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ESMO consensus guidelines for the management of patients with metastatic colorectal cancer.ESMO 共识指南:转移性结直肠癌患者的管理。
Ann Oncol. 2016 Aug;27(8):1386-422. doi: 10.1093/annonc/mdw235. Epub 2016 Jul 5.
2
Randomized phase III study of bevacizumab plus FOLFIRI and bevacizumab plus mFOLFOX6 as first-line treatment for patients with metastatic colorectal cancer (WJOG4407G).贝伐珠单抗联合 FOLFIRI 和贝伐珠单抗联合 mFOLFOX6 作为转移性结直肠癌一线治疗的随机 III 期研究(WJOG4407G)。
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Changes in expression levels of ERCC1, DPYD, and VEGFA mRNA after first-line chemotherapy of metastatic colorectal cancer: results of a multicenter study.转移性结直肠癌一线化疗后ERCC1、DPYD和VEGFA mRNA表达水平的变化:一项多中心研究的结果
Oncotarget. 2015 Oct 20;6(32):34004-13. doi: 10.18632/oncotarget.5227.
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ERCC1 Induction after Oxaliplatin Exposure May Depend on KRAS Mutational Status in Colorectal Cancer Cell Line: In Vitro Veritas.奥沙利铂暴露后 ERCC1 的诱导可能依赖于结直肠癌细胞系中的 KRAS 突变状态:体外真相。
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Prognostic value of KRAS mutations in stage III colon cancer: post hoc analysis of the PETACC8 phase III trial dataset.KRAS 突变在 III 期结肠癌中的预后价值:PETACC8 三期临床试验数据集的事后分析。
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A three-gene signature as potential predictive biomarker for irinotecan sensitivity in gastric cancer.一种三基因特征作为胃癌中伊立替康敏感性的潜在预测生物标志物。
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KRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markers.KRAS 基因突变状态与结直肠癌生存的关系:相关肿瘤标志物的联合影响。
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Markers of response for the antiangiogenic agent bevacizumab.抗血管生成药物贝伐珠单抗的反应标志物。
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Predictive impact of circulating vascular endothelial growth factor in four phase III trials evaluating bevacizumab.在四项评估贝伐珠单抗的 III 期临床试验中循环血管内皮生长因子的预测影响。
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MAVERICC:贝伐珠单抗联合 mFOLFOX6 与贝伐珠单抗联合 FOLFIRI 一线治疗转移性结直肠癌的随机、生物标志物分层、Ⅱ期研究

MAVERICC, a Randomized, Biomarker-stratified, Phase II Study of mFOLFOX6-Bevacizumab versus FOLFIRI-Bevacizumab as First-line Chemotherapy in Metastatic Colorectal Cancer.

机构信息

Division of Hematology and Oncology, Massachusetts General Hospital, Boston, Massachusetts.

Division of Hematology/Oncology, University of California Irvine, Irvine, California.

出版信息

Clin Cancer Res. 2019 May 15;25(10):2988-2995. doi: 10.1158/1078-0432.CCR-18-1221. Epub 2018 Sep 17.

DOI:10.1158/1078-0432.CCR-18-1221
PMID:30224341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9022943/
Abstract

PURPOSE

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

结果

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。

结论

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。