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Effect of Brolucizumab and Aflibercept on the Maximum Thickness of Pigment Epithelial Detachments and Sub-Retinal Pigment Epithelium Fluid in HAWK and HARRIER.
Khanani, Arshad M; Sadda, Srinivas R; Sarraf, David; Tadayoni, Ramin; Wong, David T; Kempf, Anne-Sophie; Saffar, Insaf; Gedif, Kinfemichael; Chang, Andrew.
Afiliación
  • Khanani AM; Sierra Eye Associates, Reno, Nevada; Reno School of Medicine, University of Nevada, Reno, Nevada. Electronic address: arshad.khanani@gmail.com.
  • Sadda SR; Doheny Eye Institute, University of California, Los Angeles, Los Angeles, California.
  • Sarraf D; Stein Eye Institute, University of California, Los Angeles, Los Angeles, California; Ophthalmology, Greater Los Angeles VA Healthcare Center, Los Angeles, California.
  • Tadayoni R; Department of Ophthalmology, Université Paris Cité, AP-HP, Lariboisière, Saint Louis and Fondation Adolphe de Rothschild Hospitals, Paris, France.
  • Wong DT; Department of Ophthalmology and Vision Sciences, Unity Health Toronto - St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
  • Kempf AS; Novartis Pharma AG, Basel, Switzerland.
  • Saffar I; Novartis Pharma AG, Basel, Switzerland.
  • Gedif K; Novartis Pharma AG, Basel, Switzerland.
  • Chang A; Sydney Retina Clinic, Sydney Eye Hospital, Sydney University, Sydney, New South Wales, Australia.
Ophthalmol Retina ; 2024 Jul 19.
Article en En | MEDLINE | ID: mdl-39033924
ABSTRACT

OBJECTIVE:

To compare the efficacy of brolucizumab and aflibercept treatment in reducing the maximum thickness of pigment epithelial detachments (PEDs) and sub-retinal pigment epithelium (sub-RPE) fluid in patients with neovascular age-related macular degeneration in the HAWK and HARRIER studies.

DESIGN:

HAWK and HARRIER were 96-week, prospective, randomized, double-masked, controlled, multicenter studies.

PARTICIPANTS:

A total of 1775 patients across 11 countries were included in the HAWK study, and 1048 patients across 29 countries were included in the HARRIER study. INTERVENTION After 3 monthly loading doses, brolucizumab-treated eyes received injections every 12 weeks or every 8 weeks if disease activity (DA) was detected. Aflibercept-treated eyes received fixed 8-week dosing. MAIN OUTCOME

MEASURES:

Maximum thickness of PEDs and sub-RPE fluid across the macula were assessed at baseline through week 96 in the brolucizumab- and aflibercept-treated patients and in the patient subgroups with DA at week 16 (matched in terms of injection number and treatment interval).

RESULTS:

At week 96, there were greater mean percentage reductions from baseline in maximum thickness of both PEDs and sub-RPE fluid in brolucizumab-treated patients vs. aflibercept-treated patients (PED 19.7% [n = 336] vs. 11.9% [n = 335] in HAWK; 29.5% [n = 364] vs. 18.3% [n = 361] in HARRIER. Sub-RPE fluid 75.4% vs. 57.3% in HAWK; 86.0% vs. 76.3% in HARRIER). A similar trend in mean percentage reductions was observed in patients with DA at week 16.

CONCLUSIONS:

This analysis shows that brolucizumab achieved greater reductions in PEDs and sub-RPE fluid thickness than aflibercept in HAWK and HARRIER. TRIAL REGISTRATION ClinicalTrials.gov Identifiers NCT02307682 (HAWK) and NCT02434328 (HARRIER). FINANCIAL DISCLOSURE(S) Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Ophthalmol Retina Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Ophthalmol Retina Año: 2024 Tipo del documento: Article