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UK AMD/DR EMR REPORT IX: comparative effectiveness of predominantly as needed (PRN) ranibizumab versus continuous aflibercept in UK clinical practice.
Lee, Aaron Y; Lee, Cecilia S; Egan, Catherine A; Bailey, Clare; Johnston, Robert L; Natha, Salim; Hamilton, Robin; Khan, Rehna; Al-Husainy, Sahar; Brand, Christopher; Akerele, Toks; Mckibbin, Martin; Downey, Louise; Tufail, Adnan.
Afiliação
  • Lee AY; Department of Ophthalmology, University of Washington, Seattle, Washington, USA.
  • Lee CS; Moorfields Eye Hospital NHS Foundation Trust, London, UK.
  • Egan CA; Department of Ophthalmology, University of Washington, Seattle, Washington, USA.
  • Bailey C; UCL Institute of Ophthalmology, London, UK.
  • Johnston RL; The NIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation TrustLondonUK, London, UK.
  • Natha S; Bristol Eye Hospital, Bristol, UK.
  • Hamilton R; Gloucestershire Hospitals NHS Foundation Trust, Cheltenham, UK.
  • Khan R; Wrightington, Wigan and Leigh NHS Foundation Trust, Lancashire, UK.
  • Al-Husainy S; UCL Institute of Ophthalmology, London, UK.
  • Brand C; Calderdale and Huddersfield NHS Foundation Trust, Huddersfield, UK.
  • Akerele T; Heart of England NHS Foundation Trust, Solihull, UK.
  • Mckibbin M; Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Downey L; Hinchingbrooke Health Care NHS Trust, Huntingdon, UK.
  • Tufail A; Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Br J Ophthalmol ; 101(12): 1683-1688, 2017 12.
Article em En | MEDLINE | ID: mdl-28478396
ABSTRACT

AIMS:

To compare the effectiveness of continuous aflibercept versus pro re nata (PRN) ranibizumab therapy for neovascular age-related macular degeneration (nAMD).

METHODS:

Multicentre, national electronic medical record (EMR) study on treatment naive nAMD eyes undergoing PRN ranibizumab or continuous (fixed or treat and extend (F/TE)) aflibercept from 21 UK hospitals. Anonymised data were extracted, and eyes were matched on age, gender, starting visual acuity (VA) and year of starting treatment. Primary outcome was change in vision at 1 year.

RESULTS:

1884 eyes (942 eyes in each group) were included. At year 1, patients on PRN ranibizumab gained 1.6 ETDRS (Early Treatment Diabetic Retinopathy Study) letters (95% CI 0.5 to 2.7, p=0.004), while patients on F/TE aflibercept gained 6.1 letters (95% CI 5.1 to 7.1, p=2.2e-16). Change in vision at 1 year of the F/TE aflibercept group was 4.1 letters higher (95% CI 2.5 to 5.8, p=1.3e-06) compared with the PRN ranibizumab group after adjusting for age, starting VA, gender and year of starting therapy. The F/TE aflibercept group had significantly more injections compared with the PRN ranibizumab group (7.0 vs 5.8, p<2.2e-16), but required less clinic visits than the PRN ranibizumab group (10.8 vs 9.0, p<2.2e-16). Cost-effectiveness analysis showed an incremental cost-effectiveness ratio of 58 047.14 GBP/quality-adjusted life year for continuous aflibercept over PRN ranibizumab.

CONCLUSION:

Aflibercept achieved greater VA gains at 1 year than ranibizumab. The observed VA differences are small and likely to be related to more frequent treatment with aflibercept, suggesting that ranibizumab should also be delivered by F/TE posology.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes de Fusão / Acuidade Visual / Receptores de Fatores de Crescimento do Endotélio Vascular / Degeneração Macular Exsudativa / Ranibizumab Tipo de estudo: Clinical_trials / Evaluation_studies Limite: Aged / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Br J Ophthalmol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes de Fusão / Acuidade Visual / Receptores de Fatores de Crescimento do Endotélio Vascular / Degeneração Macular Exsudativa / Ranibizumab Tipo de estudo: Clinical_trials / Evaluation_studies Limite: Aged / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Br J Ophthalmol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos