Department of Ophthalmology, University Medicine Greifswald, Greifswald, Germany.
Department of Ophthalmology and Laboratory for Visual Science, National Centre for Child Health and Development, Tokyo, Japan.
Eye (Lond). 2024 Jun;38(8):1444-1453. doi: 10.1038/s41433-023-02919-9. Epub 2024 Jan 10.
There are no data on pharmacokinetics, pharmacodynamics, and immunogenicity of intravitreal aflibercept in preterm infants with retinopathy of prematurity (ROP). FIREFLEYE compared aflibercept 0.4 mg/eye and laser photocoagulation in infants with acute-phase ROP requiring treatment.
Infants (gestational age ≤32 weeks or birthweight ≤1500 g) with treatment-requiring ROP in ≥1 eye were randomized 2:1 to receive aflibercept 0.4 mg or laser photocoagulation at baseline in this 24-week, randomized, open-label, noninferiority, phase 3 study. Endpoints include concentrations of free and adjusted bound aflibercept in plasma, pharmacokinetic/pharmacodynamic exploration of systemic anti-vascular endothelial growth factor effects, and immunogenicity.
Of 113 treated infants, 75 received aflibercept 0.4 mg per eye at baseline (mean chronological age: 10.4 weeks), mostly bilaterally (71 infants), and with 1 injection/eye (120/146 eyes). Concentrations of free aflibercept were highly variable, with maximum concentration at day 1, declining thereafter. Plasma concentrations of adjusted bound (pharmacologically inactive) aflibercept increased from day 1 to week 4, decreasing up to week 24. Six infants experienced treatment-emergent serious adverse events within 30 days of treatment; aflibercept concentrations were within the range observed in other infants. There was no pattern between free and adjusted bound aflibercept concentrations and blood pressure changes up to week 4. A low-titer (1:30), non-neutralizing, treatment-emergent anti-drug antibody response was reported in 1 infant, though was not clinically relevant.
24-week data suggest intravitreal aflibercept for treatment of acute-phase ROP is not associated with clinically relevant effects on blood pressure, further systemic adverse events, or immunogenicity.
NCT04004208.
尚无关于早产儿视网膜病变(ROP)患者玻璃体内阿柏西普药代动力学、药效学和免疫原性的数据。FIREFLEYE 比较了玻璃体内注射阿柏西普 0.4mg/眼与激光光凝治疗急性期 ROP 的疗效。
本 24 周、随机、开放标签、非劣效性 III 期研究中,对 1 只或多只眼需要治疗的胎龄≤32 周或出生体重≤1500g 的婴儿,以 2:1 的比例随机分配至接受阿柏西普 0.4mg/眼或激光光凝治疗。主要终点包括血浆中游离和结合型阿柏西普的浓度、系统抗血管内皮生长因子作用的药代动力学/药效学研究以及免疫原性。
113 例接受治疗的婴儿中,75 例婴儿每眼接受玻璃体内阿柏西普 0.4mg(平均胎龄:10.4 周),主要为双眼(71 例婴儿),每眼 1 次注射(120/146 眼)。游离阿柏西普的浓度高度可变,第 1 天达到最大浓度,此后下降。血浆中结合型(无药效)阿柏西普的浓度从第 1 天增加到第 4 周,然后直到第 24 周下降。6 例婴儿在治疗后 30 天内发生治疗出现的严重不良事件;阿柏西普的浓度在其他婴儿中观察到的范围内。在第 4 周之前,游离和结合型阿柏西普的浓度与血压变化之间没有规律。1 例婴儿出现低滴度(1:30)、非中和、治疗出现的抗药物抗体反应,但无临床意义。
24 周的数据表明,玻璃体内注射阿柏西普治疗急性期 ROP 与血压无临床相关影响、无其他全身不良事件或免疫原性无关。
NCT04004208