University of Witwatersrand Faculty of Health Sciences, Johannesburg, South Africa.
University Hospitals Leuven and KU Leuven, Belgium.
J Geriatr Oncol. 2018 Jan;9(1):32-39. doi: 10.1016/j.jgo.2017.07.010. Epub 2017 Aug 12.
Aflibercept (ziv-aflibercept) significantly improves progression-free (PFS) and overall survival (OS) when added to 5-fluorouracil, leucovorin and irinotecan (FOLFIRI), compared with FOLFIRI alone, in patients with metastatic colorectal cancer previously treated with oxaliplatin-based therapy. This subset analysis of the VELOUR study investigates aflibercept plus FOLFIRI versus placebo plus FOLFIRI according to age.
Efficacy and safety were analyzed by treatment arm and age (≥ or <65years).
Overall, 443 patients were ≥65years old (205 in aflibercept arm; 238 in placebo arm) and 783 were <65years old (407 in aflibercept arm; 376 in placebo arm). Median OS was 12.6 versus 11.3months (hazard ratio [HR]: 0.85; 95.34% CI 0.68-1.07) in patients ≥65years old and 14.5 versus 12.5months (HR: 0.80; 95.34% CI 0.67-0.95) in those patients <65years old, for patients receiving FOLFIRI plus aflibercept or placebo, respectively. There was no interaction between treatment and age. Treatment-emergent adverse events (AEs) were comparable for patients <65years and ≥65years old. The incidence of grade 3/4 AEs was higher for patients ≥65years old than for those <65years old in both the aflibercept (89.3% versus 80.5%) and placebo (67.4% versus 59.4%) arms. Interaction tests for grade 3/4 antiangiogenic agent-related AEs suggested no heterogeneity between the older and younger patient populations (p>0.1).
A limited but consistent benefit on both OS and PFS was associated with the addition of aflibercept to FOLFIRI compared with placebo in patients <65 and ≥65years old, with a marked but manageable increase in the toxicity profile in older patients.
clinicaltrials.govNCT00561470.
与单独使用 FOLFIRI 相比,在先前接受奥沙利铂为基础的治疗的转移性结直肠癌患者中,阿柏西普(ziv-aflibercept)与 5-氟尿嘧啶、亚叶酸钙和伊立替康(FOLFIRI)联合使用可显著改善无进展生存期(PFS)和总生存期(OS)。这项 VELOUR 研究的亚组分析根据年龄调查了阿柏西普联合 FOLFIRI 与安慰剂联合 FOLFIRI 的疗效。
根据治疗组和年龄(≥65 岁或<65 岁)分析疗效和安全性。
共有 443 名患者年龄≥65 岁(阿柏西普组 205 名;安慰剂组 238 名),783 名患者年龄<65 岁(阿柏西普组 407 名;安慰剂组 376 名)。中位 OS 分别为 12.6 个月和 11.3 个月(危险比[HR]:0.85;95.34%CI 0.68-1.07),在≥65 岁的患者中接受 FOLFIRI 联合阿柏西普或安慰剂治疗的患者中;14.5 个月和 12.5 个月(HR:0.80;95.34%CI 0.67-0.95),在年龄<65 岁的患者中。治疗与年龄之间无交互作用。在年龄<65 岁和≥65 岁的患者中,治疗相关不良事件(AE)发生率相当。在阿柏西普(89.3%比 80.5%)和安慰剂(67.4%比 59.4%)组中,年龄≥65 岁的患者出现 3/4 级 AE 的发生率高于年龄<65 岁的患者。对 3/4 级抗血管生成药物相关 AE 的交互检验表明,老年和年轻患者人群之间没有异质性(p>0.1)。
与安慰剂相比,在年龄<65 岁和≥65 岁的患者中,阿柏西普联合 FOLFIRI 治疗可显著改善 OS 和 PFS,在老年患者中,毒性谱显著但可管理。
clinicaltrials.govNCT00561470。