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复发性恶性脑胶质瘤中阿柏西普的 II 期研究:一项北美脑肿瘤联盟研究。

Phase II study of aflibercept in recurrent malignant glioma: a North American Brain Tumor Consortium study.

机构信息

The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

J Clin Oncol. 2011 Jul 1;29(19):2689-95. doi: 10.1200/JCO.2010.34.1636. Epub 2011 May 23.

Abstract

PURPOSE

Antivascular endothelial growth factor (anti-VEGF) therapy is a promising treatment approach for patients with recurrent glioblastoma. This single-arm phase II study evaluated the efficacy of aflibercept (VEGF Trap), a recombinantly produced fusion protein that scavenges both VEGF and placental growth factor in patients with recurrent malignant glioma.

PATIENTS AND METHODS

Forty-two patients with glioblastoma and 16 patients with anaplastic glioma who had received concurrent radiation and temozolomide and adjuvant temozolomide were enrolled at first relapse. Aflibercept 4 mg/kg was administered intravenously on day 1 of every 2-week cycle.

RESULTS

The 6-month progression-free survival rate was 7.7% for the glioblastoma cohort and 25% for patients with anaplastic glioma. Overall radiographic response rate was 24% (18% for glioblastoma and 44% for anaplastic glioma). The median progression-free survival was 24 weeks for patients with anaplastic glioma (95% CI, 5 to 31 weeks) and 12 weeks for patients with glioblastoma (95% CI, 8 to 16 weeks). A total of 14 patients (25%) were removed from the study for toxicity, on average less than 2 months from treatment initiation. The main treatment-related National Cancer Institute Common Terminology Criteria grades 3 and 4 adverse events (38 total) included fatigue, hypertension, and lymphopenia. Two grade 4 CNS ischemias and one grade 4 systemic hemorrhage were reported. Aflibercept rapidly decreases permeability on dynamic contrast enhanced magnetic resonance imaging, and molecular analysis of baseline tumor tissue identified tumor-associated markers of response and resistance.

CONCLUSION

Aflibercept monotherapy has moderate toxicity and minimal evidence of single-agent activity in unselected patients with recurrent malignant glioma.

摘要

目的

抗血管内皮生长因子(anti-VEGF)治疗是复发性胶质母细胞瘤患者有希望的治疗方法。这项单臂 II 期研究评估了 aflibercept(VEGF Trap)在复发性恶性神经胶质瘤患者中的疗效,aflibercept 是一种重组产生的融合蛋白,可清除 VEGF 和胎盘生长因子。

患者和方法

42 名胶质母细胞瘤患者和 16 名间变性神经胶质瘤患者在首次复发时接受了同步放疗和替莫唑胺及辅助替莫唑胺治疗。在每 2 周的周期的第 1 天,静脉内给予 aflibercept 4mg/kg。

结果

胶质母细胞瘤队列的 6 个月无进展生存率为 7.7%,间变性神经胶质瘤患者为 25%。总体放射学反应率为 24%(胶质母细胞瘤为 18%,间变性神经胶质瘤为 44%)。间变性神经胶质瘤患者的中位无进展生存期为 24 周(95%CI,5 至 31 周),胶质母细胞瘤患者为 12 周(95%CI,8 至 16 周)。共有 14 名患者(25%)因毒性而退出研究,平均在治疗开始后不到 2 个月。主要与治疗相关的美国国立癌症研究所常见不良事件术语标准 3 级和 4 级不良事件(共 38 项)包括疲劳、高血压和淋巴细胞减少症。报告了 2 例 4 级中枢神经系统缺血和 1 例 4 级全身性出血。aflibercept 可迅速降低动态对比增强磁共振成像的通透性,对基线肿瘤组织的分子分析确定了与反应和耐药相关的肿瘤相关标志物。

结论

在未经选择的复发性恶性神经胶质瘤患者中,aflibercept 单药治疗具有中度毒性和单一药物活性的最小证据。

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