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Aflibercept 联合 FOLFOX 和氟嘧啶维持治疗转移性结直肠癌的一线疗效:GERCOR VELVET Ⅱ期研究。

Efficacy of aflibercept with FOLFOX and maintenance with fluoropyrimidine as first‑line therapy for metastatic colorectal cancer: GERCOR VELVET phase II study.

机构信息

Department of Medical Oncology, Franco‑British Institute, 92300 Levallois‑Perret, France.

Department of Gastroenterology, Sorbonne University, Pierre and Marie Curie University Paris 6, CH Universitaire Pitié‑Salpétrière, 75013 Paris, France.

出版信息

Int J Oncol. 2019 Apr;54(4):1433-1445. doi: 10.3892/ijo.2019.4709. Epub 2019 Feb 1.

DOI:10.3892/ijo.2019.4709
PMID:30720091
Abstract

Aflibercept in combination with 5‑fluorouracil (5‑FU)/irinotecan improves overall survival in the second‑line therapy of patients with metastatic colorectal cancer (mCRC). In this study, we evaluated the effects of aflibercept in first‑line therapy with FOLFOX followed by maintenance with fluoropyrimidine. VELVET was a prospective, single‑arm multicenter phase II study (completed). Patients with previously untreated, unresectable, evaluable or measurable mCRC, with an age ≥18 years, and an ECOG performance status of 0‑2 received 6 cycles of modified FOLFOX7 (5‑FU/folinic acid and oxaliplatin) with aflibercept at 4 mg/kg every 2 weeks followed by maintenance therapy with fluoropyrimidine with aflibercept until disease progression or limiting toxicity. The reintroduction of oxaliplatin was performed at first progression. The primary endpoint was progression‑free survival (PFS) at 6 months. From May, 2013 to May, 2014, 49 patients were included and 48 were evaluable for response. In total, 33 patients (67.4%) were alive without progression at 6 months. The Kaplan‑Meier survival 6‑month and 1‑year PFS rates were 79.1 and 36.1%, respectively, and the median PFS was 9.3 months (95% CI, 8.3‑12.5). The objective response rate was 59.2% (N=29/49). The most common (≥10%) grade 3‑4 adverse events were hypertension (23%), fatigue (15%), neutropenia (12%), neuropathy (12%) and stomatitis (10%). Three (6%) treatment‑related deaths occurred: One from stroke, one from pulmonary embolism and one from neutropenic sepsis. On the whole, this study demonstrates the efficacy of aflibercept in combination with an oxaliplatin‑based regimen in the first‑line therapy of patients with mCRC. A strict monitoring of blood pressure and immediate management of hypertension during therapy is mandatory.

摘要

阿柏西普联合氟尿嘧啶(5-FU)/伊立替康可改善转移性结直肠癌(mCRC)二线治疗患者的总生存期。本研究评估了阿柏西普在 FOLFOX 一线治疗后联合氟嘧啶维持治疗中的作用。VELVET 是一项前瞻性、单臂、多中心 II 期研究(已完成)。年龄≥18 岁、ECOG 体能状态 0-2 分、未经治疗、不可切除、可评估或可测量的 mCRC 患者,接受 6 个周期的改良 FOLFOX7(5-FU/亚叶酸钙和奥沙利铂)联合阿柏西普 4mg/kg,每 2 周 1 次,随后联合氟嘧啶维持治疗,直至疾病进展或出现不可耐受毒性。奥沙利铂在首次进展时重新使用。主要终点是 6 个月时的无进展生存期(PFS)。2013 年 5 月至 2014 年 5 月,共纳入 49 例患者,48 例可评估疗效。共有 33 例(67.4%)患者在 6 个月时无进展且存活。Kaplan-Meier 生存 6 个月和 1 年 PFS 率分别为 79.1%和 36.1%,中位 PFS 为 9.3 个月(95%CI,8.3-12.5)。客观缓解率为 59.2%(N=29/49)。最常见(≥10%)的 3-4 级不良事件包括高血压(23%)、乏力(15%)、中性粒细胞减少(12%)、周围神经病变(12%)和口腔炎(10%)。3 例(6%)治疗相关死亡:1 例死于中风,1 例死于肺栓塞,1 例死于中性粒细胞减少性败血症。总的来说,本研究表明阿柏西普联合奥沙利铂方案在 mCRC 患者的一线治疗中具有疗效。在治疗过程中必须严格监测血压并立即进行高血压管理。

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