医学
甲状腺髓样癌
甲状腺癌
癌症研究
肺癌
癌症
肿瘤科
凡德他尼
甲状腺乳突癌
内科学
酪氨酸激酶
受体
作者
Dat Tan Le,Kunapareddy Bhavana
标识
DOI:10.1080/14737140.2023.2267754
摘要
The rearranged during transfection (RET) mutation is an oncogene driver for the development of cancer. Selpercatinib is a highly selective RET inhibitor that has demonstrated anti-tumor activity in RET-mutated cancers. Selpercatinib is approved for use in RET fusion-positive non-small-cell lung cancer (NSCLC), RET-mutated medullary thyroid cancer, RET fusion-positive thyroid cancer, and RET fusion-positive solid tumors.This review summarizes the pharmacology, efficacy, safety, and resistance mechanism of selpercatinib.Selpercatinib has demonstrated durable responses with a favorable safety profile making it an excellent treatment option for RET-mutated cancers. Clinical trials are currently underway to determine the optimal sequencing of selpercatinib in RET fusion-positive lung and RET-mutated medullary thyroid cancer in the first-line setting compared to the current standard of care. Selpercatinib has shown promising anti-tumor activity in various RET-altered solid tumors opening a new treatment option for these patients.
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