Department of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Department of Thoracic Oncology, Hyogo College of Medicine, Hyogo, Japan.
Oncoimmunology. 2021 Jul 8;10(1):1950411. doi: 10.1080/2162402X.2021.1950411. eCollection 2021.
Although previous studies suggest that cancer cachexia is a poor prognostic factor for immune checkpoint inhibitor monotherapy, the impact of cancer cachexia on chemoimmunotherapy is unclear. We investigated the impact of cancer cachexia on the therapeutic outcomes of chemoimmunotherapy for non-small cell lung cancer (NSCLC). We retrospectively analyzed patients' medical records with NSCLC who received chemoimmunotherapy in 12 institutions in Japan between January and November 2019. We defined cancer cachexia as weight loss exceeding 5% of the total body weight or a body mass index of < 20 kg/m and weight loss of more than 2% of the total body weight within 6 months before chemoimmunotherapy initiation, with laboratory results exceeding reference values. This study enrolled 235 patients with NSCLC, among whom 196 were eligible for analysis, and 50 (25.5%) met the criteria for cachexia diagnosis. Patients with cancer cachexia had a significantly higher frequency of a programmed death-ligand 1 (PD-L1) expression of ≥ 50% (48%, = .01) and shorter progression-free survival (PFS; log-rank test: = .04) than patients without cachexia. There was no significant difference in overall survival (OS) between the cachexia and no-cachexia groups (log-rank test: = .14). In the PD-L1 ≥ 50% population, there was no significant difference in PFS and OS (log-rank test: = .19 and = .79, respectively) between patients with NSCLC in the cachexia or no-cachexia groups. Cancer cachexia might be a poor prognostic factor in patients with NSCLC receiving chemoimmunotherapy.
尽管先前的研究表明癌症恶病质是免疫检查点抑制剂单药治疗的预后不良因素,但癌症恶病质对化疗免疫治疗的影响尚不清楚。我们研究了癌症恶病质对非小细胞肺癌(NSCLC)化疗免疫治疗疗效的影响。我们回顾性分析了 2019 年 1 月至 11 月日本 12 家机构接受化疗免疫治疗的 NSCLC 患者的病历。我们将癌症恶病质定义为体重减轻超过总体重的 5%或 BMI<20kg/m且在化疗免疫治疗开始前 6 个月内体重减轻超过 2%,且实验室结果超过参考值。本研究共纳入 235 例 NSCLC 患者,其中 196 例符合分析条件,50 例(25.5%)符合恶病质诊断标准。有癌症恶病质的患者程序性死亡配体 1(PD-L1)表达≥50%的频率显著更高(48%, =.01),无进展生存期(PFS;对数秩检验: =.04)更短。恶病质组和无恶病质组的总生存期(OS)无显著差异(对数秩检验: =.14)。在 PD-L1≥50%的人群中,恶病质组和无恶病质组的 PFS 和 OS 无显著差异(对数秩检验: =.19 和 =.79)。癌症恶病质可能是接受化疗免疫治疗的 NSCLC 患者的预后不良因素。