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

被引:1
|
作者
Wu, Lihteh [1 ]
Bordon, Arnaldo F. [2 ]
Charles, Martin [3 ]
Rodriguez, Francisco J. [4 ]
Lee, JinKyung [5 ]
Machewitz, Tobias [5 ]
Mueller, Margarete [5 ]
Gay, Gabriela Del Carmen [6 ]
Fromow-Guerra, Jans [7 ]
机构
[1] Asociados Macula Vitreo & Retina Costa Rica, Calle 24, San Jose 10102, Costa Rica
[2] Hosp Oftalmol Sorocaba, R Nabek Shiroma 210, BR-18031060 Sorocaba, SP, Brazil
[3] Ctr Oftalmol Dr Charles, 841,C116 ABA Riobamba, Buenos Aires, DF, Argentina
[4] Univ Rosario, Sch Med, Fdn Oftalmol, Cl 50 13-50, Bogota 110231, Colombia
[5] Bayer AG, D-13342 Berlin, Germany
[6] Bayer SA, Doctor Ricardo Gutierrez 3652,B1605EHD Munro, Buenos Aires, DF, Argentina
[7] Macula Retina Consultores, Calle Sur 132, Mexico City 01120, DF, Mexico
关键词
Macula; Neovascularization; Vision; Clinical trial; OUTCOMES;
D O I
10.1186/s40942-022-00425-w
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
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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页数:10
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