Department of Neurology, Hôpitaux Universitaires de Strasbourg, Strasbourg, France/Clinical Investigation Center, INSERM U1434, Strasbourg, France/Biopathology of Myelin, Neuroprotection and Therapeutic Strategies, INSERM U1119, Strasbourg, France.
Groupe méthode en recherche clinique, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Mult Scler. 2021 Apr;27(5):729-741. doi: 10.1177/1352458520936239. Epub 2020 Jul 9.
Data are needed on long-term effect of natalizumab (NTZ) in relapsing-remitting multiple sclerosis (RRMS).
To evaluate the time of onset of secondary progressive phase in patients with an RRMS treated with NTZ and to investigate predictive factors.
TYSTEN is an observational study. Patients starting NTZ between 2007 and 2012 were included and followed up until October 2018. Relapses, Expanded Disability Status Scale (EDSS) scores, and results of brain magnetic resonance imaging (MRI) were collected each year. Data were used to estimate the cumulative probability of several poor outcomes such as secondary progressive multiple sclerosis (SPMS) conversion, EDSS worsening, EDSS 4.0, and EDSS 6.0.
770 patients were included. The mean follow-up duration was 97 months and the mean time exposure to NTZ was 66 months. At 10 years, the cumulative probability of SPMS was 27.7%. Predictive factors for poor outcomes were a ⩾1-point increase in EDSS score from baseline, new T2 lesion or T1 gadolinium-enhancing lesion, the occurrence of relapse at 1 or 2 years and No Evidence of Disease Activity (NEDA-3; no relapse, no new T2 or T1 gadolinium-enhancing lesions, no progression) was a protective factor.
In our cohort of patients treated with NTZ, poor outcomes were infrequent and are driven by disease activity.
需要了解那他珠单抗(natalizumab,NTZ)治疗复发缓解型多发性硬化(RRMS)的长期疗效数据。
评估 RRMS 患者接受 NTZ 治疗后的继发性进展期发病时间,并探讨预测因素。
TYSTEN 是一项观察性研究。纳入 2007 年至 2012 年期间开始接受 NTZ 治疗的患者,并随访至 2018 年 10 月。每年收集复发、扩展残疾状况量表(Expanded Disability Status Scale,EDSS)评分和脑磁共振成像(magnetic resonance imaging,MRI)结果。使用这些数据来估计几种不良结局(如继发进展型多发性硬化(SPMS)转化、EDSS 恶化、EDSS 4.0 和 EDSS 6.0)的累积概率。
共纳入 770 例患者。中位随访时间为 97 个月,NTZ 中位暴露时间为 66 个月。10 年后,SPMS 的累积概率为 27.7%。不良结局的预测因素包括基线 EDSS 评分增加 ⩾1 分、新的 T2 病变或 T1 钆增强病变、第 1 年或第 2 年复发以及无疾病活动证据(NEDA-3;无复发、无新的 T2 或 T1 钆增强病变、无进展)是保护因素。
在接受 NTZ 治疗的患者队列中,不良结局并不常见,且由疾病活动驱动。