3.8 Article

Intravitreal aflibercept for the treatment of patients with neovascular age-related macular degeneration in routine clinical practice in Latin America: the AQUILA study

Journal

Publisher

BMC
DOI: 10.1186/s40942-022-00425-w

Keywords

Macula; Neovascularization; Vision; Clinical trial

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Funding

  1. Bayer AG, Germany

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AQUILA is the first study to evaluate the use of IVT-AFL in routine clinical practice in Latin America. The results showed that nAMD patients who received regular IVT-AFL treatment had significant improvements in visual acuity.
Background: AQUILA (NCT03470103) was a prospective, observational, 12-month cohort study evaluating treatment patterns, clinical effectiveness, and safety of intravitreal aflibercept (IVT-AFL) in patients from Latin America with neovascular age-related macular degeneration (nAMD). Methods: Treatment-naive and previously treated (switching to IVT-AFL) patients (aged >= 55 years) were enrolled from March 2018, with a primary completion date of September 2020, from Argentina, Colombia, Costa Rica, and Mexico. Patients received IVT-AFL in a routine clinical practice setting. Results: Of 274 patients in the full analysis set, 201 were treatment-naive and 73 had received previous treatment. The mean +/- standard deviation number of IVT-AFL injections received by month 12 was 4.2 +/- 1.9 (treatment-naive) and 5.2 +/- 2.7 (previously treated). The median duration from diagnosis to IVT-AFL treatment was 1.2 months (treatment-naive) and 19.5 months (previously treated). Mean best-corrected visual acuity (BCVA) (Early Treatment Diabetic Retinopathy Study [ETDRS] letters) improved from baseline to month 12 by + 5.2 +/- 18.3 (treatment-naive; baseline: 48.2 +/- 23.5) and + 3.1 +/- 15.3 letters (previously treated; baseline: 47.7 +/- 21.4). Conclusion: AQUILA is the first study to assess the use of IVT-AFL in routine clinical practice in Latin America. Mean BCVA and other visual acuity outcomes improved in both treatment groups, despite many patients not receiving the IVT-AFL label-recommended regimen of three initial monthly doses, or seven or more injections in 12 months. Patients who did receive the label-recommended number of injections had numerically greater improvements in visual acuity outcomes. Patients with nAMD treated regularly and more frequently with IVT-AFL, therefore, have the potential to achieve outcomes consistent with those observed in interventional studies.

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