Systematic review and network meta-analysis of the efficacy of existing treatments for patients with recurrent glioblastoma

被引:18
作者
Schritz, Anna [1 ]
Aouali, Nassera [2 ]
Fischer, Aurelie [2 ]
Dessenne, Coralie [5 ]
Adams, Roisin [6 ]
Berchem, Guy [3 ,4 ]
Huiart, Laetitia [5 ]
Schmitz, Susanne [1 ]
机构
[1] Luxembourg Inst Hlth, Dept Populat Hlth, Competence Ctr Methodol & Stat, Strassen, Luxembourg
[2] Luxembourg Inst Hlth, Clin & Epidemiol Invest Ctr, Dept Populat Hlth, Strassen, Luxembourg
[3] Ctr Hosp Luxembourg, Dept Hematooncol, Luxembourg, Luxembourg
[4] Luxembourg Inst Hlth, Strassen, Luxembourg
[5] Luxembourg Inst Hlth, Dept Populat Hlth, Strassen, Luxembourg
[6] Natl Ctr Pharmacoecon, Dublin, Ireland
关键词
network meta-analysis; overall survival; progression-free survival; recurrent glioblastoma; systematic review; BEVACIZUMAB PLUS LOMUSTINE; PHASE-II; RESPONSE ASSESSMENT; COMBINATION; SURVIVAL; CHEMOTHERAPY; PROGRESSION; MULTIFORME; CRITERIA; THERAPY;
D O I
10.1093/noajnl/vdab052
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Despite advances in the treatment of cancers over the last years, treatment options for patients with recurrent glioblastoma (rGBM) remain limited with poor outcomes. Many regimens have been investigated in clinical trials; however, there is a lack of knowledge on comparative effectiveness. The aim of this systematic review is to provide an overview of existing treatment strategies and to estimate the relative efficacy of these regimens in terms of progression-free survival (PFS) and overall survival (OS). Methods. We conducted a systematic review to identify randomized controlled trials (RCTs) investigating any treatment regimen in adult patients suffering from rGBM. Connected studies reporting at least one of our primary outcomes were included in a Bayesian network meta-analysis (NMA) estimating relative treatment effects. Results. Forty RCTs fulfilled our inclusion criteria evaluating the efficacy of 38 drugs as mono- or combination therapy. Median OS ranged from 2.9 to 18.3 months; median PFS ranged from 0.7 to 6 months. We performed an NMA including 24 treatments that were connected within a large evidence network. Our NMA indicated improvement in PFS with most bevacizumab (BV)-based regimens compared to other regimens. We did not find any differences in OS between treatments. Conclusion. This systematic review provides a comprehensive overview of existing treatment options for rGBM. The NMA provides relative effects for many of these treatment regimens, which have not been directly compared in RCTs. Overall, outcomes for patients with rGBM remain poor across all treatment options, highlighting the need for innovative treatment options.
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页数:12
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