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免疫检查点抑制剂治疗EGFR突变非小细胞肺癌的研究进展

In recent years, epidermal growth factor receptor tyrosine kinase inhibitors have been recommended by many guidelines as first-line drugs for advanced non-small cell lung cancer (NSCLC) with EGFR gene mutations and no resistance. However, with the prolongation of medication time, most appear acquire...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105349/
https://www.ncbi.nlm.nih.gov/pubmed/30172273
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.08.11
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collection PubMed
description In recent years, epidermal growth factor receptor tyrosine kinase inhibitors have been recommended by many guidelines as first-line drugs for advanced non-small cell lung cancer (NSCLC) with EGFR gene mutations and no resistance. However, with the prolongation of medication time, most appear acquired resistance. In recent years, breakthroughs in inhibitors of programmed death-1 (PD-1) and its ligand (PD1 ligand, PD-L1) have rapidly changed the therapeutic model of NSCLC. Recent studies have shown that the efficacy of immune checkpoint inhibitors in EGFR-mutant NSCLC patients is not satisfactory, which might be caused by low PD-L1 expression, inhibitory immune microenvironment and low tumor mutation load. This review will elaborate the immune microenvironment of NSCLC patients with EGFR mutation, the latest study progression of immune checkpoint inhibitors and its combined with TKI, expecting to bring new hopes for the treatment of EGFR-mutant NSCLC patients.
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spelling pubmed-61053492018-08-27 免疫检查点抑制剂治疗EGFR突变非小细胞肺癌的研究进展 Zhongguo Fei Ai Za Zhi 综述 In recent years, epidermal growth factor receptor tyrosine kinase inhibitors have been recommended by many guidelines as first-line drugs for advanced non-small cell lung cancer (NSCLC) with EGFR gene mutations and no resistance. However, with the prolongation of medication time, most appear acquired resistance. In recent years, breakthroughs in inhibitors of programmed death-1 (PD-1) and its ligand (PD1 ligand, PD-L1) have rapidly changed the therapeutic model of NSCLC. Recent studies have shown that the efficacy of immune checkpoint inhibitors in EGFR-mutant NSCLC patients is not satisfactory, which might be caused by low PD-L1 expression, inhibitory immune microenvironment and low tumor mutation load. This review will elaborate the immune microenvironment of NSCLC patients with EGFR mutation, the latest study progression of immune checkpoint inhibitors and its combined with TKI, expecting to bring new hopes for the treatment of EGFR-mutant NSCLC patients. 中国肺癌杂志编辑部 2018-08-20 /pmc/articles/PMC6105349/ /pubmed/30172273 http://dx.doi.org/10.3779/j.issn.1009-3419.2018.08.11 Text en 版权所有©《中国肺癌杂志》编辑部2018 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 综述
免疫检查点抑制剂治疗EGFR突变非小细胞肺癌的研究进展
title 免疫检查点抑制剂治疗EGFR突变非小细胞肺癌的研究进展
title_full 免疫检查点抑制剂治疗EGFR突变非小细胞肺癌的研究进展
title_fullStr 免疫检查点抑制剂治疗EGFR突变非小细胞肺癌的研究进展
title_full_unstemmed 免疫检查点抑制剂治疗EGFR突变非小细胞肺癌的研究进展
title_short 免疫检查点抑制剂治疗EGFR突变非小细胞肺癌的研究进展
title_sort 免疫检查点抑制剂治疗egfr突变非小细胞肺癌的研究进展
topic 综述
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105349/
https://www.ncbi.nlm.nih.gov/pubmed/30172273
http://dx.doi.org/10.3779/j.issn.1009-3419.2018.08.11
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