靶向抗体偶联药物。

HER2-targeting antibody-drug conjugate RC48 alone or in combination with immunotherapy for locally advanced or metastatic urothelial carcinoma: a multicenter, real-world study.

机构信息

Department of Medical Oncology, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, No. 651, Dongfeng East Road, Yuexiu District, Guangzhou, 510060, China.

Department of Urology, Sun Yat-Sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, No. 651, Dongfeng East Road, Yuexiu District, Guangzhou, 510060, China.

出版信息

Cancer Immunol Immunother. 2023 Jul;72(7):2309-2318. doi: 10.1007/s00262-023-03419-1. Epub 2023 Mar 10.

Abstract

BACKGROUND

Phase II trials showed the efficacy of anti-HER2 RC48-ADC (disitamab vedotin) for HER2-positive metastatic urothelial carcinoma (UC). This study evaluated RC48 alone verses in combination with immunotherapy for locally advanced or metastatic UC using real-world data.

METHODS

This retrospective, multicenter, real-world study included patients with locally advanced or metastatic UC who received RC48 in five hospitals in China between July 2021 and April 2022. The outcomes were progression-free survival (PFS), overall survival (OS), objective response rate (ORR), disease control rate (DCR), and adverse events.

RESULTS

Thirty-six patients were included. The patients were 47-87 years, and 26 (72.2%) were male. Eighteen patients received RC48 alone, and 18 received RC48 combined with a programmed death-1 antibody. The median PFS was 5.4 months. The median OS was not reached. The 6-month and 1-year PFS rates were 38.8% and 15.5%, respectively. The 1-year OS rate was 79.6%. Fourteen (38.9%) patients achieved a partial response, and the ORR was 38.9%. Eleven patients had stable disease, and the DCR was 69.4%. The median PFS for patients who received RC48 combined with immunotherapy and those who received RC48 alone was 8.5 and 5.4 months, respectively. The main treatment-related adverse events included anemia, hypoesthesia, fatigue, and elevated transaminase. No treatment-related death occurred.

CONCLUSION

RC48 alone or combined with immunotherapy might benefit patients with locally advanced or metastatic UC, regardless of impaired renal function.

摘要

背景

Ⅱ期临床试验表明抗 HER2 RC48-ADC(注射用维迪西妥单抗)对 HER2 阳性转移性尿路上皮癌(UC)有效。本研究使用真实世界数据评估了 RC48 单药治疗与联合免疫治疗局部晚期或转移性 UC 的疗效。

方法

这是一项回顾性、多中心、真实世界研究,纳入了 2021 年 7 月至 2022 年 4 月期间在中国五家医院接受 RC48 治疗的局部晚期或转移性 UC 患者。主要研究终点为无进展生存期(PFS)、总生存期(OS)、客观缓解率(ORR)、疾病控制率(DCR)和不良事件。

结果

共纳入 36 例患者,年龄 47-87 岁,男性 26 例(72.2%)。18 例患者接受 RC48 单药治疗,18 例患者接受 RC48 联合 PD-1 抗体治疗。中位 PFS 为 5.4 个月,中位 OS 未达到。6 个月和 1 年的 PFS 率分别为 38.8%和 15.5%,1 年 OS 率为 79.6%。14 例(38.9%)患者获得部分缓解,ORR 为 38.9%。11 例患者疾病稳定,DCR 为 69.4%。接受 RC48 联合免疫治疗和接受 RC48 单药治疗的患者中位 PFS 分别为 8.5 和 5.4 个月。主要治疗相关不良事件包括贫血、感觉迟钝、乏力和转氨酶升高。未发生治疗相关死亡。

结论

RC48 单药或联合免疫治疗可能使局部晚期或转移性 UC 患者获益,无论肾功能是否受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79e0/10992583/12fb4e9e37e5/262_2023_3419_Fig1_HTML.jpg

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