摘要
近年来,非小细胞肺癌(non-small cell lung cancer,NSCLC)静脉化疗逐渐进入平台期,缓解率(response rate,RR)、平均总生存期(overall survival,OS)无明显改善;随着分子生物学发展,以表皮生长因子受体(epidermal growth factor receptor,EGFR)为靶点的EGFR酪氨酸激酶抑制剂(EGFR-tyrosine kinase inhibitors,EGFRTKIs)在NSCLC的治疗中疗效显著,但患者最终均会出现耐药,关于耐药机制目前尚未完全明确。本文详细报道1例49岁女性EGFR基因19外显子缺失突变肺腺癌患者,在靶向治疗耐药后二次活检发现转化为小细胞肺癌(small cell lung cancer,SCLC),予以SCLC化疗方案两周期有效;通过分析患者诊疗过程、疗效,对相关机制进展作一综述。
In recent years, the chemotherapy of non-small cell lung cancer (NSCLC) has almost been reached a platform stage, and there is no obvious progress in terms of response rate (RR) and overall survival (OS); With the great devel- opment of molecular biology, epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) has good therapeutic effect on the NSCLC. But, almost all patients of EGFR-mutant lung cancers develop drug resistance to these agents. This paper reported a case of a 49-year-old woman with lung adenocarcinoma who had EGFR mutant (19-DEL) treated with EGFR-TKIs. After disease progression, histological examination of a secondary biopsy specimen revealed small cell lung cancer (SCLC) had transformed to SCLC treatment. Through the analysis of the process and effect of her therapy, the following is a summary of the relevant mechanism.
出处
《中国肺癌杂志》
CAS
CSCD
北大核心
2015年第10期656-660,共5页
Chinese Journal of Lung Cancer