Patient Experience With Anti–Vascular Endothelial Growth Factor (VEGF) Therapy in Neovascular Age-Related Macular Degeneration (nAMD) and Diabetic Macular Edema (DME): A Multinational Survey

Author(s)

Gentile B1, Desco Esteban MC2, Jackson T3, Mastropasqua L4, Tuli R5, Chi GC1, Kotecha A6, Mirt M7, Lewis HB8, Tahir MJ9, Holekamp N10
1Genentech, Inc, South San Francisco, CA, USA, 2Instituto Universitario de Investigación Fisabio Oftalmología, València, Spain, 3King’s College London, London, UK, 4Università degli Studi "G. d'Annunzio" Chieti - Pescara, Chieti CH, Italy, 5Retina Centre of Ottawa, Ottawa, ON, Canada, 6Roche Products Limited, Welwyn Garden City, UK, 7F. Hoffmann-La Roche, Basel, Switzerland, 8ICON plc, Reading, UK, 9ICON plc, Blue Bell, PA, USA, 10Pepose Vision Institute, Chesterfield, MO, USA

OBJECTIVES:

Intravitreal anti–vascular endothelial growth factor (VEGF) therapy is efficacious for neovascular age-related macular degeneration (nAMD) and diabetic macular edema (DME). However, the frequent treatment and monitoring required for optimal real-world outcomes can be burdensome to patients and can impact adherence to treatment. This study aimed to understand patient treatment experience with anti-VEGF standard of care.

METHODS:

A cross-sectional survey was employed comprising de novo questions, patient-reported outcome (PRO) measures and medical chart extraction. Adult patients with nAMD or DME treated with intravitreal anti-VEGF injections for ≥12 months were recruited via 38 clinical sites (6 Canada, 6 France, 4 Italy, 7 Spain, 6 United Kingdom, 9 United States).

RESULTS:

Surveys were completed by 391 patients with nAMD and 183 patients with DME. PRO scores indicated that patients across both conditions had relatively high vision-related functioning and were generally satisfied with their current treatment. Mean number of anti-VEGF injections over 12 months across countries ranged from 6.3–9.7 for nAMD and 4.3–8.0 for DME. Nineteen patients with nAMD (19/391; 5%) and 27 patients with DME (27/183; 15%) missed ≥1 injection or examination visit in the past 12 months. Reported barriers were mainly related to treatment (eg, pain and discomfort during/after anti-VEGF injection), clinic (eg, not having someone to accompany them to appointments) and, to a lesser extent, the COVID-19 pandemic. After treatment, the majority recovered in ≤1 day; however, 24% (139/574) needed >1 day to recover. Impairment in daily activities due to treatment was reported by 45% (258/574) of patients. Among working patients 62% (41/66) reported productivity impairment from absenteeism.

CONCLUSIONS:

Patients reported impairment of daily activities, burden and barriers related to intravitreal anti-VEGF therapy, despite high adherence and treatment satisfaction levels. More durable therapy options, requiring less frequent treatments may be able to reduce treatment-related burden and barriers.

Conference/Value in Health Info

2022-11, ISPOR Europe 2022, Vienna, Austria

Value in Health, Volume 25, Issue 12S (December 2022)

Code

PCR275

Topic

Patient-Centered Research

Topic Subcategory

Adherence, Persistence, & Compliance, Patient-reported Outcomes & Quality of Life Outcomes

Disease

SDC: Sensory System Disorders (Ear, Eye, Dental, Skin)

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