外显子
表皮生长因子受体
突变
肺癌
血液学
癌症研究
肿瘤科
内科学
突变体
生物
医学
靶向治疗
癌症
遗传学
基因
作者
Wen‐Qian Li,Jiuwei Cui
标识
DOI:10.1007/s00432-020-03296-6
摘要
With the development of antitumor therapies, different treatment methods including monotherapy and combined therapy have achieved clinical efficacy in advanced epidermal growth factor receptor (EGFR) mutant non-small cell lung cancer (NSCLC) patients. Exon 19 deletion (ex19del) and exon 21 L858R mutation are common sensitive subtypes of EGFR mutation. However, potential distinct mechanisms are found from several dimensions including molecular structures, biological behaviors, concomitant mutations, resistance mechanisms and tumor mutation burdens. More evidence indicates the prognostic difference of EGFR subgroups. This review focused on the progress of potential distinct mechanisms and outcomes in clinical trials of advanced NSCLC patients with ex19del or exon 21 L858R mutation.
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