Clowse Megan E B, Wolf Douglas C, Förger Frauke, Cush John J, Golembesky Amanda, Shaughnessy Laura, De Cuyper Dirk, Mahadevan Uma
From Duke University Medical Center, Durham; Union Chimique Belge (UCB) Pharma, Raleigh, North Carolina; Atlanta Gastroenterology Associates, Atlanta, Georgia; Baylor Research Institute and Baylor University Medical Center, Dallas, Texas; University of California San Francisco (UCSF) Center for Colitis and Crohn's Disease, San Francisco, California, USA; Department of Rheumatology, Immunology and Allergology, Inselspital, University of Bern, Bern, Switzerland; UCB Pharma, Brussels, Belgium.M.E. Clowse, MD, Duke University Medical Center; D.C. Wolf, MD, Atlanta Gastroenterology Associates; F. Förger, MD, Department of Rheumatology and Immunology and Allergology, Inselspital, University of Bern; J.J. Cush, MD, Baylor Research Institute and Baylor University Medical Center; A. Golembesky, PhD, UCB Pharma; L. Shaughnessy, PhD, UCB Pharma; D. De Cuyper, MD, UCB Pharma; U. Mahadevan, MD, UCSF Center for Colitis and Crohn's Disease.
J Rheumatol. 2015 Dec;42(12):2270-8. doi: 10.3899/jrheum.140189. Epub 2015 Nov 1.
To provide information on pregnancy outcomes in women receiving certolizumab pegol (CZP).
The UCB Pharma safety database was searched for pregnancies through to September 1, 2014. Reports for maternal and paternal CZP exposure were included and outcomes examined, and data on CZP exposure, pregnancy, comorbidities, and infant events were extracted by 2 independent reviewers. Concomitant medications and disease activity were reviewed for clinical trial patients.
Of 625 reported pregnancies, 372 (59.5%) had known outcomes. Paternal exposure pregnancies (n = 33) reported 27 live births, 4 miscarriages, 1 induced abortion, and 1 stillbirth. Maternal exposure pregnancies (n = 339) reported 254 live births, 52 miscarriages, 32 induced abortions, and 1 stillbirth. Almost all reported pregnancies had exposure to CZP in the first trimester, when organogenesis takes place, and a third of them continued the drug into the second and/or third trimesters. The most frequent indications for maternal CZP use were Crohn disease (192/339) and rheumatic diseases (118/339). Twelve cases of congenital malformation and a single neonatal death were reported.
Analysis of pregnancy outcomes after exposure to CZP supports previous reports, suggesting a lack of harmful effect of maternal CZP exposure on pregnancy outcomes. However, additional data from a larger number of outcomes after exposure and studies including an unexposed comparison group are required to fully evaluate CZP safety and tolerability in pregnancy.
提供关于接受聚乙二醇化赛妥珠单抗(CZP)治疗的女性妊娠结局的信息。
检索优时比制药安全数据库中截至2014年9月1日的妊娠病例。纳入母体和父体暴露于CZP的报告并检查结局,由2名独立审阅者提取关于CZP暴露、妊娠、合并症及婴儿事件的数据。对临床试验患者的伴随用药和疾病活动情况进行了回顾。
在625例报告的妊娠中,372例(59.5%)有已知结局。父体暴露的妊娠(n = 33)报告有27例活产、4例流产、1例人工流产和1例死产。母体暴露的妊娠(n = 339)报告有254例活产、52例流产、32例人工流产和1例死产。几乎所有报告的妊娠在器官形成期的孕早期都暴露于CZP,其中三分之一的患者在孕中期和/或孕晚期继续用药。母体使用CZP最常见的适应证是克罗恩病(192/339)和风湿性疾病(118/339)。报告了12例先天性畸形和1例新生儿死亡。
对暴露于CZP后的妊娠结局分析支持先前的报告,表明母体暴露于CZP对妊娠结局没有有害影响。然而,需要更多暴露后结局的数据以及包括未暴露对照组的研究,以全面评估CZP在妊娠中的安全性和耐受性。