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帕博利珠单抗作为顺铂不耐受的晚期尿路上皮癌的一线治疗(KEYNOTE-052):按年龄和体能状态划分的老年患者的结局。

Pembrolizumab as First-line Therapy in Cisplatin-ineligible Advanced Urothelial Cancer (KEYNOTE-052): Outcomes in Older Patients by Age and Performance Status.

机构信息

University of Washington, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, Seattle, WA, USA.

Fox Chase Cancer Center, Philadelphia, PA, USA.

出版信息

Eur Urol Oncol. 2020 Jun;3(3):351-359. doi: 10.1016/j.euo.2020.02.009. Epub 2020 May 16.

Abstract

BACKGROUND

Patients with treatment-naive advanced urothelial cancer (UC) ineligible for cisplatin-based chemotherapy are typically older and have comorbidities, representing a difficult-to-treat population.

OBJECTIVE

To evaluate the safety and antitumor activity of first-line pembrolizumab in subgroups of cisplatin-ineligible older patients (aged ≥65 and ≥75 yr) with advanced UC in KEYNOTE-052 (NCT02335424), including those with poor performance status (Eastern Cooperative Oncology Group performance status score 2 [ECOG PS2]).

DESIGN, SETTING, AND PARTICIPANTS: Patients were cisplatin ineligible, had treatment-naive, histologically/cytologically confirmed, locally advanced/metastatic UC with measurable disease (Response Evaluation Criteria in Solid Tumors version 1.1 [RECIST v1.1]), and had ECOG PS0-2. Patient subgroups analyzed were aged ≥65yr (n = 302), ≥75 yr (n = 179), ≥65yr with ECOG PS2 (≥65yr+ECOG PS2; n = 119), and ≥75 yr+ECOG PS2 (n = 78).

INTERVENTION

All patients received pembrolizumab 200mg intravenously every 3 wk until confirmed progression, intolerable toxicity, patient withdrawal, or 24 mo of therapy.

OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS

The primary endpoint was objective response rate (ORR) as per RECIST v1.1. The key secondary endpoints were overall survival (OS), duration of response (DOR), and safety.

RESULTS AND LIMITATIONS

ORRs for the ≥65yr, ≥75 yr, ≥65yr+ECOG PS2, and ≥75 yr+ECOG PS2 subgroups were 29%, 27%, 29%, and 31%, respectively; rates of complete and partial responses were similar across subgroups (9%, 5%, 6%, and 6%, and 20%, 22%, 23%, and 24%, respectively). Median DOR and OS were also consistent across the ≥65yr and ≥65yr+ECOG PS2 subgroups and the ≥75 yr and ≥75 yr+ECOG PS2 subgroups. Study limitations included open-label design, lack of a comparator group, and nature of post hoc exploratory analysis.

CONCLUSIONS

The clinical benefit of pembrolizumab in advanced UC appeared to be consistent regardless of age and/or poor performance status.

PATIENT SUMMARY

This study looked at whether older age and poorer performance status affect how well patients with previously untreated advanced urothelial cancer ineligible for standard-of-care treatment respond to pembrolizumab. Outcomes with pembrolizumab were not affected by older age or poorer performance status, making it an effective option.

摘要

背景

不适合顺铂为基础化疗的初治晚期尿路上皮癌(UC)患者通常年龄较大且合并症较多,属于治疗难度较大的人群。

目的

评估帕博利珠单抗在 KEYNOTE-052 (NCT02335424)中不适合顺铂的老年(≥65 岁和≥75 岁)初治晚期 UC 患者亚组中的安全性和抗肿瘤活性,包括体能状态较差(东部肿瘤协作组体能状态评分 2 [ECOG PS2])的患者。

设计、地点和参与者:患者不适合顺铂治疗,患有组织学/细胞学证实的局部晚期/转移性 UC,且有可测量的疾病(实体瘤反应评价标准 1.1 版 [RECIST v1.1]),ECOG PS0-2。分析的亚组为年龄≥65 岁(n=302)、≥75 岁(n=179)、年龄≥65 岁且 ECOG PS2(≥65 岁+ECOG PS2;n=119)、以及年龄≥75 岁且 ECOG PS2(n=78)。

干预

所有患者均接受帕博利珠单抗 200mg 静脉输注,每 3 周 1 次,直至确认疾病进展、不可耐受的毒性、患者退出或治疗 24 个月。

结果和局限性

主要终点为 RECIST v1.1 确认的客观缓解率(ORR)。关键次要终点包括总生存期(OS)、缓解持续时间(DOR)和安全性。

结果

≥65 岁、≥75 岁、≥65 岁+ECOG PS2 和≥75 岁+ECOG PS2 亚组的 ORR 分别为 29%、27%、29%和 31%;完全缓解和部分缓解率在各亚组间相似(9%、5%、6%和 6%,以及 20%、22%、23%和 24%)。中位 DOR 和 OS 在≥65 岁和≥65 岁+ECOG PS2 亚组以及≥75 岁和≥75 岁+ECOG PS2 亚组间也一致。研究的局限性包括开放性设计、缺乏对照组以及是事后探索性分析。

结论

帕博利珠单抗在晚期 UC 中的临床获益似乎不受年龄和/或体能状态的影响。

患者总结

本研究旨在探讨初治晚期尿路上皮癌患者,在不适合标准治疗时,年龄较大和体能状态较差是否会影响其对帕博利珠单抗的反应。帕博利珠单抗的疗效不受年龄或体能状态的影响,是一种有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3c0/8246631/7b60c141b223/nihms-1710683-f0001.jpg

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