Abstract

BackgroundPolypoidal 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.MethodsA 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.ResultsAt 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.ConclusionsIntravitreal 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.Trial registrationClinical trials.gov NCT01871376, June 4th 2013Electronic supplementary materialThe online version of this article (doi:10.1186/s12886-016-0305-2) contains supplementary material, which is available to authorized users.

Highlights

  • 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

  • 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

  • Since many of the fundus and optical coherence tomography (OCT) findings are similar to typical exudative age related macular degeneration (AMD), indocyanine green (ICG) angiography is essential to diagnosing Polypoidal choroidal vasculopathy (PCV) [1, 5]

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Summary

Introduction

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. Patients with PCV present with subretinal hemorrhage, subretinal fluid, and retinal pigment epithelial detachment (RPED) These findings are associated with a subretinal branching vascular network (BVN) with characteristic “polyplike” structures at the terminal ends of the vessels [1,2,3,4,5]. The treatment of the hemorrhagic and exudative complications of PCV is not well defined, but therapeutic approaches include photodynamic therapy (PDT), anti-vascular endothelial growth factor (VEGF) therapy, combined PDT and anti-VEGF therapy, direct thermal laser to polyps, and surgical management of significant subretinal hemorrhage or hemorrhagic retinal detachment [10]. Photodynamic therapy has been the mainstay of treatment in Asia for years [11,12,13,14], and was supported by an expert panel on PDT management in Asia This treatment is usually guided by the size of the complex on ICG angiography. Polypoidal choroidal vasculopathy is much more common in Asian populations and is being increasingly recognized in White populations with more frequent use of ICG angiography [3, 15,16,17,18,19,20]

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