Department of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Clin Neurol Neurosurg. 2020 Nov;198:106239. doi: 10.1016/j.clineuro.2020.106239. Epub 2020 Sep 20.
Based on the effective radiological responses, bevacizumab (BEV) has been widely used in the treatment of recurrent high-grade glioma. Although the current standard dose is 5 mg/kg/week, the optimal dosage of BEV is controversial, as few dose-response studies have been performed in recent years. Therefore, we conducted a meta-analysis to explore the value of reduced-dose bevacizumab versus standard-dose bevacizumab in recurrent high-grade glioma treatment.
Three major electronic databases (PubMed, EMBASE and the Cochrane Library) were searched for eligible documents published before February 2020. Literature on low-dose bevacizumab versus conventional dose in progressive high-grade glioma was included, and the endpoints of eligible researches should be progression-free survival (PFS) and overall survival (OS). All available data were collected and then analyzed with Stata software.
Four cohort studies were evaluated, including 552 patients (reduced-dose BEV group: 257, standard-dose BEV group: 295). Low dose BEV seems to slightly improve survival compared to conventional dose as HR < 1 indicates a protective effect, but no significant differences in OS (HR 0.77; 95 % CI 0.53-1.10; P = 0.151) and PFS (HR 0.66; 95 % CI 0.37-1.20; P = 0.175) were found between the two groups in this study.
Reduced-dose bevacizumab schedule resulted in similar OS and PFS to standard-dose bevacizumab in recurrent high-grade glioma, with less side effects and less cost of treatment. Therefore, low-dose bevacizumab represents a promising therapeutic option for recurrent high-grade glioma patients. Further prospective randomized trials are needed to confirm our results.
基于有效的放射学反应,贝伐单抗(bevacizumab,BEV)已广泛用于复发性高级别胶质瘤的治疗。尽管目前的标准剂量为 5mg/kg/周,但 BEV 的最佳剂量仍存在争议,因为近年来很少有剂量反应研究。因此,我们进行了一项荟萃分析,以探讨降低剂量贝伐单抗与标准剂量贝伐单抗在复发性高级别胶质瘤治疗中的价值。
检索了三个主要的电子数据库(PubMed、EMBASE 和 Cochrane Library),检索时间截至 2020 年 2 月之前发表的符合条件的文献。纳入了低剂量贝伐单抗与常规剂量贝伐单抗治疗进展性高级别胶质瘤的文献,符合条件的研究终点应为无进展生存期(progression-free survival,PFS)和总生存期(overall survival,OS)。收集所有可用数据,并使用 Stata 软件进行分析。
评估了 4 项队列研究,共纳入 552 例患者(低剂量 BEV 组:257 例,标准剂量 BEV 组:295 例)。低剂量 BEV 似乎比常规剂量略微改善了生存,因为 HR<1 表明具有保护作用,但两组之间 OS(HR 0.77;95%CI 0.53-1.10;P=0.151)和 PFS(HR 0.66;95%CI 0.37-1.20;P=0.175)无显著差异。
在复发性高级别胶质瘤中,降低剂量贝伐单抗方案与标准剂量贝伐单抗方案的 OS 和 PFS 相似,且副作用更少,治疗费用更低。因此,低剂量贝伐单抗代表了复发性高级别胶质瘤患者的一种有前途的治疗选择。需要进一步的前瞻性随机试验来证实我们的结果。