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帕博利珠单抗联合化疗与帕博利珠单抗单药治疗的失败时间比较:高 PD-L1 表达的 NSCLC 患者的连续分析。

Comparison of time to failure of pembrolizumab plus chemotherapy versus pembrolizumab monotherapy: a consecutive analysis of patients having NSCLC with high PD-L1 expression.

机构信息

Department of Thoracic Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

出版信息

Cancer Immunol Immunother. 2022 Mar;71(3):737-746. doi: 10.1007/s00262-021-03029-9. Epub 2021 Aug 14.

Abstract

INTRODUCTION

There are two treatment strategies for non-small cell lung cancer (NSCLC) exhibiting a high expression level of programmed death-ligand 1 (tumor proportion score ≥ 50%): pembrolizumab plus chemotherapy and monotherapy. We retrospectively compared their efficacy and safety.

MATERIALS AND METHODS

We reviewed the efficacy and safety of first-line pembrolizumab-containing regimens administered between 2017 and 2020 to consecutive patients. The patients were divided into a pembrolizumab plus chemotherapy group (Combo group) or monotherapy group (Mono group). To compare the efficacy, we monitored the time to failure of strategy (TFS) defined as the time from the start of treatment to the occurrence of one of the following events: the addition of any drug not included in the primary strategy, progression of cancer after complete therapy, progression and no subsequent therapy, or death, whichever occurred first. We used the propensity score matching (PSM) to reduce the bias.

RESULTS

A total of 126 patients were identified (89 in the Mono group and 37 in the Combo group). PSM matched 36 individuals from each of the two groups. The overall response rate and median progression-free survival of the Combo group were better than those of the Mono group. However, the median TFS was almost the same (11.3 months vs. 14.9 months; hazard ratio 1.40 [95% confidence interval 0.62-3.15]). The frequency of all serious adverse effects was higher in the Combo group than in the Mono group.

DISCUSSION

Due to similar efficacy in TFS, both pembrolizumab plus chemotherapy and monotherapy are valid options for NSCLC.

摘要

简介

对于程序性死亡配体 1(肿瘤比例评分≥50%)表达水平高的非小细胞肺癌(NSCLC),有两种治疗策略:帕博利珠单抗联合化疗和单药治疗。我们回顾性比较了它们的疗效和安全性。

材料和方法

我们回顾了 2017 年至 2020 年间连续接受一线含帕博利珠单抗方案治疗的患者的疗效和安全性。患者被分为帕博利珠单抗联合化疗组(联合组)或单药治疗组(单药组)。为了比较疗效,我们监测了策略失效时间(TFS),定义为从治疗开始到以下任何事件发生的时间:添加任何未包含在初始策略中的药物、完全治疗后癌症进展、进展且无后续治疗或死亡,以先发生者为准。我们使用倾向评分匹配(PSM)来减少偏倚。

结果

共纳入 126 例患者(单药组 89 例,联合组 37 例)。PSM 匹配了每组 36 例患者。联合组的总缓解率和中位无进展生存期优于单药组。然而,中位 TFS 几乎相同(11.3 个月 vs. 14.9 个月;风险比 1.40 [95%置信区间 0.62-3.15])。联合组的所有严重不良事件发生率均高于单药组。

讨论

由于 TFS 疗效相似,帕博利珠单抗联合化疗和单药治疗都是 NSCLC 的有效选择。

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