Wu Kan, Xia Bing, Zhang Jing, Li Xin, Yang Shaoyu, Zhang Minna, Zhu Lucheng, Wang Bing, Xu Xiao, Ma Shenglin, Chen Xueqin
Department of Thoracic Oncology, Affiliated Hangzhou Cancer Hospital, Zhejiang University School of Medicine, Hangzhou 310002, China.
Department of Thoracic Oncology, The Forth School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou 310053, China.
Cancers (Basel). 2022 Jul 22;14(15):3568. doi: 10.3390/cancers14153568.
Immune checkpoint inhibitors (ICIs) therapy has revolutionized the treatment patterns of non-small cell lung cancer (NSCLC). However, patients treated with ICIs may experience immune-related adverse events (irAEs). Markers that could predict the onset of irAEs are still unclear. Here, we report the possible correlation of baseline peripheral lymphocytes with irAEs and clinical outcomes in advanced NSCLC patients receiving ICIs. A total of 109 advanced NSCLC patients treated with ICIs from April 2017 to January 2021 were analyzed retrospectively. Logistic and Cox regression analyses was applied to evaluate independent risk factors for irAEs, progression-free survival (PFS), and overall survival (OS). Among these patients, 55 (50.5%) patients experienced irAEs. The level of CD8+ T lymphocytes at baseline was the independent risk factor for the onset of irAEs (p = 0.008). A higher level of CD8+ T lymphocytes was associated with longer PFS (11.0 months vs. 3.0 months, p < 0.001) and OS (27.9 months vs. 11.7 months, p = 0.014). Furthermore, patients who had higher baseline CD8+ T lymphocytes and experienced irAEs had a longer PFS (18.4 months vs. 2.2 months, p < 0.001) and OS (32.8 months vs. 9.0 months, p = 0.001) than those who had lower CD8+ T lymphocytes and no irAEs. Our study highlights the value of baseline peripheral CD8+ T lymphocytes as a predictive factor for irAEs in advanced NSCLC patients receiving ICIs. In addition, patients who have higher baseline CD8+ T lymphocytes and experience irAEs would have a superior PFS and OS.
免疫检查点抑制剂(ICI)疗法彻底改变了非小细胞肺癌(NSCLC)的治疗模式。然而,接受ICI治疗的患者可能会经历免疫相关不良事件(irAE)。能够预测irAE发生的标志物仍不明确。在此,我们报告了晚期NSCLC患者接受ICI治疗时基线外周淋巴细胞与irAE及临床结局之间的可能相关性。对2017年4月至2021年1月期间接受ICI治疗的109例晚期NSCLC患者进行了回顾性分析。应用逻辑回归和Cox回归分析来评估irAE、无进展生存期(PFS)和总生存期(OS)的独立危险因素。在这些患者中,55例(50.5%)经历了irAE。基线CD8 + T淋巴细胞水平是irAE发生的独立危险因素(p = 0.008)。较高水平的CD8 + T淋巴细胞与更长的PFS(11.0个月对3.0个月,p < 0.001)和OS(27.9个月对11.7个月,p = 0.014)相关。此外,基线CD8 + T淋巴细胞水平较高且经历irAE的患者,其PFS(18.4个月对2.2个月,p < 0.001)和OS(32.8个月对9.0个月,p = 0.001)比基线CD8 + T淋巴细胞水平较低且未经历irAE的患者更长。我们的研究强调了基线外周CD8 + T淋巴细胞作为晚期NSCLC患者接受ICI治疗时irAE预测因子的价值。此外,基线CD8 + T淋巴细胞水平较高且经历irAE的患者将具有更好的PFS和OS。