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帕博利珠单抗在被认为可能不符合含铂化疗条件的晚期尿路上皮癌患者中的疗效和安全性:KEYNOTE-052和LEAP-011的事后分析

Efficacy and safety of pembrolizumab in patients with advanced urothelial carcinoma deemed potentially ineligible for platinum-containing chemotherapy: Post hoc analysis of KEYNOTE-052 and LEAP-011.

作者信息

O'Donnell Peter H, Loriot Yohann, Csoszi Tibor, Matsubara Nobuaki, Shin Sang Joon, Park Se Hoon, Atduev Vagif, Gumus Mahmut, Karaca Saziye Burcak, Grivas Petros, de Wit Ronald, Castellano Daniel E, Powles Thomas, Vuky Jacqueline, Zhao Yujie, O'Hara Karen, Okpara Chinyere E, Franco Sonia, Homet Moreno Blanca, Żołnierek Jakub, Siefker-Radtke Arlene O

机构信息

Section of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois, USA.

Early Drug Development Department, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

出版信息

Cancer. 2025 Jan 1;131(1):e35601. doi: 10.1002/cncr.35601. Epub 2024 Oct 28.

Abstract

BACKGROUND

First-line pembrolizumab monotherapy is a standard of care for platinum-ineligible patients with advanced urothelial carcinoma (UC). No global standardized definition of platinum ineligibility exists. This study aimed to evaluate the efficacy and safety of pembrolizumab monotherapy in patients with UC who met various criteria for platinum ineligibility.

METHODS

Patients from KEYNOTE-052 and LEAP-011 deemed potentially platinum ineligible were pooled for this post hoc exploratory analysis as follows: group 1: Eastern Cooperative Oncology Group performance status (ECOG PS) 2; group 2: ECOG PS 2 and age ≥80 years, renal dysfunction, or visceral disease; and group 3: any two other factors regardless of ECOG PS. Patients received pembrolizumab 200 mg intravenously every 3 weeks. End points included objective response rate (ORR), progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors, version 1.1, by blinded independent central review, overall survival (OS), and safety.

RESULTS

A total of 612 patients treated with pembrolizumab from KEYNOTE-052 (n = 370) and LEAP-011 (n = 242) were included; the median (range) follow-up was 56.3 months (51.2-65.3 months) and 12.8 months (0.2-25.1 months), respectively. For group 1, ORR was 26.2%, median PFS was 2.7 months, and median OS was 10.1 months. For group 2, ORR ranged from 23.5% to 33.3%, median PFS ranged from 2.1 to 4.4 months, and median OS ranged from 9.1 to 10.1 months. For group 3, ORR ranged from 25.7% to 27.9%, median PFS ranged from 2.1 to 2.8 months, and median OS ranged from 9.0 to 10.6 months. Treatment-related adverse event rates were consistent across groups.

CONCLUSIONS

Frontline pembrolizumab has consistent antitumor activity and safety in patients with advanced UC categorized as potentially ineligible for platinum-based chemotherapy, regardless of the variable definitions of platinum ineligibility used.

摘要

背景

一线帕博利珠单抗单药治疗是铂类药物不适用的晚期尿路上皮癌(UC)患者的标准治疗方案。目前尚无全球统一的铂类药物不适用的标准定义。本研究旨在评估帕博利珠单抗单药治疗符合各种铂类药物不适用标准的UC患者的疗效和安全性。

方法

将KEYNOTE-052和LEAP-011研究中被认为可能不适合使用铂类药物的患者纳入本次事后探索性分析,分组如下:第1组:东部肿瘤协作组体能状态(ECOG PS)为2;第2组:ECOG PS为2且年龄≥80岁、肾功能不全或有内脏疾病;第3组:无论ECOG PS如何,存在任何其他两个因素。患者每3周静脉注射200 mg帕博利珠单抗。终点指标包括客观缓解率(ORR)、根据实体瘤疗效评价标准1.1版由盲法独立中央审查评估的无进展生存期(PFS)、总生存期(OS)和安全性。

结果

共纳入KEYNOTE-052研究(n = 370)和LEAP-011研究(n = 242)中接受帕博利珠单抗治疗的612例患者;中位(范围)随访时间分别为56.3个月(51.2 - 65.3个月)和12.8个月(0.2 - 25.1个月)。第1组的ORR为26.2%,中位PFS为2.7个月,中位OS为10.1个月。第2组的ORR为23.5%至33.3%,中位PFS为2.1至4.4个月,中位OS为9.1至10.1个月。第3组的ORR为25.7%至27.9%,中位PFS为2.1至2.8个月,中位OS为9.0至10.6个月。各治疗组的治疗相关不良事件发生率一致。

结论

对于被归类为可能不适合铂类化疗的晚期UC患者,一线使用帕博利珠单抗具有一致的抗肿瘤活性和安全性,无论所采用的铂类药物不适用的不同定义如何。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b968/11694235/ed87ad99d726/CNCR-131-0-g004.jpg

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