FRESCO-2:一项全球性 III 期研究,旨在评估 fruquintinib 治疗转移性结直肠癌的疗效和安全性。

FRESCO-2: a global Phase III study investigating the efficacy and safety of fruquintinib in metastatic colorectal cancer.

机构信息

Department of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 426, Houston, TX 77030, USA.

Ospedale Policlinico San Martino - IRCCS, Largo R. Benzi n.10, Ospedale Policlinico San Martino, Padiglione ex Microbiologia, Piano Terra Levante, 16132, Genova, Italy.

出版信息

Future Oncol. 2021 Aug;17(24):3151-3162. doi: 10.2217/fon-2021-0202. Epub 2021 May 17.

Abstract

Fruquintinib, a novel, highly selective, small-molecule tyrosine kinase inhibitor of VEGF receptors (VEGFRs)-1, -2 and -3, is approved in China for the treatment of metastatic colorectal cancer. FRESCO-2, a global, randomized, double-blind, placebo-controlled, Phase III study, is investigating the efficacy and safety of fruquintinib in patients with refractory metastatic colorectal cancer. Key inclusion criteria include: progression on or intolerance to TAS-102 and/or regorafenib; and prior treatment with approved chemotherapy, anti-VEGF therapy, and, if wild-type, anti-EGFR therapy. Approximately 687 patients will be randomized 2:1 to fruquintinib plus best supportive care or placebo plus best supportive care. Primary and key secondary end points are overall survival and progression-free survival, respectively. FRESCO-2 is enrolling in the USA, Europe, Australia and Japan.

摘要

呋喹替尼是一种新型、高度选择性的小分子血管内皮生长因子受体(VEGFR)-1、-2 和 -3 酪氨酸激酶抑制剂,在中国被批准用于转移性结直肠癌的治疗。FRESCO-2 是一项全球性、随机、双盲、安慰剂对照的 III 期研究,旨在评估呋喹替尼在难治性转移性结直肠癌患者中的疗效和安全性。主要纳入标准包括:对 TAS-102 和/或regorafenib 不耐受或进展;既往接受过批准的化疗、抗 VEGF 治疗,如果为野生型,还接受过抗 EGFR 治疗。约 687 名患者将以 2:1 的比例随机分组,分别接受呋喹替尼联合最佳支持治疗或安慰剂联合最佳支持治疗。主要终点和关键次要终点分别为总生存期和无进展生存期。FRESCO-2 正在美国、欧洲、澳大利亚和日本招募患者。

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