June 2022
Volume 63, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2022
Discontinuation, switching, and other long-term real-world treatment patterns among patients with diabetic macular edema initiating anti-VEGF: 6-year follow-up using the IRIS® Registry
Author Affiliations & Notes
  • Eunice Kim
    Genentech Inc, South San Francisco, California, United States
  • Vince Garmo
    Genentech Inc, South San Francisco, California, United States
  • David Tabano
    Genentech Inc, South San Francisco, California, United States
  • Blanche Kuo
    Case Western Reserve University, Cleveland, Ohio, United States
  • Theodore Leng
    Verana Health, San Francisco, California, United States
  • Meghan Hatfield
    Verana Health, San Francisco, California, United States
  • Andrew LaPrise
    Verana Health, San Francisco, California, United States
  • Rishi P Singh
    Cleveland Clinic Cole Eye Institute, Cleveland, Ohio, United States
  • Footnotes
    Commercial Relationships   Eunice Kim Genentech, Code E (Employment); Vince Garmo Genentech, Code E (Employment); David Tabano Genentech, Code E (Employment); Blanche Kuo None; Theodore Leng Graybug, Alcon, Nanoscope Therapeutics, Verana Health, Astellas, Genentech, Regeneron, Code C (Consultant/Contractor), Targeted Therapy Technologies, Kodiak, Code F (Financial Support); Meghan Hatfield None; Andrew LaPrise None; Rishi Singh Novartis, Genentech, Regeneron, Alcon, Bausch and Lomb, 41 Gyroscope, Code C (Consultant/Contractor), Aerie, Apellis, Graybug, Code F (Financial Support)
  • Footnotes
    Support  F. Hoffmann-La Roche Ltd. (Basel, Switzerland) provided support for the study and participated in the study design; conducting the study; and data collection, management, and interpretation.
Investigative Ophthalmology & Visual Science June 2022, Vol.63, 2523 – F0249. doi:
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      Eunice Kim, Vince Garmo, David Tabano, Blanche Kuo, Theodore Leng, Meghan Hatfield, Andrew LaPrise, Rishi P Singh; Discontinuation, switching, and other long-term real-world treatment patterns among patients with diabetic macular edema initiating anti-VEGF: 6-year follow-up using the IRIS® Registry. Invest. Ophthalmol. Vis. Sci. 2022;63(7):2523 – F0249.

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

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Abstract

Purpose : This study aimed to characterize long-term treatment patterns among patients with diabetic macular edema (DME) from a large ophthalmology registry.

Methods : A retrospective analysis was performed among treatment-naïve DME patients (no prior anti-vascular endothelial growth factor (anti-VEGF) intravitreal therapy [IVT] in the past 12 months) initiating IVT from 1/1/2015-12/31/2019 using de-identified electronic medical records (IRIS® Registry). Anti-VEGF agent utilization patterns, including agent type, switches (defined as ≥3 consecutive injections of a different anti-VEGF agent from the original agent), and discontinuations (defined as no anti-VEGF IVT for ≥12 months). Results were stratified by baseline visual acuity (VA) and initial anti-VEGF agent including on-label (ranibizumab and aflibercept) and off-label agent (bevacizumab).

Results : Of 190,345 eyes (147,687 patients), 147,336 eyes (77%) received only 1 anti-VEGF agent over a mean follow-up of 2.3 years, with bevacizumab being the most commonly used agent (53% of eyes). Bevacizumab use decreased by a mean of 5.6% each year and on-label agent use increased by a mean of 6.9% each year (Figure 1). 15% of eyes switched anti-VEGF agents after a mean of 53 weeks, of which 74% switched from bevacizumab to an on-label agent. 52% of eyes discontinued anti-VEGF treatment after a mean of 24 weeks, of which 33% reinitiated after a mean of 91 weeks. Rates of discontinuation, switching, and reinitiation were mostly similar regardless of baseline VA, though discontinuation with no reinitiation of IVT during follow-up was highest in patients with VA ≤20/200 at baseline (Figure 2).

Conclusions : Although a majority of patients with DME discontinue IVT therapy after a mean of 6 months, a third reinitiated. 58% patients initially received bevacizumab, but its use decreased over time with an increased use of on-label agents. Reasons for switching and discontinuation should be further explored.

This abstract was presented at the 2022 ARVO Annual Meeting, held in Denver, CO, May 1-4, 2022, and virtually.

 

 

*Mean follow-up times were 2.4, 2.4, 2.3, 2.1, and 2.1 years for patients with baseline VA ≥20/25, <20/25 to 20/40, <20/40 to 20/80, <20/80 to >20/200 and ≤20/200, respectively.

*Mean follow-up times were 2.4, 2.4, 2.3, 2.1, and 2.1 years for patients with baseline VA ≥20/25, <20/25 to 20/40, <20/40 to 20/80, <20/80 to >20/200 and ≤20/200, respectively.

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