Maximilian Einsiedler, Chiara Zecca, Lisa Hofer, Pascal Benkert, Cathrine Axfors, Francesca Bedussi, Alessandro Ceschi, Giulio Disanto, Jannis Müller, Johanna Oechtering, Johannes Lorscheider, Edoardo Galli, Bettina Fischer-Barnicol, Marcus D'Souza, Sabine Anna Schaedelin, Aleksandra Maleska Maceski, Robert Hoepner, Andrew Chan, Cristina Granziera, Sebastian Finkener, Lutz Achtnichts, Caroline Pot, Renaud A Du Pasquier, Marjolaine Uginet, Patrice H Lalive, Stefanie Mueller, Patrick Roth, Ludwig Kappos, Claudio Gobbi, Tobias J Derfuss, David Leppert, Jens Kuhle, Özgür Yaldizli
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We aim to describe therapy regimens, clinical and MRI disease activity, and serum neurofilament light chain (sNfL) levels in all pregnancies observed between 2012 and 2023 among participants of the Swiss MS cohort.</p><p><strong>Methods: </strong>We assessed the treatment strategies during pregnancy and 1 year postpartum in all included pregnancies. We compared pregnancies continuously exposed to high-efficacy disease-modifying therapies (cHET: anti-CD20 monoclonal antibodies (aCD20) and natalizumab [NTZ]) with those where other therapeutic regimens (OTRs) were used. Disease activity was assessed by occurrence of relapses or new or enlarging T2w lesions (neT2Ls), as well as sNfL Z scores. We estimated odds ratios adjusted for age, disease duration, Expanded Disability Status Scale (EDSS) score, and previous relapse rate using generalized estimating equation (GEE) models for the relapse endpoint and using Firth logistic regression for MRI activity. sNfL Z scores were compared between treatment categories at sampling using GEE models.</p><p><strong>Results: </strong>We analyzed 123 pregnancies in 93 women (median age [interquartile range {IQR}] 32.2 years [29.3, 35.7]; EDSS score [IQR] 1.5 [1.0, 2.0]). The last disease-modifying therapy (DMT) before birth was NTZ in 29 (23.5%) and aCD20 in 25 (20.3%) pregnancies; of those, 3 and 24 were exposed until birth, respectively (cHET). Fingolimod was the last treatment before birth in 25 pregnancies (20.3%), stopped in all before or after confirmation of pregnancy. Other DMTs were used in 39 pregnancies (31.7%); 5 remained untreated. Compared with cHET, patients with pregnancies under OTRs had higher proportions of relapses (34.4% vs 13.0%; n = 113, OR 4.52, 95% CI [1.35-15.11], <i>p</i> = 0.0142) and neT2Ls (40.9% vs 3.8%; n = 91, OR 9.15, 95% CI [2.14-85.21], <i>p</i> = 0.0013). sNfL Z scores during pregnancy and postpartum were higher in patients untreated at sampling compared with patients under high-efficacy DMT (HET) (+0.43 Z score units, 95% CI [0.05-0.81], <i>p</i> = 0.0255). No serious adverse events were observed.</p><p><strong>Discussion: </strong>Treatment strategies for pregnant patients with MS were heterogeneous, and continuous exposure to HET showed superior efficacy against acute disease activity compared with other DMTs or no treatment. Further studies are needed to confirm these results and assess maternal and fetal longer term outcomes.</p>","PeriodicalId":19136,"journal":{"name":"Neurology. 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We aim to describe therapy regimens, clinical and MRI disease activity, and serum neurofilament light chain (sNfL) levels in all pregnancies observed between 2012 and 2023 among participants of the Swiss MS cohort.</p><p><strong>Methods: </strong>We assessed the treatment strategies during pregnancy and 1 year postpartum in all included pregnancies. We compared pregnancies continuously exposed to high-efficacy disease-modifying therapies (cHET: anti-CD20 monoclonal antibodies (aCD20) and natalizumab [NTZ]) with those where other therapeutic regimens (OTRs) were used. Disease activity was assessed by occurrence of relapses or new or enlarging T2w lesions (neT2Ls), as well as sNfL Z scores. We estimated odds ratios adjusted for age, disease duration, Expanded Disability Status Scale (EDSS) score, and previous relapse rate using generalized estimating equation (GEE) models for the relapse endpoint and using Firth logistic regression for MRI activity. sNfL Z scores were compared between treatment categories at sampling using GEE models.</p><p><strong>Results: </strong>We analyzed 123 pregnancies in 93 women (median age [interquartile range {IQR}] 32.2 years [29.3, 35.7]; EDSS score [IQR] 1.5 [1.0, 2.0]). The last disease-modifying therapy (DMT) before birth was NTZ in 29 (23.5%) and aCD20 in 25 (20.3%) pregnancies; of those, 3 and 24 were exposed until birth, respectively (cHET). Fingolimod was the last treatment before birth in 25 pregnancies (20.3%), stopped in all before or after confirmation of pregnancy. Other DMTs were used in 39 pregnancies (31.7%); 5 remained untreated. 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引用次数: 0
