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首页> 外文期刊>Journal of neuro-oncology. >Phase II study of metronomic chemotherapy with bevacizumab for recurrent glioblastoma after progression on bevacizumab therapy.
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Phase II study of metronomic chemotherapy with bevacizumab for recurrent glioblastoma after progression on bevacizumab therapy.

机译:贝伐珠单抗治疗进展后复发性胶质母细胞瘤的化疗方案的II期临床研究。

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摘要

We evaluated the efficacy of metronomic etoposide or temozolomide administered with bevacizumab among recurrent glioblastoma (GBM) patients who progressed on prior bevacizumab therapy in a phase 2, open-label, two-arm trial. Twenty-three patients received bevacizumab (10 mg/kg) every 2 weeks with either oral etoposide (50 mg/m2) daily for 21 consecutive days each month or daily temozolomide (50 mg/m2). The primary endpoint was 6-month progression-free survival (PFS-6) and secondary endpoints included safety and overall survival. Both the etoposide and temozolomide arms of the study closed at the interim analysis due to lack of adequate anti-tumor activity. No radiographic responses were observed. Although 12 patients (52%) achieved stable disease, PFS-6 was 4.4% and the median PFS was 7.3 weeks. The only grade 4 adverse event was reversible neutropenia. Grade 3 toxicities included fatigue (n = 2) and infection (n = 1). Metronomic etoposide or temozolomide is ineffective when administered with bevacizumab among recurrent GBM patients who have progressed on prior bevacizumab therapy. Alternative treatment strategies remain critically needed for this indication.
机译:我们在2期,开放标签,两臂试验的复发性胶质母细胞瘤(GBM)患者中,对先前使用贝伐单抗治疗进展的复发性胶质母细胞瘤(GBM)患者,评估了与贝伐单抗一起施用的节律性依托泊苷或替莫唑胺的疗效。 23例患者每2周接受贝伐单抗(10 mg / kg),每月连续21天每天口服依托泊苷(50 mg / m2)或每日替莫唑胺(50 mg / m2)。主要终点为6个月无进展生存期(PFS-6),次要终点为安全性和总体生存期。由于缺乏足够的抗肿瘤活性,该研究的依托泊苷和替莫唑胺均在中期分析中关闭。没有观察到射线照相反应。尽管12例患者(52%)病情稳定,但PFS-6为4.4%,中位PFS为7.3周。唯一的4级不良事件是可逆性中性粒细胞减少。 3级毒性包括疲劳(n = 2)和感染(n = 1)。在先前接受贝伐单抗治疗的GBM复发患者中,与贝伐单抗一起给药时,节律性依托泊苷或替莫唑胺无效。对于这种适应症,仍然迫切需要替代治疗策略。

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