| Literature DB >> 35726802 |
Lorenzo Belluomini1, Alice Avancini1,2, Luca Pasqualin1, Jessica Insolda1, Marco Sposito1, Jessica Menis1, Daniela Tregnago1, Ilaria Trestini1, Miriam Grazia Ferrara3,4, Emilio Bria3,4, Michele Milella1, Sara Pilotto1.
Abstract
INTRODUCTION: Selpercatinib is a RET selective tyrosine kinase inhibitor with nanomolar potency against diverse RET alterations, including fusions, activating point mutations, and acquired resistance mutations. Rearranged during transfection (RET) gene is a validated target in non-small-cell lung cancer (NSCLC). Selpercatinib is currently approved for adult patients with metastatic RET fusion-positive NSCLC. AREAS COVERED: This review summarizes the efficacy and safety data of selpercatinib in the treatment landscape of RET fusion-positive NSCLC. EXPERT OPINION: Globally considered, selpercatinib is an optimal treatment choice, in terms of both (systemic and intracranial) efficacy and safety, in patients affected by advanced NSCLC harboring RET fusions as a driver mechanism. Future challenges include the identification of the most appropriate placement for selpercatinib in the treatment algorithm of RET fusion-positive NSCLC (including early stages), the clarification of resistance mechanisms, as well as of its role in EGFR-mutant NSCLC undergoing progression during osimertinib driven by RET alterations.Entities:
Keywords: Non-small-cell-lung cancer; RET fusion; efficacy; safety; selpercatinib
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Year: 2022 PMID: 35726802 DOI: 10.1080/14737140.2022.2093190
Source DB: PubMed Journal: Expert Rev Anticancer Ther ISSN: 1473-7140 Impact factor: 3.627