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DOI 10.1038/s41433-023-02919-9

Медицинская библиотека · Eye (London, England) · 2024

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

Stahl Andreas, Azuma Noriyuki, Wu Wei-Chi, Lepore Domenico, Sukgen Emine, Nakanishi Hidehiko, Mazela Jan, Leal Sergio, Pieper Alexander, Schlief Sarah, Eissing Thomas, Turner Kenneth C, Zhao An, Winkler Julia, Höchel Joachim, Köfüncü Evra, Zimmermann Torsten, FIREFLEYE Study Group

СтатьяКлиническое исследование III фазыРандомизированное исследованиеМногоцентровое исследованиеEquivalence TrialПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Stahl Andreas, Azuma Noriyuki, Wu Wei-Chi, Lepore Domenico, Sukgen Emine, Nakanishi Hidehiko, Mazela Jan, Leal Sergio, Pieper Alexander, Schlief Sarah, Eissing Thomas, Turner Kenneth C, Zhao An, Winkler Julia, Höchel Joachim, Köfüncü Evra, Zimmermann Torsten, FIREFLEYE Study Group. Systemic exposure to aflibercept after intravitreal injection in premature neonates with retinopathy of prematurity: results from the FIREFLEYE randomized phase 3 study.. Eye (London, England). 2024. DOI: 10.1038/s41433-023-02919-9.

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