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Risk Factors for Meeting Criteria for Switching from Bevacizumab to Aflibercept When Treating Eyes with Diabetic Macular Edema and Visual Acuity of < 20/40.
Jhaveri, Chirag D; Liu, Danni; Maguire, Maureen G; Glassman, Adam R; Grigorian, Ruben A; Jampol, Lee M; Kingsley, Ronald M; MacCumber, Mathew W; Martin, Daniel F; Maturi, Raj K; Velez, Gisela; Sun, Jennifer K.
  • Jhaveri CD; Retina Consultants of Austin and Austin Research Center for Retina, Austin, Texas.
  • Liu D; Jaeb Center for Health Research, Tampa, Florida.
  • Maguire MG; Jaeb Center for Health Research, Tampa, Florida.
  • Glassman AR; Jaeb Center for Health Research, Tampa, Florida. Electronic address: drcrstat2@jaeb.org.
  • Grigorian RA; Joseph E. Humble and Raymond Haik PTRS DBA Eye Association of Northeast Louisiana.
  • Jampol LM; Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
  • Kingsley RM; Dean A. McGee Eye Institute, Oklahoma City, Oklahoma.
  • MacCumber MW; Rush University Medical Center, Department of Ophthalmology, Chicago, Illinois.
  • Martin DF; Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio.
  • Maturi RK; Midwest Eye Institute, and Indiana University School of Medicine, Department of Ophthalmology, Indianapolis, Indiana.
  • Velez G; Valley Eye Physicians and Surgeons, Ayer, Massachusetts.
  • Sun JK; Beetham Eye Institute, Joslin Diabetes Center, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts.
Ophthalmology ; 131(8): 967-974, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38336282
ABSTRACT

PURPOSE:

To identify factors for meeting prespecified criteria for switching from bevacizumab to aflibercept in eyes with center-involved diabetic macular edema (CI-DME) and moderate vision loss initially treated with bevacizumab in DRCR Retina Network protocol AC.

DESIGN:

Post hoc analysis of data from a randomized clinical trial.

PARTICIPANTS:

Two hundred seventy participants with one or both eyes harboring CI-DME with visual acuity (VA) letter score of 69 to 24 (Snellen equivalent, 20/50-20/320).

METHODS:

Eligible eyes were assigned to receive intravitreal aflibercept monotherapy (n = 158) or bevacizumab followed by aflibercept if prespecified criteria for switching were met between 12 weeks and 2 years (n = 154). MAIN OUTCOME

MEASURES:

Meeting switching criteria (1) at any time, (2) at 12 weeks, and (3) after 12 weeks. Associations between meeting the criteria for switching and factors measured at baseline and 12 weeks were evaluated in univariable analyses. Stepwise procedures were used to select variables for multivariable models.

RESULTS:

In the group receiving bevacizumab first, older participants showed a higher risk of meeting the switching criteria at any time, with a hazard ratio (HR) for a 10-year increase in age of 1.32 (95% confidence interval [CI], 1.11-1.58). Male participants or eyes with worse baseline VA were more likely to switch at 12 weeks (for male vs. female odds ratio [OR], 4.84 [95% CI, 1.32-17.81]; 5-letter lower baseline VA OR, 1.30 [95% CI, 1.03-1.63]). Worse 12-week central subfield thickness (CST; 10-µm greater HR, 1.06 [95% CI, 1.04-1.07]) was associated with increased risk of switching after 12 weeks. The mean ± standard deviation improvement in visual acuity after completing the switch to aflibercept was 3.7 ± 4.9 letters compared with the day of switching.

CONCLUSIONS:

The identified factors can be used to refine expectations regarding the likelihood that an eye will meet protocol criteria to switch to aflibercept when treatment is initiated with bevacizumab. Older patients are more likely to be switched. At 12 weeks, thicker CST was predictive of eyes most likely to be switched in the future. 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 Banco de datos: MEDLINE Asunto principal: Proteínas Recombinantes de Fusión / Agudeza Visual / Edema Macular / Inhibidores de la Angiogénesis / Receptores de Factores de Crecimiento Endotelial Vascular / Factor A de Crecimiento Endotelial Vascular / Retinopatía Diabética / Inyecciones Intravítreas / Sustitución de Medicamentos / Bevacizumab Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Recombinantes de Fusión / Agudeza Visual / Edema Macular / Inhibidores de la Angiogénesis / Receptores de Factores de Crecimiento Endotelial Vascular / Factor A de Crecimiento Endotelial Vascular / Retinopatía Diabética / Inyecciones Intravítreas / Sustitución de Medicamentos / Bevacizumab Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article