Ranibizumab versus bevacizumab for ophthalmic diseases related to neovascularisation: a meta-analysis of randomised controlled trials.
Ranibizumab versus bevacizumab for ophthalmic diseases related to neovascularisation: a meta-analysis of randomised controlled trials.
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雷珠单抗与贝伐单抗治疗与新生血管相关的眼科疾病:随机对照试验的荟萃分析
DOI:
10.1371/journal.pone.0101253
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发表时间:
2014
期刊:
影响因子:
3.7
通讯作者:
Li J
中科院分区:
文献类型:
--
作者:
Wu B;Wu H;Liu X;Lin H;Li J
Bevacizumab is believed to be as effective and safe as ranibizumab for ophthalmic diseases; however, its magnitude of effectiveness and safety profile remain controversial. Thus, a meta-analysis and systematic review appears necessary. PubMed and EMBASE were systematically searched with no restrictions. All relevant citations comparing ranibizumab and bevacizumab were considered for inclusion. Pooled effect estimates were obtained using a fixed- and random-effects meta-analysis. Nine independent randomised-controlled clinical trials (RCTs) involving 2,289 participants were identified. Compared with bevacizumab, the overall combined weighted mean difference (WMD) of the mean change in visual acuity for ranibizumab was 0.52 letters (95% CI −0.11–1.14). The odds ratios (ORs) of gaining ≥15, gaining 5–14, losing 5–14 and losing ≤15 letters were 1.10 (95% CI 0.90–1.33), 0.93 (95% CI 0.77–1.11), 0.89 (95% CI 0.65–1.22) and 0.95 (95% CI 0.73–1.25), respectively. The risk of serious systemic events increased by 17% (95% CI 6%–27%, p = 0.0042) for bevacizumab treatment in comparison with ranibizumab. No statistically significant differences between the two treatments were found for the nonfatal arterial thrombotic events, ocular serious adverse, death from vascular and all causes events. Bevacizumab is not inferior to ranibizumab as a treatment for achieving visual acuity. The use of bevacizumab was associated with an increased risk of developing serious systemic events. Weighing the costs and health outcomes is necessary when selecting between bevacizumab and ranibizumab for ophthalmic diseases. Due to the limitations of the available data, further research is needed.
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DOI:
10.1136/bmj.e5182
发表时间:
2012-08-13
期刊:
BMJ (Clinical research ed.)
影响因子:
--
作者:
Ford JA;Elders A;Shyangdan D;Royle P;Waugh N
通讯作者:
Waugh N
影响因子:
--
作者:
Curtis, Lesley H.;Hammill, Bradley G.;Cousins, Scott W.
通讯作者:
Cousins, Scott W.
影响因子:
1.6
作者:
Hufendiek, Katerina;Hufendiek, Karsten;Gamulescu, Maria-Andreea
通讯作者:
Gamulescu, Maria-Andreea
影响因子:
--
作者:
Cho HJ;Baek JS;Lee DW;Kim CG;Kim JW
通讯作者:
Kim JW
影响因子:
4.2
作者:
Brechner, Ross J.;Rosenfeld, Philip J.;Caplan, Stuart
通讯作者:
Caplan, Stuart