摘要
背景和目的:在妊娠和产后管理多发性硬化症(MS)是一个治疗挑战。我们的目标是描述在2012年至2023年期间观察到的瑞士MS队列参与者中所有妊娠的治疗方案、临床和MRI疾病活动性和血清神经丝轻链(sNfL)水平。方法:我们评估了所有纳入研究的妊娠期间和产后1年的治疗策略。我们比较了持续暴露于高效疾病改善疗法(cHET:抗cd20单克隆抗体(aCD20)和natalizumab [NTZ])的妊娠与使用其他治疗方案(OTRs)的妊娠。通过复发、新发或扩大T2w病变(neT2Ls)的发生以及sNfL Z评分来评估疾病活动性。我们使用复发终点的广义估计方程(GEE)模型和MRI活动的Firth逻辑回归来估计经年龄、病程、扩展残疾状态量表(EDSS)评分和既往复发率调整后的比值比。采用GEE模型比较采样时不同治疗类别的sNfL Z评分。结果:我们分析了93名妇女的123例妊娠(中位年龄[四分位数间距{IQR}] 32.2岁[29.3,35.7];EDSS评分[IQR] 1.5[1.0, 2.0])。产前最后一次疾病改善治疗(DMT)为NTZ 29例(23.5%),aCD20 25例(20.3%);其中,分别有3名和24名一直接触到出生(见图)。芬戈莫德是25例(20.3%)孕妇出生前的最后一种治疗方法,在确认怀孕之前或之后全部停止。39例(31.7%)妊娠使用其他dmt;5人未接受治疗。与cHET相比,OTRs妊娠患者的复发比例更高(34.4% vs 13.0%;n = 113, OR 4.52, 95% CI [1.35-15.11], p = 0.0142)和neT2Ls (40.9% vs 3.8%;n = 91, OR 9.15, 95% CI [2.14-85.21], p = 0.0013)。与高效DMT (HET)患者相比,未接受治疗的患者妊娠和产后sNfL Z评分较高(+0.43 Z评分单位,95% CI [0.05-0.81], p = 0.0255)。未观察到严重不良事件。讨论:妊娠MS患者的治疗策略是异质性的,与其他dmt或不治疗相比,持续暴露于HET对急性疾病活动的疗效更佳。需要进一步的研究来证实这些结果,并评估母体和胎儿的长期预后。
Treatment Strategies and Disease Activity During Pregnancy and Postpartum: Real-World Data From the Swiss Multiple Sclerosis Cohort.
Backgrounds and objectives: Managing multiple sclerosis (MS) during pregnancy and postpartum is a therapeutic challenge. We aim to describe therapy regimens, clinical and MRI disease activity, and serum neurofilament light chain (sNfL) levels in all pregnancies observed between 2012 and 2023 among participants of the Swiss MS cohort.
Methods: We assessed the treatment strategies during pregnancy and 1 year postpartum in all included pregnancies. We compared pregnancies continuously exposed to high-efficacy disease-modifying therapies (cHET: anti-CD20 monoclonal antibodies (aCD20) and natalizumab [NTZ]) with those where other therapeutic regimens (OTRs) were used. Disease activity was assessed by occurrence of relapses or new or enlarging T2w lesions (neT2Ls), as well as sNfL Z scores. We estimated odds ratios adjusted for age, disease duration, Expanded Disability Status Scale (EDSS) score, and previous relapse rate using generalized estimating equation (GEE) models for the relapse endpoint and using Firth logistic regression for MRI activity. sNfL Z scores were compared between treatment categories at sampling using GEE models.
Results: We analyzed 123 pregnancies in 93 women (median age [interquartile range {IQR}] 32.2 years [29.3, 35.7]; EDSS score [IQR] 1.5 [1.0, 2.0]). The last disease-modifying therapy (DMT) before birth was NTZ in 29 (23.5%) and aCD20 in 25 (20.3%) pregnancies; of those, 3 and 24 were exposed until birth, respectively (cHET). Fingolimod was the last treatment before birth in 25 pregnancies (20.3%), stopped in all before or after confirmation of pregnancy. Other DMTs were used in 39 pregnancies (31.7%); 5 remained untreated. Compared with cHET, patients with pregnancies under OTRs had higher proportions of relapses (34.4% vs 13.0%; n = 113, OR 4.52, 95% CI [1.35-15.11], p = 0.0142) and neT2Ls (40.9% vs 3.8%; n = 91, OR 9.15, 95% CI [2.14-85.21], p = 0.0013). sNfL Z scores during pregnancy and postpartum were higher in patients untreated at sampling compared with patients under high-efficacy DMT (HET) (+0.43 Z score units, 95% CI [0.05-0.81], p = 0.0255). No serious adverse events were observed.
Discussion: Treatment strategies for pregnant patients with MS were heterogeneous, and continuous exposure to HET showed superior efficacy against acute disease activity compared with other DMTs or no treatment. Further studies are needed to confirm these results and assess maternal and fetal longer term outcomes.
期刊介绍:
Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.