Anatomical benefit from ranibizumab treatment of predominantly classic neovascular age-related macular degeneration in the 2-year ANCHOR study

Srinivas R. Sadda, Glenn Stoller, David S. Boyer, Barbara A. Blodi, Howard Shapiro, Tsontcho Ianchulev

Research output: Contribution to journalArticlepeer-review

34 Scopus citations

Abstract

Purpose: To compare lesion anatomical responses to ranibizumab versus verteporfin photodynamic therapy (PDT) in the ANCHOR (Anti-VEGF Antibody for the Treatment of Predominantly Classic Choroidal Neovascularization [CNV] in Age-Related Macular Degeneration) study. Methods: In this 2-year, Phase III, randomized, multicenter, double-masked trial, 423 patients received ranibizumab (0.3 or 0.5 mg) monthly + sham PDT or PDT + monthly sham injection. Photodynamic therapy (or sham PDT) was administered at Day 0 and then quarterly as needed. A central reading center assessed fundus photography and fluorescein angiography images. A subset (n = 61) had optical coherence tomography assessments. Main outcome measures included mean change from baseline at Months 12 and 24 for area of classic CNV and total area of leakage from Cnv. Results: At Months 12 and 24, ranibizumab was superior to PDT (P < 0.0001) for mean changes from baseline in total area of lesion, CNV area, and total area CNV leakage. Month 12 optical coherence tomographies showed greater center point thickness decrease from baseline with ranibizumab than with PDT (P = 0.0003). Ranibizumab benefits over PDT were evident by 3 months (fluorescein angiography) and 7 days (optical coherence tomography). Conclusion: Differences between the PDT and the ranibizumab groups in lesion anatomical outcomes were early, sustained, and favored ranibizumab.

Original languageEnglish
Pages (from-to)1390-1399
Number of pages10
JournalRetina
Volume30
Issue number9
DOIs
StatePublished - Oct 2010
Externally publishedYes

Keywords

  • age-related macular degeneration, antiangiogenesis agents, choroidal neovascularization, ranibizumab, vascular endothelial growth factor, verteporfin photodynamic therapy

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