From IRCCS Don Gnocchi Foundation (E.P.), Florence; Scientific Institute University Vita-Salute San Raffaele (L.M., V.M., G.C.), Milan; Multiple Sclerosis Study Center (P.A., A.G., M.Z.), ASST Valle Olona, Gallarate Hospital (VA); Department of Neurosciences, Reproductive and Odontostomatological Sciences (R.L., V.B.M.), Federico II University of Naples; Department of Neurosciences (F.R., P.G.), Multiple Sclerosis Centre-Veneto Region (CeSMuV), University Hospital of Padova; Department of Neurology (C.T., D.P., M.T.), University of Bari; Department of Neurology and Psychiatry (C.P., L.D.G.), "La Sapienza" University, Rome; Department of Neurology (P.C.), University of Torino; Department of Medical Sciences and Public Health (E.C., M.G.M.), University of Cagliari; Department of Neurology (C.S.), ASL3 Genovese; Department of Neurology (A.U., A.L.), University of Genova; and Department of NEUROFARBA (L.P., M.G., M.P.A.), University of Florence, Italy.
Neurology. 2018 Mar 6;90(10):e832-e839. doi: 10.1212/WNL.0000000000005068. Epub 2018 Feb 7.
To assess the risk of disease reactivation during pregnancy after natalizumab suspension in women with multiple sclerosis (MS).
Data of all pregnancies occurring between 2009 and 2015 in patients with MS treated with natalizumab and referring to 19 participating sites were collected and compared with those of pregnancies in untreated patients and patients treated with injectable immunomodulatory agents through a 2-factor repeated measures analysis. Predictors of disease activity were assessed through stepwise multivariable logistic regression models.
A total of 92 pregnancies were tracked in 83 women receiving natalizumab. Among these pregnancies, 74 in 70 women resulted in live births, with a postpartum follow-up of at least 1 year, and were compared with 350 previously published pregnancies. Relapse rate during and after pregnancy was higher in women treated with natalizumab ( < 0.001). In multivariable analysis, longer natalizumab washout period was the only predictor of relapse occurrence during pregnancy ( = 0.001). Relapses in the postpartum year were related to relapses during pregnancy ( = 0.019) and early reintroduction of disease-modifying drugs (DMD; = 0.021). Disability progression occurred in 16.2% of patients and was reduced by early reintroduction of DMD ( = 0.024).
Taken as a whole, our findings indicate that the combination of avoiding natalizumab washout and the early resumption of DMD after delivery could be the best option in the perspective of maternal risk. This approach must take into account possible fetal risks that need to be discussed with the mother and require further investigation.
This study provides Class IV evidence that in women with MS, the risk of relapses during pregnancy is higher in those who had been using natalizumab as compared to those who had been using interferon-β or no treatment.
评估多发性硬化症(MS)女性患者使用那他珠单抗注射液停药后怀孕期间疾病再激活的风险。
收集了 2009 年至 2015 年期间在使用那他珠单抗治疗的 MS 患者中发生的所有妊娠数据,并与未接受治疗的患者和接受注射免疫调节剂治疗的患者的妊娠数据进行了比较,比较方法为两因素重复测量分析。通过逐步多变量逻辑回归模型评估疾病活动的预测因素。
共追踪了 83 名接受那他珠单抗治疗的女性的 92 例妊娠。在这些妊娠中,74 例在 70 名女性中分娩,产后随访至少 1 年,并与之前发表的 350 例妊娠进行了比较。接受那他珠单抗治疗的女性在怀孕期间和产后的复发率更高(<0.001)。在多变量分析中,较长的那他珠单抗冲洗期是怀孕期间复发的唯一预测因素(=0.001)。产后一年内的复发与怀孕期间的复发(=0.019)和早期重新引入疾病修正药物(DMD;=0.021)有关。16.2%的患者出现残疾进展,早期重新引入 DMD 可降低残疾进展(=0.024)。
总的来说,我们的研究结果表明,从母体风险的角度来看,避免那他珠单抗冲洗和产后尽早恢复 DMD 的组合可能是最佳选择。这种方法必须考虑到可能需要与母亲讨论的胎儿风险,并需要进一步调查。
本研究提供了 IV 级证据,表明在 MS 女性患者中,与使用干扰素-β或未治疗相比,使用那他珠单抗的患者在怀孕期间复发的风险更高。