Division of Hematology and Oncology, Massachusetts General Hospital, Boston, Massachusetts.
Division of Hematology/Oncology, University of California Irvine, Irvine, California.
Clin Cancer Res. 2019 May 15;25(10):2988-2995. doi: 10.1158/1078-0432.CCR-18-1221. Epub 2018 Sep 17.
MAVERICC compared the efficacy and safety of modified leucovorin/5-fluorouracil/oxaliplatin plus bevacizumab (mFOLFOX6-BV) with leucovorin/5-fluorouracil/irinotecan plus bevacizumab (FOLFIRI-BV) in patients with previously untreated metastatic colorectal cancer (mCRC). MAVERICC was a global, randomized, open-label, phase II study. Primary objectives were to assess associations between (i) excision repair cross-complementing 1 (ERCC1) expression with progression-free survival (PFS), and (ii) plasma VEGF A (VEGF-A) with PFS in patients with previously untreated mCRC receiving mFOLFOX6-BV or FOLFIRI-BV. Before randomization, patients were stratified by tumoral ERCC1/β-actin mRNA expression level and region.
Of 376 enrolled patients, 188 each received mFOLFOX6-BV and FOLFIRI-BV. PFS and overall survival (OS) were comparable between FOLFIRI-BV and mFOLFOX6-BV, with numerically higher PFS [HR = 0.79; 95% CI (confidence interval): 0.61-1.01; = 0.06] and OS (HR = 0.76; 95% CI: 0.56-1.04; = 0.09) observed for FOLFIRI-BV. In the high ERCC1 subgroup, PFS and OS were comparable between treatment groups (PFS, HR = 0.84; 95% CI: 0.56-1.26; = 0.40; OS, HR = 0.80; 95% CI: 0.51-1.26; = 0.33). Across treatment groups, high plasma VEGF-A levels (>5.1 pg/mL) were observed with shorter PFS (HR = 1.19; 95% CI: 0.93-1.53; = 0.17) and significantly shorter OS (HR = 1.64; 95% CI: 1.20-2.24; < 0.01) versus low levels (≤5.1 pg/mL). Safety findings for FOLFIRI-BV or mFOLFOX6-BV were comparable with those reported previously.
First-line FOLFIRI-BV and mFOLFOX6-BV had comparable PFS and OS, similar to results in patients with high baseline tumor ERCC1 levels. There were no new safety signals with these bevacizumab-containing regimens.
MAVERICC 比较了改良的亚叶酸/5-氟尿嘧啶/奥沙利铂联合贝伐珠单抗(mFOLFOX6-BV)与亚叶酸/5-氟尿嘧啶/伊立替康联合贝伐珠单抗(FOLFIRI-BV)在未经治疗的转移性结直肠癌(mCRC)患者中的疗效和安全性。MAVERICC 是一项全球性、随机、开放标签、二期研究。主要目的是评估(i)在接受 mFOLFOX6-BV 或 FOLFIRI-BV 治疗的未经治疗的 mCRC 患者中,切除修复交叉互补基因 1(ERCC1)表达与无进展生存期(PFS)之间的关系,以及(ii)患者血浆血管内皮生长因子 A(VEGF-A)与 PFS 之间的关系。在随机分组前,根据肿瘤 ERCC1/β-肌动蛋白 mRNA 表达水平和区域对患者进行分层。
在 376 名入组患者中,188 名患者分别接受了 mFOLFOX6-BV 和 FOLFIRI-BV 治疗。FOLFIRI-BV 和 mFOLFOX6-BV 的 PFS 和总生存期(OS)相当,FOLFIRI-BV 的 PFS 更高[风险比(HR)=0.79;95%置信区间(CI):0.61-1.01;P=0.06],OS 更高[HR=0.76;95%CI:0.56-1.04;P=0.09]。在高 ERCC1 亚组中,两组间 PFS 和 OS 相当(PFS,HR=0.84;95%CI:0.56-1.26;P=0.40;OS,HR=0.80;95%CI:0.51-1.26;P=0.33)。在各组治疗中,高血浆 VEGF-A 水平(>5.1pg/ml)与较短的 PFS(HR=1.19;95%CI:0.93-1.53;P=0.17)和显著较短的 OS(HR=1.64;95%CI:1.20-2.24;P<0.01)相关,而低水平(<=5.1pg/ml)则没有。FOLFIRI-BV 或 mFOLFOX6-BV 的安全性发现与以前报告的相似。
一线 FOLFIRI-BV 和 mFOLFOX6-BV 的 PFS 和 OS 相当,与基线肿瘤 ERCC1 水平较高的患者的结果相似。这些贝伐珠单抗联合方案没有新的安全性信号。