Schauwvlieghe A M E, Dijkman G, Hooymans J M, Verbraak F D, Hoyng C B, Dijkgraaf M G W, Van Leeuwen R, Vingerling J R, Moll A C, Schlingemann Reinier O
Department of Ophthalmology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Department of Ophthalmology, Leiden University Medical Centre, Leiden, The Netherlands.
BMC Ophthalmol. 2015 Jul 7;15:71. doi: 10.1186/s12886-015-0043-x.
The effectiveness of ranibizumab in the treatment of diabetic macular edema has been proven with large clinical trials. For bevacizumab only two clinical trials have been published and a head-to-head comparison is lacking to date. However, if proved non-inferior to ranibizumab, use of the off-label bevacizumab could reduce costs enormously without a loss in visual acuity. A cost-effectiveness study has been designed to substantiate this hypothesis.
To compare the effectiveness and costs of 1.25 mg of bevacizumab to 0.5 mg ranibizumab given as monthly intravitreal injections during 6 months in patients with diabetic macular edema. It is hypothesized that bevacizumab is non-inferior to ranibizumab regarding its effectiveness.
This is a randomized, controlled, double masked, clinical trial in 246 patients in seven academic trial centres in The Netherlands.
The primary outcome measure is the change in best-corrected visual acuity (BCVA) in the study eye from baseline to month 6. Secondary outcomes are the proportions of patients with a gain or loss of 15 letters or more or a BCVA of 20/40 or more at 6 months, the change in leakage on fluorescein angiography and the change in foveal thickness by optical coherence tomography at 6 months, the number of adverse events in 6 months, and the costs per quality adjusted life-year of the two treatments.
雷珠单抗治疗糖尿病性黄斑水肿的有效性已在大型临床试验中得到证实。对于贝伐单抗,仅发表了两项临床试验,且迄今为止缺乏直接对比研究。然而,如果证明其不劣于雷珠单抗,使用未获批准的贝伐单抗可大幅降低成本且不影响视力。一项成本效益研究旨在证实这一假设。
比较糖尿病性黄斑水肿患者每月玻璃体内注射1.25 mg贝伐单抗与0.5 mg雷珠单抗,持续6个月的有效性和成本。假设贝伐单抗在有效性方面不劣于雷珠单抗。
这是一项在荷兰七个学术试验中心对246名患者进行的随机、对照、双盲临床试验。
主要结局指标是研究眼从基线到第6个月最佳矫正视力(BCVA)的变化。次要结局包括6个月时视力提高或降低15个字母及以上或BCVA达到20/40及以上的患者比例、荧光素血管造影渗漏情况的变化、6个月时光学相干断层扫描测量的黄斑中心凹厚度变化、6个月内不良事件的数量以及两种治疗方法每质量调整生命年的成本。