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LIBRETTO-432 研究:辅助塞普替尼对比安慰剂用于治疗融合阳性的 IB-IIIA 期非小细胞肺癌。

LIBRETTO-432, a phase III study of adjuvant selpercatinib or placebo in stage IB-IIIA fusion-positive non-small-cell lung cancer.

机构信息

National Cancer Center Hospital East, Kashiwa, Japan.

David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.

出版信息

Future Oncol. 2022 Sep;18(28):3133-3141. doi: 10.2217/fon-2022-0656. Epub 2022 Aug 11.

Abstract

Selpercatinib, a first-in-class, highly selective and potent central nervous system-active RET kinase inhibitor demonstrated clinically meaningful activity with manageable toxicity in pretreated and treatment-naive advanced/metastatic fusion-positive non-small-cell lung cancer (NSCLC). LIBRETTO-432 is a global, randomized, double-blind, phase III trial evaluating selpercatinib versus placebo in stage IB-IIIA, fusion-positive NSCLC, previously treated with definitive surgery or radiation; participants must have undergone available anti-cancer therapy (including chemotherapy or durvalumab) or not be suitable for it, per investigator's discretion. The primary end point is investigator-assessed event-free survival (EFS) in the primary analysis population (stage II-IIIA fusion-positive NSCLC). Key secondary end points include EFS in the overall population, overall survival, and time to distant disease recurrence in the central nervous system.

摘要

塞尔帕替尼是一种首创的、高度选择性和有效的中枢神经系统活性 RET 激酶抑制剂,在预处理和未治疗的晚期/转移性融合阳性非小细胞肺癌(NSCLC)患者中显示出具有临床意义的活性,且毒性可管理。LIBRETTO-432 是一项全球性、随机、双盲、III 期临床试验,评估了塞尔帕替尼与安慰剂在先前接受过根治性手术或放疗的 IB-IIIA 期、融合阳性 NSCLC 中的疗效;根据研究者的判断,参与者必须接受过可用的抗癌治疗(包括化疗或度伐鲁单抗)或不适合该治疗。主要终点是研究者评估的无事件生存期(EFS)在主要分析人群(IIB-IIIA 期融合阳性 NSCLC)。关键次要终点包括总体人群的 EFS、总生存期和中枢神经系统远处疾病复发时间。

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