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2a期随机临床试验:视网膜下注射重组腺相关病毒.sFLT-1治疗湿性年龄相关性黄斑变性的安全性及事后分析

Phase 2a Randomized Clinical Trial: Safety and Post Hoc Analysis of Subretinal rAAV.sFLT-1 for Wet Age-related Macular Degeneration.

作者信息

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

机构信息

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.

出版信息

EBioMedicine. 2016 Dec;14:168-175. doi: 10.1016/j.ebiom.2016.11.016. Epub 2016 Nov 10.

Abstract

BACKGROUND

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).

METHODS

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.

FINDINGS

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.

FUNDING

National Health and Medical Research Council of Australia (AP1010405), Lions Eye Institute, Perth Australia, Avalanche Biotechnologies, Menlo Pk, CA, USA.

摘要

背景

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。

方法

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。

研究结果

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。

资助

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a66/5161436/53c4025eb0ee/gr1.jpg

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