1,721,019 research outputs found

    From pro-re-nata to fixed-interval regimen: evolving real-world treatment paradigms in anti-VEGF therapy for neovascular AMD

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    Objective: To evaluate the impact of evolving treatment paradigms for neovascular age-related macular degeneration (nAMD) by comparing outcomes between two patient cohorts treated with different anti-vascular endothelial growth factor (anti-VEGF) regimens over a decade apart. Methods: This retrospective cohort study included 200 treatment-naive nAMD patients divided into two cohorts. Cohort 1 (2009–2010) was treated with a pro re nata (PRN) regimen, involving three initial monthly injections followed by as-needed treatments based on monthly monitoring. Cohort 2 (2019–2021) received a fixed-interval regimen, consisting of three initial monthly injections followed by bimonthly maintenance doses. Primary outcomes included changes in best corrected visual acuity (BCVA) and central retinal thickness (CRT) at 12 months. Secondary outcomes included the number of injections, follow-up visits, and adherence to treatment schedules. Results: Cohort 2 demonstrated significantly greater improvement in BCVA (+5.5 vs −2.0 ETDRS letters, p < 0.001) and CRT reduction (−101.7 vs −26.5 μm, p < 0.001) compared to Cohort 1. Patients in Cohort 2 received more injections (7.7 vs 4.8, p < 0.001) but required fewer monitoring visits (3.2 vs 5.1, p < 0.001). Adherence to treatment schedules was markedly higher in Cohort 2 (78% vs 0%, p < 0.001). Conclusions: The transition from a PRN to a fixed-interval anti-VEGF regimen significantly improved visual and anatomical outcomes in nAMD patients. Fixed-interval regimens not only enhanced treatment efficacy but also optimized resource utilization, suggesting a superior approach for managing nAMD in a real-world clinical setting

    Extended duration of VEGF inhibition with aflibercept 8 mg: the role of reduced ocular clearance

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    Key messages: What is known • Anti-VEGF therapy is the cornerstone of neovascular AMD treatment, but frequent intravitreal injections are required due to the short half-life and rapid ocular clearance of these agents. What is new • The newly available 8 mg aflibercept formulation exhibits a 34.4% slower ocular clearance compared to the standard 2 mg dose, exceeding predictions based on a simple dose increase. • Pharmacokinetic modeling demonstrates that this reduced clearance extends VEGF suppression duration up to 20 weeks, aligning with clinical outcomes from the PULSAR trial. • The enhanced durability of aflibercept 8 mg appears to be driven by formulation differences, increased viscosity, and altered intravitreal distribution dynamics, offering the potential for extended treatment intervals
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