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