Suppr超能文献

早产儿视网膜病变经玻璃体腔内注射后脉络膜血管生成抑制剂阿柏西普的全身暴露:FIREFLEYE 随机 3 期研究结果。

Systemic exposure to aflibercept after intravitreal injection in premature neonates with retinopathy of prematurity: results from the FIREFLEYE randomized phase 3 study.

机构信息

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.

出版信息

Eye (Lond). 2024 Jun;38(8):1444-1453. doi: 10.1038/s41433-023-02919-9. Epub 2024 Jan 10.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

GOV IDENTIFIER

NCT04004208.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

政府标识符

NCT04004208

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/263f/11126565/903bcd029afb/41433_2023_2919_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验