Paediatric outcomes after maternal nipocalimab for haemolytic disease of the fetus and newborn: an open-label, single-arm study.

IF 3.5 2区 医学 Q1 PEDIATRICS
Derek P de Winter, Kenneth J Moise, Leona E Ling, Dick Oepkes, Eleonor Tiblad, E J T Joanne Verweij, John Smoleniec, Ulrich J Sachs, Gregor Bein, Mark D Kilby, Russell S Miller, Roland Devlieger, Anne Debeer, Jocelyn H Leu, Robert M Nelson, Valerie Smith, Lisa B Schwartz, May Lee Tjoa, Yosuke Komatsu, Shumyla Saeed-Khawaja, Enrico Lopriore
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引用次数: 0

Abstract

Objectives: To describe haemolytic disease outcomes, growth, neurodevelopment and health-related quality of life (HRQoL) through 24 months of life in infants exposed to nipocalimab in pregnancies at high risk of early-onset severe haemolytic disease of the fetus and newborn (EOS-HDFN).

Design: A multicentre, open-label, single-arm trial.

Setting: Centres with expertise in HDFN management.

Patients: Pregnant individuals with previous EOS-HDFN and maternal anti-D titres ≥32 or anti-K titres ≥4.

Interventions: Weekly nipocalimab (30 and/or 45 mg/kg) from 14 to 35 gestational weeks.

Main outcome measures: Infants' cord-blood alloantibody titres at birth, HDFN management, growth through 6 months, neurodevelopment (caregiver-reported Ages and Stages Questionnaire, third edition (ASQ-3)) and HRQoL assessments through 24 months of life.

Results: Of 13 pregnancies, 12 resulted in live births; one fetal loss occurred due to intrauterine transfusion (IUT) complications. A single simple transfusion was administered in one of seven infants delivered after a maternal nipocalimab course without IUTs, where cord blood alloantibody titres were <8. Multiple transfusions (one to seven simple transfusions/infant; one exchange transfusion) were administered to five infants delivered after early nipocalimab discontinuation and IUTs, with cord-blood alloantibody titres ranging from 512 to 32 768. No unusual growth patterns were observed through 6 months. No neurodevelopmental delays were identified through 24 months of life, with mean ASQ-3 domain scores within normal ranges. HRQoL outcomes were positive across physical, emotional, social and cognitive functioning.

Conclusions: Maternal nipocalimab in pregnancies at high risk of EOS-HDFN may reduce adverse neonatal outcomes correlating with low cord-blood alloantibody titres, without affecting growth through 6 months, neurodevelopment or HRQoL through 24 months of life.

Trial registration number: NCT03842189.

孕妇使用尼波卡利单抗治疗胎儿和新生儿溶血性疾病的儿科结局:一项开放标签单臂研究
目的:描述早发性严重溶血性胎儿和新生儿疾病(EOS-HDFN)高危妊娠暴露于尼波卡利单抗的婴儿在24个月内的溶血性疾病结局、生长、神经发育和健康相关生活质量(HRQoL)。设计:一项多中心、开放标签、单臂试验。环境:具有hdf管理专业知识的中心。患者:既往患有eos - hdf且母体抗d效价≥32或抗k效价≥4的孕妇。干预措施:妊娠14至35周,每周一次尼波卡利单抗(30和/或45 mg/kg)。主要结局指标:婴儿出生时脐带血同种异体抗体滴度、hdf管理、6个月的生长、神经发育(护理人员报告的年龄和阶段问卷,第三版(ASQ-3))和24个月的HRQoL评估。结果:13例妊娠,12例活产;1例胎儿因宫内输血(IUT)并发症而流产。结论:高危妊娠孕妇的尼波卡利单抗可降低与低脐带血同种抗体滴度相关的新生儿不良结局,不影响6个月的生长,不影响24个月的神经发育或HRQoL。试验注册号:NCT03842189。
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来源期刊
CiteScore
9.00
自引率
4.50%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Archives of Disease in Childhood is an international peer review journal that aims to keep paediatricians and others up to date with advances in the diagnosis and treatment of childhood diseases as well as advocacy issues such as child protection. It focuses on all aspects of child health and disease from the perinatal period (in the Fetal and Neonatal edition) through to adolescence. ADC includes original research reports, commentaries, reviews of clinical and policy issues, and evidence reports. Areas covered include: community child health, public health, epidemiology, acute paediatrics, advocacy, and ethics.
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