One-Year and 18-Month Outcomes in nAMD Patient Eyes Switched to Brolucizumab Alone versus to Brolucizumab Alternating with Other Anti-VEGF Agents

Objective: Retrospective, real-world study to evaluate visual acuity (VA), anti-vascular endothelial growth factor (anti-VEGF) injection intervals, and central macular thickness (CMT) in neovascular age-related macular degeneration (nAMD) eyes switched to brolucizumab only or to brolucizumab alterna...

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Veröffentlicht in:Clinical ophthalmology (Auckland, N.Z.) N.Z.), 2023-11, Vol.17, p.3601-3611
Hauptverfasser: Coney, Joseph M, McCoy, Jasmyne E, Sinha, Samriddhi Buxy, Sonbolian, Nina, Zhou, Lujia, Hull, Thomas P, Lewis, Shawn A, Miller, David G, Novak, Michael A, Pendergast, Scott D, Pham, Hang, Platt, Sean M, Rao, Llewelyn J, Schartman, Jerome P, Singerman, Lawrence J, Donkor, Richard, Fink, Margaret, Zubricky, Ryan, Karcher, Helene
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Sprache:eng
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Zusammenfassung:Objective: Retrospective, real-world study to evaluate visual acuity (VA), anti-vascular endothelial growth factor (anti-VEGF) injection intervals, and central macular thickness (CMT) in neovascular age-related macular degeneration (nAMD) eyes switched to brolucizumab only or to brolucizumab alternating with another anti-VEGF. Methods: The overall study population comprised eyes that were given [greater than or equal to] 1 brolucizumab injection between 1 October 2019 and 30 November 2021. The brolucizumab-only (BRO) cohort consisted of prior anti-VEGF-treated eyes treated exclusively with [greater than or equal to] 3 brolucizumab injections over [greater than or equal to] 12 or [greater than or equal to] 18 months; the alternating brolucizumab (ALT) cohort comprised prior anti-VEGF-treated eyes treated with [greater than or equal to] 2 brolucizumab injections and [greater than or equal to] 1 other anti-VEGF over [greater than or equal to] 12 or [greater than or equal to] 18 months. Results: A total of 482 eyes received[greater than or equal to] >1 brolucizumab injection during the study period. Mean VA changes from baseline were -1.1 [+ or -] 15.1 letters (BRO cohort; n = 174) and 1.3 [+ or -] 13.0 letters (ALT cohort; n = 47) at Month 12, and 0.0 [+ or -] 13.5 letters (BRO cohort; n = 95) and -7.3 [+ or -] 17.2 letters (ALT cohort; n = 29) at Month 18. Mean changes in injection intervals were +26.9 [+ or -] 48.1 days (BRO cohort) and +11.1 [+ or -] 17.3 days (ALT cohort) at Month 12 and +36.3 [+ or -] 52.3 days (BRO cohort) and +14.0 [+ or -] 19.9 days (ALT cohort) at Month 18. Mean changes in CMT were -35.2 [+ or -] 108.1 pm (BRO cohort) and -31.5 [+ or -] 91.2 [ILLUSTRATION OMITTED] m (ALT cohort) at Month 12 and -38.9 [+ or -] 75.0 [micro]m (BRO cohort) and -9.0 [+ or -] 59.9 [micro]m (ALT cohort) at Month 18. Intraocular inflammation-related adverse events were recorded in 22/482 (4.6%) eyes. Conclusion: Treatment with either brolucizumab alone or brolucizumab alternating with another anti-VEGF can preserve vision, reduce CMT, and extend anti-VEGF injection intervals in patients with nAMD. Keywords: alternating anti-VEGF treatments, brolucizumab, neovascular age-related macular degeneration, wet age-related macular degeneration, 12-month outcomes, 18-month outcomes
ISSN:1177-5483
1177-5467
1177-5483
DOI:10.2147/OPTH.S432957