Lucitanib for the Treatment of HR+/HER2- Metastatic Breast Cancer: Results from the Multicohort Phase II FINESSE Study

Lucitanib for the Treatment of HR+/HER2- Metastatic Breast Cancer: Results from the Multicohort Phase II FINESSE Study
复制标题

DOI:
10.1158/1078-0432.ccr-19-1164
复制
发表时间:
2020-01-15
影响因子:
11.5
通讯作者:
Curigliano, Giuseppe
Curigliano, Giuseppe
中科院分区:
医学1区
文献类型:
--
作者:
Hui, Rina;Pearson, Alex;Curigliano, Giuseppe

文献摘要

被引文献

相似文献

目的:FGFRI基因在14%的HR+/HER 2(-)乳腺癌患者中扩增。lucitanib,VEGER 1-3,FGFRI-3和PDGER α/β的抑制剂的疗效和安全性进行了评估。患者和方法:HR+/HER 2(-)转移性乳腺癌(MSC)的患者接受口服lucitanib在三个中心确认的队列:(i)FGFR 1扩增,(ii)FGFRI非扩增,11 q13扩增,和(中)FGFR 1和11 q13非扩增。关键入选标准包括东部肿瘤协作组体能状态=一线抗癌治疗,但
Purpose: The FGFRI gene is amplified in 14% of patients with HR+/HER2(-) breast cancer. Efficacy and safety of lucitanib, an inhibitor of VEGER 1-3, FGFRI-3, and PDGER alpha/beta, were assessed.Patients and Methods: Patients with HR+/HER2(-) metastatic breast cancer (MSC) received oral lucitanib in three centrally confirmed cohorts: (i) FGFR1 amplified, (ii) FGFRI nonamplified, 11q13 amplified, and (in) FGFR1 and 11q13 nonamplified. Key inclusion criteria included Eastern Cooperative Oncology Group Performance Status = 1 line of anticancer therapy, but