Cancer Discov. 2019 Oct;9(10):OF2. doi: 10.1158/2159-8290.CD-NB2019-101. Epub 2019 Aug 30.
The FDA has approved entrectinib for patients with any solid tumor bearing fusions, making it the second TRK inhibitor to receive a tissue-agnostic approval; larotrectinib was the first. How the drugs compare to each other remains unknown. Entrectinib was also approved to treat metastatic non-small cell lung cancer with rearrangements.
美国食品药品监督管理局(FDA)已批准恩曲替尼用于患有任何携带融合基因的实体瘤患者,使其成为第二种获得不考虑组织类型批准的TRK抑制剂;拉罗替尼是第一种。这两种药物如何相互比较仍不清楚。恩曲替尼还被批准用于治疗具有重排的转移性非小细胞肺癌。