Department of Surgery, Saiseikai Fukuoka General Hospital, Fukuoka, Japan.
Department of Biostatistics, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, Yamaguchi, 755-8505, Japan.
Eur J Med Res. 2022 Aug 23;27(1):157. doi: 10.1186/s40001-022-00789-7.
Recently, several meta-analyses have investigated the association between sex and the efficacy of immune checkpoint inhibitors (ICIs) in non-small-cell lung cancer (NSCLC). However, this issue remains controversial, because the results have been inconsistent. Moreover, the effect of sex on outcomes in patients with NSCLC receiving combination chemoimmunotherapy as a first-line therapy is poorly understood. The aim of this study was to examine the association between sex and outcomes in patients with NSCLC receiving combination chemoimmunotherapy as a first-line therapy.
We searched PubMed and Scopus from database inception to Feb 18, 2022 and performed a systematic review and meta-analysis of randomized and controlled clinical trials investigating ICI+non-ICI vs non-ICI as a first-line therapy in NSCLC. The pooled hazard ratios (HRs) and 95% confidence intervals (CIs) for overall survival (OS) and progression-free survival (PFS) in male and female patients were calculated using common and random-effects models.
We analyzed 5,830 patients, comprising 4,137 (71.0%) males and 1,693 (29.0%) females, from nine randomized clinical trials. The pooled HR (95%CI) for OS comparing ICI+non-ICI vs non-ICI was 0.80 (0.72-0.87) for males and 0.69 (0.54-0.89) for females. The pooled HR (95%CI) for PFS comparing ICI+non-ICI vs non-ICI was 0.60 (0.55-0.66) for males and 0.56 (0.44-0.70) for females.
In patients with NSCLC receiving combination chemoimmunotherapy as a first-line therapy, a greater improvement in OS and PFS was observed in female patients than in male patients.
最近,有几项荟萃分析研究了性别与非小细胞肺癌(NSCLC)中免疫检查点抑制剂(ICI)疗效之间的关系。然而,这个问题仍然存在争议,因为结果不一致。此外,性别对接受一线化疗免疫治疗的 NSCLC 患者结局的影响知之甚少。本研究旨在研究性别与接受一线化疗免疫治疗的 NSCLC 患者结局之间的关系。
我们从数据库建立之初到 2022 年 2 月 18 日在 PubMed 和 Scopus 上进行了搜索,并对研究 ICI+非 ICI 与非 ICI 作为 NSCLC 一线治疗的随机对照临床试验进行了系统评价和荟萃分析。使用固定效应和随机效应模型计算男性和女性患者总生存期(OS)和无进展生存期(PFS)的合并危险比(HR)和 95%置信区间(CI)。
我们分析了来自 9 项随机临床试验的 5830 例患者,包括 4137 例(71.0%)男性和 1693 例(29.0%)女性。比较 ICI+非 ICI 与非 ICI 的 OS 合并 HR(95%CI)为男性 0.80(0.72-0.87),女性 0.69(0.54-0.89)。比较 ICI+非 ICI 与非 ICI 的 PFS 合并 HR(95%CI)为男性 0.60(0.55-0.66),女性 0.56(0.44-0.70)。
在接受一线化疗免疫治疗的 NSCLC 患者中,女性患者的 OS 和 PFS 改善较男性患者更为显著。