Jin Liu, Gu Weiling, Li Xueqin, Xie Liang, Wang Linhong, Chen Zhongwen
Department of Control and Prevention of Chronic Non-communicable Diseases, Jiaxing Center for Disease Control and Prevention, Jiaxing, Zhejiang, China.
Office, Jiaxing Center for Disease Control and Prevention, Jiaxing, Zhejiang,China.
Ther Adv Med Oncol. 2020 Sep 29;12:1758835920962362. doi: 10.1177/1758835920962362. eCollection 2020.
The prognostic value of programmed death-ligand 1 (PD-L1) expression in patients with malignant pleural mesothelioma (MPM) has been controversial according to previous investigations. Therefore, we conducted a meta-analysis to assess the potential prognostic significance of PD-L1 expression in MPM.
PubMed, Embase, Web of Science, Scopus, and the Cochrane Library were thoroughly searched for relevant original articles published before 9 April 2020. The pooled hazard ratios (HRs) and 95% confidence intervals (CIs) of overall survival (OS) and progression-free survival (PFS) were calculated. The results of the meta-analysis were verified using The Cancer Genome Atlas (TCGA) dataset.
In total 16 studies were included in our meta-analysis. A high PD-L1 expression was associated with a poor OS (HR = 1.53, 95% CI = 1.28-1.83, < 0.001), but not a grave PFS (HR = 1.07, 95% CI = 0.82-1.39, = 0.643) in MPM. Furthermore, the PD-L1 expression correlated with the sarcomatoid + biphasic type of MPM (odds ratio = 4.32, 95% CI = 2.16-8.64, < 0.001). TCGA data indicated that PD-L1 was a significant prognostic factor for OS (HR = 2.069, 95% CI = 1.136-3.769, = 0.0175), but not for PFS (HR = 1.205, 95% CI = 0.572-2.539, = 0.624), which was in accordance with the results of the meta-analysis.
A high PD-L1 expression is a significant prognostic factor for poor OS of patients with MPM. We therefore suggest that PD-L1 expression levels can be used to predict the clinical outcomes of patients with MPM in the future.
根据以往的研究,程序性死亡配体1(PD-L1)表达在恶性胸膜间皮瘤(MPM)患者中的预后价值一直存在争议。因此,我们进行了一项荟萃分析,以评估PD-L1表达在MPM中的潜在预后意义。
全面检索了PubMed、Embase、Web of Science、Scopus和Cochrane图书馆,查找2020年4月9日前发表的相关原始文章。计算总生存期(OS)和无进展生存期(PFS)的合并风险比(HR)和95%置信区间(CI)。使用癌症基因组图谱(TCGA)数据集验证荟萃分析的结果。
我们的荟萃分析共纳入16项研究。在MPM中,高PD-L1表达与较差的OS相关(HR = 1.53,95%CI = 1.28 - 1.83,P < 0.001),但与严重的PFS无关(HR = 1.07,95%CI = 0.82 - 1.39,P = 0.643)。此外,PD-L1表达与MPM的肉瘤样+双相型相关(优势比 = 4.32,95%CI = 2.16 - 8.64,P < 0.001)。TCGA数据表明,PD-L1是OS的一个显著预后因素(HR = 2.069,95%CI = 1.136 - 3.769,P = 0.0175),但不是PFS的预后因素(HR = 1.205,95%CI = 0.572 - 2.539,P = 0.624),这与荟萃分析的结果一致。
高PD-L1表达是MPM患者OS较差的一个显著预后因素。因此,我们建议未来可将PD-L1表达水平用于预测MPM患者的临床结局。