首页> 美国卫生研究院文献>other >CMET-30. BRAIN METASTASES FROM EGFR-MUTATED NSCLC WHICH HAD ACQUIRED RESISTANCE TO EGFR-TKI. ~LESS-FREQUENT T790M AND PRESERVED RESPONSE TO OTHER TKIs~
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CMET-30. BRAIN METASTASES FROM EGFR-MUTATED NSCLC WHICH HAD ACQUIRED RESISTANCE TO EGFR-TKI. ~LESS-FREQUENT T790M AND PRESERVED RESPONSE TO OTHER TKIs~

机译:CMET-30。 EGFR突变型NSCLC对EGFR-TKI产生耐药性引起的脑转移。 〜很少的T790M并保留对其他TKI的响应〜

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摘要

BACKGROUNDDespite the favorable response, most brain metastases (MBs) acquire resistance to TKIs. T790M is the most common mechanism and accounts for approximately half of acquired resistance to TKIs. The aim of this study is to clarify the role of T790M in the acquired resistance of BMs, and optimal treatment for BMs progressed after TKI. METHOD: Upfront TKI was performed for BMs from EGFR-mutated NSCLC, and TKI was changed at progression. Gefitinib, erlotinib, afatinib and osimertinib were used and the selection of these TKIs were owing to the physicians’ decision. During the disease course, re-biopsies of progressed diseases were performed to verify mutations of EGFR, and the incidences of T790M were compared among the organs biopsied. The time to CNS-progression (TCP) were evaluated for each TKI.
机译:背景技术尽管反应良好,但大多数脑转移瘤(MB)仍对TKI具有抵抗力。 T790M是最常见的机制,约占获得的对TKI抵抗力的一半。这项研究的目的是阐明T790M在获得性BM抵抗中的作用,以及在TKI后对BM进行最佳治疗的方法。方法:对来自EGFR突变的NSCLC的BM进行前期TKI,并在进展时改变TKI。使用吉非替尼,厄洛替尼,阿法替尼和奥西替尼,而这些TKI的选择取决于医生的决定。在病程中,对进行中的疾病进行活检以验证EGFR突变,并比较活检器官中T790M的发生率。对于每个TKI,评估了CNS进行时间(TCP)。

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