Twenty‐four‐month real‐life treatment outcomes of polypoidal choroidal vasculopathy versus type 1 macular neovascularization in Caucasians

Author:

Airaldi Matteo1ORCID,Invernizzi Alessandro12ORCID,Nguyen Vuong2ORCID,Vujosevic Stela34ORCID,Ricci Federico5ORCID,Monaco Pietro6,Nassisi Marco7ORCID,Barthelmes Daniel28ORCID,Gillies Mark2ORCID,Viola Francesco79ORCID

Affiliation:

1. Eye Clinic, Department of Biomedical and Clinical Science Luigi Sacco, Luigi Sacco Hospital University of Milan Milan Italy

2. Save Sight Institute, Discipline of Ophthalmology The University of Sydney, Sydney Medical School Sydney New South Wales Australia

3. Department of Biomedical, Surgical and Dental Sciences University of Milan Milan Italy

4. Eye Clinic IRCCS MultiMedica Milan Italy

5. Department of Experimental Medicine Tor Vergata University Roma Italy

6. Ophthalmology Department San Martino Hospital Belluno Italy

7. Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milan Italy

8. University Hospital Zurich and University of Zurich Zurich Switzerland

9. Department of Clinical Sciences and Community Health University of Milan Milan Italy

Abstract

AbstractBackgroundTo compare 24‐month real‐world outcomes of Vascular Endothelial Growth Factor (VEGF) inhibitors for Polypoidal Choroidal Vasculopathy (PCV) and type 1 Macular Neovascularization (MNV) in a Caucasian population.MethodsRetrospective analysis from a prospectively designed observational database. Data from Italian centres participating in the Fight Retinal Blindness! (FRB!) project were collected. Treatment‐naïve PCV or type 1 MNV commencing treatment after January 2009 were included. The primary outcome was 24‐month visual acuity (VA) change; other outcomes included baseline characteristics, number of anti‐VEGF injections, time to lesion inactivation and proportion of active visits.ResultsA total of 322 eyes (114 PCVs) from 291 patients were included. Median [Q1, Q3] VA at baseline was comparable (70 [55, 75.8] vs. 70 [58.8, 75] letters, p = 0.95). Adjusted VA change at 2 years was higher in PCV (mean [95% CI], +1.2 [−1.6, 4.1] vs. −3.6 [−6, −1.2] letters, p = 0.005). PCV received fewer anti‐VEGF injections over the first 24 months of treatment than type 1 MNV (median [Q1, Q3], 8 [5, 10] vs. 9 [7, 12.2] injections, p = 0.001), inactivated earlier (median [Q1, Q3], 235 [184, 308] vs. 252 [169, 343] days, p = 0.04) and was less frequently graded ‘active’ (62% vs. 68% of visits, p = 0.001).ConclusionsPCV had slightly better VA outcomes over 24 months of treatment than type 1 MNV after receiving less anti‐VEGF injections. These results suggest a possible overlap of the two clinical entities with similar visual prognosis in Caucasians.

Funder

Novartis

Publisher

Wiley

Subject

Ophthalmology

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