夏媛媛, 张国庆, 胡毅. 非小细胞肺癌患者T790M突变致酪氨酸激酶的耐药机制及用药策略[J]. 解放军医学院学报, 2016, 37(8): 897-900,919. DOI: 10.3969/j.issn.2095-5227.2016.08.021
引用本文: 夏媛媛, 张国庆, 胡毅. 非小细胞肺癌患者T790M突变致酪氨酸激酶的耐药机制及用药策略[J]. 解放军医学院学报, 2016, 37(8): 897-900,919. DOI: 10.3969/j.issn.2095-5227.2016.08.021
XIA Yuanyuan, ZHANG Guoqing, HU Yi. Mechanisms and treatment strategy of T790M-mediated resistance in patients with non-small cell lung cancer[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(8): 897-900,919. DOI: 10.3969/j.issn.2095-5227.2016.08.021
Citation: XIA Yuanyuan, ZHANG Guoqing, HU Yi. Mechanisms and treatment strategy of T790M-mediated resistance in patients with non-small cell lung cancer[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(8): 897-900,919. DOI: 10.3969/j.issn.2095-5227.2016.08.021

非小细胞肺癌患者T790M突变致酪氨酸激酶的耐药机制及用药策略

Mechanisms and treatment strategy of T790M-mediated resistance in patients with non-small cell lung cancer

  • 摘要: 随着分子靶向治疗在非小细胞肺癌(non-small cell lung cancer,NSCLC)治疗中的广泛应用,一线接受表皮生长因子受体酪氨酸激酶抑制剂(epidermal growth factor receptor-tyrosine kinase inhibitor,EGFR-TKI)治疗患者的平均总生存期达到2年。但即使对于EGFR-TKI高度敏感的患者,经过10 ~ 12个月治疗后也会发生EGFR-TKI获得性耐药,而T790M突变是最主要的获得性耐药机制。近年来,针对T790M突变导致的EGFR-TKI获得性耐药的治疗策略不断涌现。本文就NSCLC中T790M基因突变的可能耐药机制、检测方法及耐药后应对策略等方面的最新研究进展进行综述。

     

    Abstract: Recently, with the wide application of molecularly targeted therapy in the treatment of non-small cell lung cancer (NSCLC), the average overall survival time of patients who have undergone first line EGFR-tyrosine kinase inhibitor (TKI) treatment can be up to 2 years. But in the process of treatment, even for patients who are highly sensitive to EGFR TKI, drug resistance will eventually emerge at 10 to 12 months after TKI administration. Studies find that the main mechanism of acquired resistant is the secondary mutation of T790M in exon 20 of EGFR. In recent years, detection techniques for T790M mutation as well as treatment strategies for acquired EGFR-TKI resistance caused by T790M mutation update constantly. In this review, we summarize the latest research development about T790M mutation in terms of its mechanisms involved in EGFR-TKI resistance, advanced detection assays and ongoing strategies against the mutation subtype.

     

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