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阿替利珠单抗治疗既往治疗的局部晚期或转移性尿路上皮膀胱癌患者的真实世界数据。

Real-world data of atezolizumab in patients with previously treated locally advanced or metastatic urothelial bladder cancer.

机构信息

Pharmacy Service, Hospital de Valme. Área de Gestión Sanitaria Sur de Sevilla, Seville, Spain.

Oncology Service, Hospital de Valme. Área de Gestión Sanitaria Sur de Sevilla, Seville, Spain.

出版信息

Int J Clin Pharm. 2024 Apr;46(2):382-389. doi: 10.1007/s11096-023-01667-w. Epub 2023 Dec 19.

Abstract

BACKGROUND

Clinical trials of atezolizumab for locally advanced or metastatic urothelial bladder cancer (mUBC) report controversial efficacy data. Furthermore, real-world evidence about this use is limited.

AIM

We aimed to evaluate the effectiveness of atezolizumab in a real-world population with mUBC, to explore effectiveness with regard to selected poor prognostic criteria such as performance status by Eastern Oncology Cooperative Group (ECOG), hemoglobin levels and liver metastases, and to determine the safety profile of atezolizumab.

METHOD

Multicenter, retrospective real-world study including previously treated mUBC patients who received atezolizumab. The primary endpoint was overall survival (OS). Additionally, progression-free survival (PFS), best response reached and safety data were analyzed. A descriptive analysis was performed, while OS and PFS were estimated by Kaplan-Meier method.

RESULTS

A total of 185 patients (84.9% men, median age 69 years) were included. Median PFS was 4.8 months [95% confidence interval (CI) 3.6-6.0], and median OS was 20.0 months (95% CI 11.8-28.5), with an objective response rate of 28.1%. OS was higher for patients with ECOG 0-1 versus 2-3 [24.5 months (95% CI 14.5-34.6) vs. 5.2 (95% CI 4.4-6.0), p = 0.004]; and for patients without liver metastases [25.4 months (95% CI 16.2-34.6) vs. 6.4 months (95% CI 4.0-8.1), p = 0.006]. Regarding hemoglobin levels, no survival differences were detected. Adverse events were registered in 55.1% of patients.

CONCLUSION

In a real-world population with previously treated mUBC, atezolizumab seems to provide clinically relevant benefit, which is even higher for patients with ECOG 0-1 and without liver metastases, with an acceptable safety profile.

摘要

背景

阿替利珠单抗治疗局部晚期或转移性尿路上皮膀胱癌(mUBC)的临床试验报告了疗效数据存在争议。此外,关于这种用途的真实世界证据有限。

目的

我们旨在评估阿替利珠单抗在 mUBC 真实世界人群中的有效性,探讨其在选择不良预后标准(如东部肿瘤协作组 [ECOG] 表现状态、血红蛋白水平和肝转移)方面的有效性,并确定阿替利珠单抗的安全性特征。

方法

这是一项多中心、回顾性真实世界研究,纳入了先前接受过阿替利珠单抗治疗的 mUBC 患者。主要终点是总生存期(OS)。此外,还分析了无进展生存期(PFS)、最佳缓解情况和安全性数据。采用描述性分析,OS 和 PFS 采用 Kaplan-Meier 法进行估计。

结果

共纳入 185 例患者(84.9%为男性,中位年龄 69 岁)。中位 PFS 为 4.8 个月[95%置信区间(CI)3.6-6.0],中位 OS 为 20.0 个月[95%CI 11.8-28.5],客观缓解率为 28.1%。ECOG 0-1 组患者的 OS 高于 ECOG 2-3 组[24.5 个月(95%CI 14.5-34.6)与 5.2 个月(95%CI 4.4-6.0),p=0.004],无肝转移患者的 OS 高于有肝转移患者[25.4 个月(95%CI 16.2-34.6)与 6.4 个月(95%CI 4.0-8.1),p=0.006]。关于血红蛋白水平,未检测到生存差异。55.1%的患者发生了不良事件。

结论

在先前治疗过的 mUBC 真实世界人群中,阿替利珠单抗似乎提供了有临床意义的获益,ECOG 0-1 且无肝转移的患者获益更高,且安全性可接受。

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