Sun Yajun, Zhai Changyun, Chen Xiaoxia, Dong Zhengwei, Hou Likun, Zhou Caicun, Jiang Tao
Department of Medical Oncology, The Sixth People's Hospital of Nantong, Nantong 226011, China.
Department of Medical Oncology, Yancheng TCM Hospital Affiliated to Nanjing University of Chinese Medicine, Yancheng 224001, China.
Transl Lung Cancer Res. 2019 Dec;8(6):748-759. doi: 10.21037/tlcr.2019.10.09.
This study aimed to characterize programmed death ligand-1 (PD-L1) expression and CD8 tumor-infiltrating lymphocytes (TILs) density, and their impact on survival in patients with surgically resected small-cell lung cancer (SCLC).
Fifty-six patients with surgically resected SCLC were included. PD-L1 protein expression and CD8 TILs were tested by immunohistochemistry. A meta-analysis of 15 articles with 1,505 patients that investigated the prevalence and prognostic significance of PD-L1 expression in SCLC was conducted.
Twenty-two (39.3%) patients had positive PD-L1 protein expression and 42 (75.0%) had high CD8 TILs density. PD-L1 expression level was not associated with CD8 TILs density (P=0.528). No any association between clinicopathological features and PD-L1 expression level or CD8 TILs density was observed. Positive PD-L1 expression [hazard ratio (HR) =0.374, P=0.002] and high CD8 TILs density (HR =0.429, P=0.008) were independently associated with significantly longer overall survival (OS), which remain the statistical significance in multivariate analyses (P=0.007, P=0.002; respectively). Meta-analysis showed that the prevalence of positive PD-L1 expression was 0.35 [95% confidence interval (CI), 0.22-0.48] and positive PD-L1 expression was correlated with markedly longer OS (HR =0.61; 95% CI, 0.31-0.91) in patients with SCLC.
The prevalence of PD-L1 expression in surgically resected SCLC is lower than that published for NSCLC. There was no association between PD-L1 expression or CD8 TILs density and clinicopathological parameters. PD-L1 expression and CD8 TILs density was independently correlated with better outcome in patients with SCLC.
本研究旨在描述程序性死亡配体1(PD-L1)的表达情况及CD8肿瘤浸润淋巴细胞(TILs)密度,并探讨其对手术切除的小细胞肺癌(SCLC)患者生存的影响。
纳入56例接受手术切除的SCLC患者。采用免疫组织化学法检测PD-L1蛋白表达和CD8 TILs。对15篇涉及1505例患者的文章进行荟萃分析,以研究SCLC中PD-L1表达的发生率及其预后意义。
22例(39.3%)患者PD-L1蛋白表达呈阳性,42例(75.0%)患者CD8 TILs密度较高。PD-L1表达水平与CD8 TILs密度无关(P = 0.528)。未观察到临床病理特征与PD-L1表达水平或CD8 TILs密度之间存在任何关联。PD-L1表达阳性[风险比(HR)= 0.374,P = 0.002]和CD8 TILs密度较高(HR = 0.429,P = 0.008)与总生存期(OS)显著延长独立相关,在多因素分析中仍具有统计学意义(分别为P = 0.007,P = 0.002)。荟萃分析显示,SCLC患者中PD-L1表达阳性的发生率为0.35[95%置信区间(CI),0.22 - 0.48],且PD-L1表达阳性与明显更长的OS相关(HR = 0.61;95% CI,0.31 - 0.91)。
手术切除的SCLC中PD-L1表达的发生率低于非小细胞肺癌(NSCLC)。PD-L1表达或CD8 TILs密度与临床病理参数之间无关联。PD-L1表达和CD8 TILs密度与SCLC患者的更好预后独立相关。