Cohan Stanley L, Edwards Keith, Lucas Lindsay, Gervasi-Follmar Tiffany, O'Connor Judy, Siuta Jessica, Kamath Vineetha, Garten Lore, Chen Chiayi, Thomas James, Smoot Kyle, Kresa-Reahl Kiren, Spinelli Kateri J
Providence Multiple Sclerosis Center, Providence Brain and Spine Institute, USA.
Multiple Sclerosis Center of Northeastern New York, USA.
Mult Scler J Exp Transl Clin. 2019 Jan 16;5(1):2055217318824618. doi: 10.1177/2055217318824618. eCollection 2019 Jan-Mar.
Natalizumab is an effective treatment for relapsing multiple sclerosis. Return of disease activity upon natalizumab discontinuance creates the need for follow-up therapeutic strategies.
To assess the efficacy of teriflunomide following natalizumab discontinuance in relapsing multiple sclerosis patients.
Clinically stable relapsing multiple sclerosis patients completing 12 or more consecutive months of natalizumab, testing positive for anti-John Cunningham virus antibody, started teriflunomide 14 mg/day, 28 ± 7 days after their final natalizumab infusion. Physical examination, Expanded Disability Status Scale, laboratory assessments, and brain magnetic resonance imaging were performed at screening and multiple follow-up visits.
Fifty-five patients were enrolled in the study. The proportion of patients relapse-free was 0.94, restricted mean time to first gadolinium-enhancing lesion was 10.9 months and time to 3-month sustained disability worsening was 11.8 months. The mean number of new or enlarging T2 lesions per patient at 12 months was 0.42. Exploratory analyses revealed an annualized relapse rate of 0.08, and a proportion of patients with no evidence of disease activity of 0.68. Forty-seven patients (85.5%) reported adverse events, 95% of which were mild to moderate.
Teriflunomide therapy initiated without natalizumab washout resulted in a low rate of return of disease activity. Clinicians may consider this a worthwhile strategy when transitioning clinically stable patients off natalizumab to another therapy.ClinicalTrials.gov Identifier: NCT01970410.
那他珠单抗是复发型多发性硬化症的有效治疗药物。停用那他珠单抗后疾病活动的复发使得需要后续的治疗策略。
评估在复发型多发性硬化症患者停用那他珠单抗后特立氟胺的疗效。
临床稳定的复发型多发性硬化症患者连续使用那他珠单抗12个月或更长时间,抗约翰·坎宁安病毒抗体检测呈阳性,在最后一次输注那他珠单抗后28±7天开始服用特立氟胺14毫克/天。在筛查和多次随访时进行体格检查、扩展残疾状态量表评估、实验室检查和脑磁共振成像。
55名患者纳入研究。无复发患者比例为0.94,首次钆增强病灶的受限平均时间为10.9个月,3个月持续残疾恶化时间为11.8个月。12个月时每位患者新出现或扩大的T2病灶平均数量为0.42。探索性分析显示年化复发率为0.08,无疾病活动证据的患者比例为0.68。47名患者(85.5%)报告了不良事件,其中95%为轻度至中度。
未进行那他珠单抗洗脱就开始特立氟胺治疗导致疾病活动复发率较低。当将临床稳定的患者从那他珠单抗转换为另一种治疗时,临床医生可认为这是一种值得采用的策略。临床试验注册号:NCT01970410。