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程序性死亡配体 1(PD-L1)表达是接受培美曲塞维持治疗的晚期肺腺癌患者生存的一个有前途的预测指标。

PD-L1 expression is a promising predictor of survival in patients with advanced lung adenocarcinoma undergoing pemetrexed maintenance therapy.

机构信息

Department of Thoracic Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, 610041, China.

Department of Pathology, West China Hospital, Sichuan University, Chengdu, 610041, China.

出版信息

Sci Rep. 2020 Sep 30;10(1):16150. doi: 10.1038/s41598-020-73013-3.

DOI:10.1038/s41598-020-73013-3
PMID:32999345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7527332/
Abstract

This study aimed to identify potential predictive factors for the survival of advanced lung adenocarcinoma patients undergoing pemetrexed maintenance therapy. 122 advanced lung adenocarcinoma patients who received pemetrexed maintenance therapy were retrospectively analyzed. Kaplan-Meier method with Log-rank test was used for survival analysis. Univariate and multivariate Cox regression were performed to evaluate prognostic factors for overall survival (OS) and progression-free survival (PFS). Bivariate correlation analysis was used for exploratory purpose. For the whole cohort of 122 patients, median PFS was 11.97 months (95% CI 10.611-13.329) and estimated median OS was 45.07 months (95% CI 31.690-58.450). The mPFS of ALK-positive patients was superior to negative patients (18.27 vs. 11.90 months; P  = 0.039). Patients with ECOG PS 0 (14.4 vs. 11.1 months; p = 0.040) and patients with single-organ metastasis (19.0 vs. 11.0 months; p = 0.014) had prolonged median PFS. Compared with the low PD-L1 expression group, PFS of high PD-L1 expression group were improved (13.6 vs. 11.1 months, p = 0.104, at 1% cut-off; 17.5 vs. 11.1 months, p = 0.009, at 10% cut-off; and 27.5 vs. 11.4 months, p = 0.005, at 50% cut-off). No differences were found between EGFR positive and negative patients. PD-L1 expression was an independent prognostic factor for both PFS and OS times (PFS: HR, 0.175; P  = 0.001; OS: HR, 0.107; P  = 0.036). Bivariate correlation showed a significant positive correlation between PD-L1 expression and PFS (correlation coefficient R = 0.485, P  < 0.001). High PD-L1 expression could be a potential effective predictor for favorable survival of advanced lung adenocarcinoma patients undergoing pemetrexed maintenance therapy.

摘要

本研究旨在确定接受培美曲塞维持治疗的晚期肺腺癌患者生存的潜在预测因素。回顾性分析了 122 例接受培美曲塞维持治疗的晚期肺腺癌患者。采用 Kaplan-Meier 法和 Log-rank 检验进行生存分析。采用单因素和多因素 Cox 回归分析评估总生存期(OS)和无进展生存期(PFS)的预后因素。采用双变量相关性分析进行探索性分析。对于整个 122 例患者队列,中位 PFS 为 11.97 个月(95%CI 10.611-13.329),估计中位 OS 为 45.07 个月(95%CI 31.690-58.450)。ALK 阳性患者的 mPFS 优于阴性患者(18.27 与 11.90 个月;P=0.039)。ECOG PS 0 患者(14.4 与 11.1 个月;p=0.040)和单器官转移患者(19.0 与 11.0 个月;p=0.014)的中位 PFS 延长。与低 PD-L1 表达组相比,高 PD-L1 表达组的 PFS 得到改善(13.6 与 11.1 个月,p=0.104,在 1%截定点;17.5 与 11.1 个月,p=0.009,在 10%截定点;27.5 与 11.4 个月,p=0.005,在 50%截定点)。EGFR 阳性和阴性患者之间无差异。PD-L1 表达是 PFS 和 OS 时间的独立预后因素(PFS:HR 0.175;P=0.001;OS:HR 0.107;P=0.036)。双变量相关性显示 PD-L1 表达与 PFS 之间存在显著正相关(相关系数 R=0.485,P<0.001)。高 PD-L1 表达可能是接受培美曲塞维持治疗的晚期肺腺癌患者生存的潜在有效预测因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0569/7527332/141922c2d567/41598_2020_73013_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0569/7527332/e42c9d88eb12/41598_2020_73013_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0569/7527332/5f460b0a472f/41598_2020_73013_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0569/7527332/141922c2d567/41598_2020_73013_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0569/7527332/e42c9d88eb12/41598_2020_73013_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0569/7527332/5f460b0a472f/41598_2020_73013_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0569/7527332/141922c2d567/41598_2020_73013_Fig3_HTML.jpg

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Cisplatin increases PD-L1 expression and optimizes immune check-point blockade in non-small cell lung cancer.顺铂增加非小细胞肺癌中 PD-L1 的表达并优化免疫检查点阻断。
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PD-L1 (B7-H1) Competes with the RNA Exosome to Regulate the DNA Damage Response and Can Be Targeted to Sensitize to Radiation or Chemotherapy.
程序性死亡配体 1(B7-H1)与 RNA 外切体竞争以调节 DNA 损伤反应,并且可以作为靶点以增敏放疗或化疗。
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Genetic, transcriptional and post-translational regulation of the programmed death protein ligand 1 in cancer: biology and clinical correlations.程序性死亡配体 1 在癌症中的遗传、转录和翻译后调控:生物学和临床相关性。
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Pembrolizumab plus Chemotherapy in Metastatic Non-Small-Cell Lung Cancer.帕博利珠单抗联合化疗治疗转移性非小细胞肺癌。
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