Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
IRIS® Registry analysis of anti-VEGF treatment in patients with coexisting neovascular age-related macular degeneration and geographic atrophy
Author Affiliations & Notes
  • Theodore Leng
    Byers Eye Institute at Stanford, Stanford University School of Medicine, Stanford, California, United States
  • Eric Schneider
    Tennessee Retina, Nashville, Tennessee, United States
  • Ehsan Rahimy
    Byers Eye Institute at Stanford, Stanford University School of Medicine, Stanford, California, United States
    Palo Alto Medical Foundation, Palo Alto, California, United States
  • Durga Borkar
    Duke University Department of Ophthalmology, Durham, North Carolina, United States
  • Jennifer Harris
    Verana Health, San Francisco, California, United States
  • Kristin Arkin-Leydig
    Verana Health, San Francisco, California, United States
  • Roy Schwartz
    Apellis Pharmaceuticals Inc, Zug, Switzerland
  • Daniel Jones
    Apellis Pharmaceuticals Inc, Waltham, Massachusetts, United States
  • Rushi Shah
    Apellis Pharmaceuticals Inc, Waltham, Massachusetts, United States
  • Brandon Coughlin
    Apellis Pharmaceuticals Inc, Waltham, Massachusetts, United States
  • Caroline Baumal
    Apellis Pharmaceuticals Inc, Waltham, Massachusetts, United States
  • Footnotes
    Commercial Relationships   Theodore Leng Alcon, Apellis Pharmaceuticals, Astellas, Boehringer Ingelheim, Graybug, Nanoscope Therapeutics, Protagonist Therapeutics, Regeneron, Roche/Genentech, Verana Health, Code C (Consultant/Contractor), Astellas, Code F (Financial Support); Eric Schneider Apellis Pharmaceuticals, Code C (Consultant/Contractor); Ehsan Rahimy Apellis Pharmaceuticals, Code C (Consultant/Contractor), Apellis Pharmaceuticals, Code F (Financial Support); Durga Borkar Apellis Pharmaceuticals, Code C (Consultant/Contractor); Jennifer Harris Apellis Pharmaceuticals, Code C (Consultant/Contractor); Kristin Arkin-Leydig Apellis Pharmaceuticals, Code C (Consultant/Contractor); Roy Schwartz Apellis Pharmaceuticals, Code E (Employment), Apellis Pharmaceuticals, Code O (Owner); Daniel Jones Apellis Pharmaceuticals, Code E (Employment), Apellis Pharmaceuticals, Code O (Owner); Rushi Shah Apellis Pharmaceuticals, Code E (Employment), Apellis Pharmaceuticals, Code O (Owner); Brandon Coughlin Apellis Pharmaceuticals, Code E (Employment), Apellis Pharmaceuticals, Code O (Owner); Caroline Baumal Apellis Pharmaceuticals, Code E (Employment), Apellis Pharmaceuticals, Code O (Owner)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 6491. doi:
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      Theodore Leng, Eric Schneider, Ehsan Rahimy, Durga Borkar, Jennifer Harris, Kristin Arkin-Leydig, Roy Schwartz, Daniel Jones, Rushi Shah, Brandon Coughlin, Caroline Baumal; IRIS® Registry analysis of anti-VEGF treatment in patients with coexisting neovascular age-related macular degeneration and geographic atrophy. Invest. Ophthalmol. Vis. Sci. 2024;65(7):6491.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Geographic atrophy (GA) and neovascular age-related macular degeneration (nAMD) are features of advanced AMD and may manifest simultaneously. There is limited data on outcomes in eyes with combined GA and nAMD. This retrospective cohort study analyzed American Academy of Ophthalmology IRIS Registry (Intelligent Research in Sight) data to characterize clinical features and anti-VEGF treatment outcomes in patients diagnosed with coexisting GA and nAMD.

Methods : Patients with ICD-10 codes for nAMD and GA in the same eye were identified in the IRIS registry between 7/1/2016 and 12/31/2021. Index date was defined as the first observed anti-VEGF injection. Anti-VEGF injection in the same eye within 36 months following GA diagnosis and at least one visual acuity (VA) measurement within 6 months prior to first injection were required. Eyes were divided into: Cohort 1; GA diagnosis following nAMD diagnosis, Cohort 2; GA diagnosis prior to nAMD diagnosis, and Cohort 3; coincident GA and nAMD diagnosis. GA treatment was not given in any eye. Demographics, clinical characteristics, anti-VEGF treatment patterns, VA and adverse events were assessed.

Results : Overall, 93,786 eyes with an ICD-10 code for both nAMD and GA were identified. Of these, 10,140 eyes of 8,324 patients, 12,509 eyes of 11,778 patients, and 4,189 eyes of 3,570 patients were included in Cohorts 1, 2, and 3, respectively. Across all cohorts, mean follow-up time was 2.4 years. Mean age was 81.4 years and 68% were female. Bevacizumab was the most utilized anti-VEGF agent at index across all cohorts. Mean anti-VEGF treatment intervals for Cohorts 1, 2, 3 were 8.09, 7.47, 8.27 weeks, respectively. Baseline VA was worse than 20/200 in 31.2%, 29.1% and 34.5% of patient eyes, respectively. After 6 years of follow-up, median VA dropped by -9, -5, and -9 ETDRS letters (Figure 1). Retinal vasculitis was observed in 0.02%, 0.06% and 0.02% of eyes and ischemic optic neuropathy in 0.2%, 0.3% and 0.2%, respectively over a mean follow-up period of 2.4, 2,3, and 2.9 years, respectively.

Conclusions : This study highlights the divergence in real-world outcomes of anti-VEGF treatment in patients with simultaneously diagnosed GA and nAMD from established clinical study and real-world findings in patients with nAMD alone.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

 

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