Department of Internal Medicine, College of Medicine, Chungnam National University, Daejeon, South Korea.
Research Institute for Medical Sciences, College of Medicine, Chungnam National University, Daejeon, South Korea.
Thorac Cancer. 2022 Aug;13(16):2346-2354. doi: 10.1111/1759-7714.14568. Epub 2022 Jul 11.
The use of immune checkpoint inhibitors (ICIs) as first-line treatment rather than as second-line treatment makes a big difference in the drug efficacy and progression-free survival. However, the mechanism for this is still not clear. This study aimed to analyze the effects of the rest period between chemotherapy and immunotherapy on the efficacy of ICIs.
This study included 100 patients with advanced NSCLC treated with PD-1/PD-L1 inhibitors at Chungnam National University Hospital (CNUH) between May 2016 and August 2019. The rest period was defined from the last dose of cytotoxic chemotherapy to the first dose of ICIs. We retrospectively reviewed patients' clinical data and blood test records and analyzed lymphocyte subsets using flow cytometry.
The median rest period was 64 days. The long rest period group (≥36 days) showed significantly higher clinical benefits than the short rest period group (<36 days) (69.4% vs. 39.5%, p = 0.003). White blood cell (WBC) count, absolute neutrophil count (ANC), absolute lymphocyte count (ALC), and neutrophil-lymphocyte ratio (NLR) just before chemotherapy were not different between the two groups. However, the blood test after chemotherapy immediately before immunotherapy showed significantly higher ANC and NLR in the short rest period group than in the long rest period group. The frequency of the Th1 subset and PD-1 + CD8 T cells were significantly higher in the long rest period group than in the short rest period group.
Time interval from chemotherapy to immunotherapy may affect immune cell status and efficacy of ICIs.
免疫检查点抑制剂(ICIs)作为一线治疗而非二线治疗,在药物疗效和无进展生存期方面有很大的不同。然而,其机制尚不清楚。本研究旨在分析化疗和免疫治疗之间的间歇期对 ICI 疗效的影响。
本研究纳入了 2016 年 5 月至 2019 年 8 月期间在忠南国立大学医院(CNUH)接受 PD-1/PD-L1 抑制剂治疗的 100 例晚期 NSCLC 患者。间歇期定义为从最后一剂细胞毒性化疗到 ICI 第一剂的时间。我们回顾性分析了患者的临床数据和血液检测记录,并使用流式细胞术分析了淋巴细胞亚群。
中位间歇期为 64 天。长间歇期组(≥36 天)的临床获益明显高于短间歇期组(<36 天)(69.4% vs. 39.5%,p=0.003)。化疗前的白细胞(WBC)计数、绝对中性粒细胞计数(ANC)、绝对淋巴细胞计数(ALC)和中性粒细胞-淋巴细胞比值(NLR)在两组间无差异。然而,化疗后立即进行免疫治疗前的血液检测显示,短间歇期组的 ANC 和 NLR 明显高于长间歇期组。长间歇期组的 Th1 亚群和 PD-1+CD8 T 细胞的频率明显高于短间歇期组。
化疗和免疫治疗之间的时间间隔可能会影响免疫细胞状态和 ICI 的疗效。