Kokame Gregg T, Lai James C, Wee Raymond, Yanagihara Ryan, Shantha Jessica G, Ayabe Julia, Hirai Kelsi
Division of Ophthalmology, Department of Surgery, University of Hawaii School of Medicine, 651 IIalo St, Honolulu, HI, 96813, USA.
The Retina Center at Pali Momi, 98-1079 Moanalua Road, Suite 470, Aiea, Hawaii, 96701, USA.
BMC Ophthalmol. 2016 Jul 27;16:127. doi: 10.1186/s12886-016-0305-2.
Polypoidal choroidal vasculopathy is a variant of choroidal neovascularization and neovascular age related macular degeneration presenting with hemorrhagic and exudative changes within the macula and/or peripapillary region leading to vision loss. In contrast to neovascular age related macular degeneration, polypoidal choroidal vasculopathy has differing clinical manifestations and treatment strategies. Historically, polypoidal choroidal vasculopathy complexes are less responsive to anti-vascular endothelial growth factor therapy with no prospective clinical trials evaluating aflibercept in management of polypoidal choroidal vasculopathy. Herein we prospectively evaluate the efficacy and safety of intravitreal aflibercept in polypoidal choroidal vasculopathy.
A prospective, open-label, investigator-sponsored trial of intravitreal aflibercept for polypoidal choroidal vasculopathy in 21 eyes was conducted. Injections were administered monthly for 3 initial treatments, then every other month with monthly evaluations. The primary outcome measures were the mean change in best corrected visual acuity and adverse events. Secondary outcome measures included stabilization of vision, presence of subretinal hemorrhage, serous detachment, retinal pigment epithelial detachment, and regression of polypoidal complexes on indocyanine green angiography.
At 6 months, the median visual acuity was 20/40 (range 20/25-20/200) with a mean Early Treatment Diabetic Retinopathy Study vision of 68.4 letters. There was a gain of 2.76 Early Treatment Diabetic Retinopathy Study letters at 6 months (p = 0.15). No patient developed severe vision loss (≤15 letters) and vision was stable or improved in 19/21 eyes (91 %). Subretinal fluid resolved in 13/18 eyes (72 %), and subretinal hemorrhage resolved in 6/8 eyes (75 %) respectively. The polyps regressed in 14/21 eyes (67 %) and the branching vascular network decreased in 1 eye and was stable in all other eyes. The retinal pigment epithelial detachment improved in 13/15 eyes (87 %). Bimonthly treatment occurred in 15/21 patients (71 %). There were no adverse events.
Intravitreal aflibercept results in stabilization of vision, resolution of exudative and hemorrhagic complications with regression of polyps in polypoidal choroidal vasculopathy. Eyes with polypoidal choroidal vasculopathy previously treated with ranibizumab and bevacizumab can show marked improvement in the retinal pigment epithelial detachments and persistent polyps with aflibercept therapy.
Clinical trials.gov NCT01871376 , June 4(th) 2013.
息肉样脉络膜血管病变是脉络膜新生血管和新生血管性年龄相关性黄斑变性的一种变体,表现为黄斑和/或视乳头周围区域出现出血和渗出性改变,导致视力丧失。与新生血管性年龄相关性黄斑变性不同,息肉样脉络膜血管病变有不同的临床表现和治疗策略。从历史上看,息肉样脉络膜血管病变复合体对抗血管内皮生长因子治疗反应较差,尚无前瞻性临床试验评估阿柏西普治疗息肉样脉络膜血管病变的效果。在此,我们前瞻性评估玻璃体内注射阿柏西普治疗息肉样脉络膜血管病变的疗效和安全性。
进行了一项前瞻性、开放标签、研究者发起的试验,对21只眼睛的息肉样脉络膜血管病变采用玻璃体内注射阿柏西普治疗。最初3次治疗每月注射一次,之后每两个月注射一次,并每月进行评估。主要观察指标为最佳矫正视力的平均变化和不良事件。次要观察指标包括视力稳定情况、视网膜下出血情况、浆液性脱离、视网膜色素上皮脱离以及吲哚菁绿血管造影显示的息肉样复合体消退情况。
6个月时,中位视力为20/40(范围20/25 - 20/200),平均早期糖尿病性视网膜病变研究视力为68.4个字母。6个月时早期糖尿病性视网膜病变研究字母数增加了2.76个(p = 0.15)。没有患者出现严重视力丧失(≤15个字母),21只眼中19只(91%)视力稳定或改善。视网膜下液在18只眼中的13只(72%)消退,视网膜下出血在8只眼中的6只(75%)消退。息肉在21只眼中的14只(67%)消退,分支血管网在1只眼中减少,在其他所有眼中保持稳定。视网膜色素上皮脱离在15只眼中的13只(87%)得到改善。21例患者中有15例(71%)接受了每两个月一次的治疗。未出现不良事件。
玻璃体内注射阿柏西普可使息肉样脉络膜血管病变的视力稳定,渗出性和出血性并发症消退,息肉消退。先前接受雷珠单抗和贝伐单抗治疗的息肉样脉络膜血管病变的眼睛,采用阿柏西普治疗后,视网膜色素上皮脱离和持续性息肉可显著改善。
ClinicalTrials.gov NCT01871376,2013年6月4日。