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

被引:4
作者
Stahl, Andreas [1 ]
Azuma, Noriyuki [2 ,3 ]
Wu, Wei-Chi [4 ,5 ]
Lepore, Domenico [6 ]
Sukgen, Emine [7 ]
Nakanishi, Hidehiko [8 ]
Mazela, Jan [9 ]
Leal, Sergio [10 ]
Pieper, Alexander [11 ]
Schlief, Sarah [12 ]
Eissing, Thomas [13 ]
Turner, Kenneth C. [14 ]
Zhao, An [14 ]
Winkler, Julia [15 ]
Hoechel, Joachim [12 ]
Kofuncu, Evra [12 ]
Zimmermann, Torsten [12 ]
机构
[1] Univ Med Greifswald, Dept Ophthalmol, Greifswald, Germany
[2] Natl Ctr Child Hlth & Dev, Dept Ophthalmol & Lab Visual Sci, Tokyo, Japan
[3] Tokyo Med & Dent Univ, Med Res Inst, Dept Dev & Regenerat Biol, Tokyo, Japan
[4] Chang Gung Univ, Linkou Chang Gung Mem Hosp, Dept Ophthalmol, Taoyuan, Taiwan
[5] Chang Gung Univ, Coll Med, Taoyuan, Taiwan
[6] Univ Cattolica Sacro Cuore, A Gemelli Fdn IRCCS, Dept Geriatr & Neurosci, Rome, Italy
[7] Hlth Sci Univ, Adana City Training & Res Hosp, Dept Ophthalmol, Adana, Turkiye
[8] Kitasato Univ, Res & Dev Ctr New Med Frontiers, Dept Adv Med, Div Neonatal Intens Care Med,Sch Med, Sagamihara, Japan
[9] Poznan Univ Med Sci, Dept Neonatol, Poznan, Poland
[10] Bayer Consumer Care AG, Basel, Switzerland
[11] Chrestos Concept GmbH & Co KG, Essen, Germany
[12] Bayer AG, Berlin, Germany
[13] Bayer AG, Leverkusen, Germany
[14] Regeneron Pharmaceut Inc, Tarrytown, NY USA
[15] Occams, Amstelveen, Netherlands
关键词
ENDOTHELIAL GROWTH-FACTOR; VEGF-TRAP; INTRAOCULAR PHARMACOKINETICS; MECHANISMS;
D O I
10.1038/s41433-023-02919-9
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
BackgroundThere 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.MethodsInfants (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.ResultsOf 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.Conclusions24-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.ClinicalTrials.gov IdentifierNCT04004208.
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收藏
页码:1444 / 1453
页数:10
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