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首页> 外文期刊>Journal of Clinical Oncology >Phase II study of aflibercept in recurrent malignant glioma: a north american brain tumor consortium study.
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Phase II study of aflibercept in recurrent malignant glioma: a north american brain tumor consortium study.

机译:阿柏西普在复发性恶性神经胶质瘤中的II期研究:一项北美脑肿瘤联合研究。

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摘要

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.
机译: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的一种有前途的治疗方法。这项单臂II期研究评估了aflibercept(VEGF Trap)(一种重组产生的融合蛋白,可清除VEGF和胎盘生长因子)在复发性恶性神经胶质瘤患者中的疗效。患者与方法:首次复发时同时接受放疗,替莫唑胺和替莫唑胺辅助治疗的42例胶质母细胞瘤患者和16例间变性胶质瘤患者。在每2周周期的第1天静脉注射Aflibercept 4 mg / 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%,间变性胶质瘤为44%)。间变性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(125%CI,8至16周)。总共有14名患者(25%)因毒性反应而从研究中移除,平均从治疗开始不到2个月。与治疗有关的主要国家癌症研究所通用术语标准3级和4级不良事件(共38个)包括疲劳,高血压和淋巴细胞减少。据报道有2例4级中枢神经系统缺血和1例4级全身性出血。 Aflibercept在动态对比增强的磁共振成像上迅速降低了通透性,并且基线肿瘤组织的分子分析确定了与肿瘤相关的反应和抵抗力标记。结论:Ablibercept单一疗法对未选出的复发性恶性神经胶质瘤患者具有中等毒性,单药活性的证据极少。

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