Section of Oncology, Department of Medicine, University of Verona School of Medicine and Verona University Hospital Trust, Verona, Italy.
Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Expert Rev Anticancer Ther. 2022 Aug;22(8):785-794. doi: 10.1080/14737140.2022.2093190. Epub 2022 Jun 27.
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.
This review summarizes the efficacy and safety data of selpercatinib in the treatment landscape of RET fusion-positive NSCLC.
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 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.
塞普替尼是一种 RET 选择性酪氨酸激酶抑制剂,对多种 RET 改变具有纳米摩尔效力,包括融合、激活点突变和获得性耐药突变。转染期间重排(RET)基因是在非小细胞肺癌(NSCLC)中的一个已验证的靶点。塞普替尼目前被批准用于转移性 RET 融合阳性 NSCLC 的成年患者。
本文综述了塞普替尼在 RET 融合阳性 NSCLC 治疗领域中的疗效和安全性数据。
从全球范围来看,塞普替尼是一种最佳的治疗选择,无论是在疗效还是安全性方面,都适用于患有 RET 融合作为机制的晚期 NSCLC 患者。未来的挑战包括确定塞普替尼在 RET 融合阳性 NSCLC(包括早期阶段)治疗算法中的最佳位置,阐明耐药机制,以及在奥希替尼驱动的 EGFR 突变 NSCLC 进展期间,由 RET 改变引起时,塞普替尼的作用。