Hellwig Kerstin, Tilson Hugh H, Thiel Sandra, Ball Kathryn, Seebeck Joerg, Danten Muriel, Dubois Nancy, Sabidó Meritxell
Neurological Clinic, University of Bochum, Bochum, Germany.
School of Global Public Health, University of North Carolina, Chapel Hill, NC.
Neurol Neuroimmunol Neuroinflamm. 2025 Sep;12(5):e200438. doi: 10.1212/NXI.0000000000200438. Epub 2025 Jun 30.
With its use being contradicted during pregnancy, limited information exists concerning pregnancy and infant outcomes on exposure to cladribine tablets before or during pregnancy in women with multiple sclerosis (MS). In this study, we assess cumulative pregnancy exposure to cladribine tablets and prevalence of pregnancy and infant outcomes in women with MS exposed during pregnancy or within 6 months before conception and pregnancies fathered by men with MS exposed within 6 months before conception.
MAPLE-MS, a 10-year enhanced pharmacovigilance program, uses a global patient safety database to assess pregnancy outcomes potentially associated with cladribine tablets exposure in MS. Data collection began after the first approval of cladribine tablets (August 22, 2017). The primary outcome is the prevalence of major congenital anomalies (MCAs) in offspring. Secondary outcomes include other pregnancy outcomes (live birth, elective termination, spontaneous abortion, ectopic pregnancy, and stillbirth).
In this Year 7 interim analysis, of 383 pregnancies analyzed, 336 (87.7%) involved maternal exposure to cladribine tablets and 47 (12.3%) were associated with paternal exposure. In the maternal exposure group, MCA prevalence (excluding genetic anomalies) in pregnancies with known outcomes was 1.1% (95% confidence interval [CI] 0.0-6.7; an atrial septal defect). Prevalence of live births in the maternal exposure group was 57.3% (95% CI 49.5-64.8). Secondary outcomes in the maternal exposure group were elective terminations (21.0% [95% CI 15.3-28.1]), spontaneous abortions (20.4% [95% CI 14.8-27.4]), and ectopic pregnancies (1.3% [95% CI 0.1-4.8]). In the paternal exposure group, no cases of MCA were observed in live births with known outcomes. Prevalence of live births was 81.3% (95% CI 56.2-94.2). Spontaneous abortions occurred in 12.5% (95% CI 2.2-37.3) and stillbirths in 6.3% (95% CI 0.0-30.3) of cases.
Results are limited by the small number of pregnancies with known outcomes. Of pregnancies with known outcomes, the majority resulted in live births, with low frequencies of elective terminations and stillbirths reported. Since 2017, a single MCA (atrial septal defect) has been reported to the global patients' safety database. The results align with published estimates from the general population and MS patient cohorts.
由于孕期使用氯法拉滨片存在争议,关于患有多发性硬化症(MS)的女性在妊娠前或妊娠期接触氯法拉滨片后的妊娠及婴儿结局的信息有限。在本研究中,我们评估了妊娠期间或受孕前6个月内接触氯法拉滨片的MS女性的累积妊娠暴露情况以及妊娠和婴儿结局的发生率,以及受孕前6个月内接触过氯法拉滨片的男性所孕育的妊娠情况。
MAPLE-MS是一项为期10年的强化药物警戒计划,利用全球患者安全数据库评估MS患者接触氯法拉滨片后可能相关的妊娠结局。数据收集于氯法拉滨片首次获批后开始(2017年8月22日)。主要结局是后代中重大先天性异常(MCA)的发生率。次要结局包括其他妊娠结局(活产、选择性终止妊娠、自然流产、异位妊娠和死产)。
在这项第7年的中期分析中,在分析的383例妊娠中,336例(87.7%)涉及母亲接触氯法拉滨片,47例(12.3%)与父亲接触有关。在母亲接触组中,已知结局的妊娠中MCA发生率(不包括遗传异常)为1.1%(95%置信区间[CI]0.0 - 6.7;房间隔缺损)。母亲接触组的活产率为57.3%(95%CI 49.5 - 64.8)。母亲接触组的次要结局为选择性终止妊娠(21.0%[95%CI 15.3 - 28.1])、自然流产(20.4%[95%CI 14.8 - 27.4])和异位妊娠(1.3%[95%CI 0.1 - 4.8])。在父亲接触组中,已知结局的活产中未观察到MCA病例。活产率为81.3%(95%CI 56.2 - 94.2)。自然流产发生率为12.5%(95%CI 2.2 - 37.3),死产发生率为6.3%(9%CI 0.0 - 30.3)。
结果受到已知结局妊娠数量较少的限制。在已知结局的妊娠中,大多数为活产,报告的选择性终止妊娠和死产频率较低。自2017年以来,全球患者安全数据库报告了1例MCA(房间隔缺损)。结果与一般人群和MS患者队列的已发表估计一致。