Constable Ian J, Pierce Cora M, Lai Chooi-May, Magno Aaron L, Degli-Esposti Mariapia A, French Martyn A, McAllister Ian L, Butler Steve, Barone Samuel B, Schwartz Steven D, Blumenkranz Mark S, Rakoczy Elizabeth P
Lions Eye Institute, Nedlands, WA, Australia; Sir Charles Gairdner Hospital, Nedlands, WA, Australia; Centre for Ophthalmology and Visual Science, The University of Western Australia, Crawley, WA, Australia.
Lions Eye Institute, Nedlands, WA, Australia.
EBioMedicine. 2016 Dec;14:168-175. doi: 10.1016/j.ebiom.2016.11.016. Epub 2016 Nov 10.
We present the results of a Phase 2a randomized controlled trial investigating the safety, and secondary endpoints of subretinal rAAV.sFLT-1 gene therapy in patients with active wet age-related macular degeneration (wAMD).
All patients (n=32), (ClinicalTrials.gov; NCT01494805), received ranibizumab injections at baseline and week 4, and thereafter according to prespecified criteria. Patients in the gene therapy group (n=21) received rAAV.sFLT-1 (1×10vg). All patients were assessed every 4weeks to the week 52 primary endpoint.
Ocular adverse events (AEs) in the rAAV.sFLT-1 group were mainly procedure related and self-resolved. All 11 phakic patients in the rAAV.sFLT-1 group showed progression of cataract following vitrectomy. No systemic safety signals were observed and none of the serious AEs were associated with rAAV.sFLT-1. AAV2 capsid was not detected and rAAV.sFLT-1 DNA was detected transiently in the tears of 13 patients. ELISPOT analysis did not identify any notable changes in T-cell response. In the rAAV.sFLT-1 group 12 patients had neutralizing antibodies (nAb) to AAV2. There was no change in sFLT-1 levels in bodily fluids. In the rAAV.sFLT-1 group, Best Corrected Visual Acuity (BCVA) improved by a median of 1.0 (IQR: -3.0 to 9.0) Early Treatment Diabetic Retinopathy Study (ETDRS) letters from baseline compared to a median of -5.0 (IQR: -17.5 to 1.0) ETDRS letters change in the control group. Twelve (57%) patients in the rAAV.sFLT-1 group maintained or improved vision compared to 4 (36%) in the control group. The median number of ranibizumab retreatments was 2.0 (IQR: 1.0 to 6.0) for the gene therapy group compared to 4.0 (IQR: 3.5 to 4.0) for the control group. Interpretation rAAV.sFLT-1 combined with the option for co-treatment appears to be a safe and promising approach to the treatment of wAMD.
National Health and Medical Research Council of Australia (AP1010405), Lions Eye Institute, Perth Australia, Avalanche Biotechnologies, Menlo Pk, CA, USA.
我们展示了一项2a期随机对照试验的结果,该试验旨在研究视网膜下注射重组腺相关病毒载体sFLT-1基因疗法在活动性湿性年龄相关性黄斑变性(wAMD)患者中的安全性及次要终点。
所有患者(n = 32;ClinicalTrials.gov;NCT01494805)在基线和第4周接受雷珠单抗注射,此后根据预先设定的标准进行注射。基因治疗组(n = 21)的患者接受rAAV.sFLT-1(1×10vg)治疗。所有患者每4周评估一次,直至第52周的主要终点。
rAAV.sFLT-1组的眼部不良事件(AE)主要与手术相关且可自行缓解。rAAV.sFLT-1组的所有11例有晶状体患者在玻璃体切除术后均出现白内障进展。未观察到全身安全信号,且没有严重不良事件与rAAV.sFLT-1相关。未检测到AAV2衣壳,13例患者的泪液中短暂检测到rAAV.sFLT-1 DNA。ELISPOT分析未发现T细胞反应有任何显著变化。rAAV.sFLT-1组中有12例患者对AAV2有中和抗体(nAb)。体液中sFLT-1水平无变化。在rAAV.sFLT-1组中,最佳矫正视力(BCVA)较基线时平均提高了1.0(四分位间距:-3.0至9.0)个早期糖尿病性视网膜病变研究(ETDRS)字母,而对照组的平均变化为-5.0(四分位间距:-17.5至1.0)个ETDRS字母。rAAV.sFLT-1组中有12例(57%)患者视力维持或改善,而对照组为4例(36%)。基因治疗组雷珠单抗再次治疗的中位数为2.0(四分位间距:1.0至6.0),而对照组为4.0(四分位间距:3.5至4.0)。解读:rAAV.sFLT-1联合联合治疗方案似乎是一种安全且有前景的wAMD治疗方法。
澳大利亚国家卫生与医学研究委员会(AP1010405)、澳大利亚珀斯狮子眼研究所、美国加利福尼亚州门洛帕克市雪崩生物技术公司。