Department of Neurology, Langone Medical Center, New York University, New York, New York, USA.
Departments of Neurology & Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
J Neurol Neurosurg Psychiatry. 2016 Aug;87(8):885-9. doi: 10.1136/jnnp-2015-312940. Epub 2016 Feb 25.
Natalizumab (NTZ), a monoclonal antibody to human α4β1/β7 integrin, is an effective therapy for multiple sclerosis (MS), albeit associated with progressive multifocal leukoencephalopathy (PML). Clinicians have been extending the dose of infusions with a hypothesis of reducing PML risk. The aim of the study is to evaluate the clinical consequences of reducing NTZ frequency of infusion up to 8 weeks 5 days.
A retrospective chart review in 9 MS centres was performed in order to identify patients treated with extended interval dosing (EID) regimens of NTZ. Patients were stratified into 3 groups based on EID NTZ treatment schedule in individual centres: early extended dosing (EED; n=249) every 4 weeks 3 days to 6 weeks 6 days; late extended dosing (LED; n=274) every 7 weeks to 8 weeks 5 days; variable extended dosing (n=382) alternating between EED and LED. These groups were compared with patients on standard interval dosing (SID; n=1093) every 4 weeks.
17% of patients on SID had new T2 lesions compared with 14% in EID (p=0.02); 7% of patients had enhancing T1 lesions in SID compared with 9% in EID (p=0.08); annualised relapse rate was 0.14 in the SID group, and 0.09 in the EID group. No evidence of clinical or radiographic disease activity was observed in 62% of SID and 61% of EID patients (p=0.83). No cases of PML were observed in EID group compared with 4 cases in SID cohort.
Dosing intervals up to 8 weeks 5 days did not diminish effectiveness of NTZ therapy. Further monitoring is ongoing to evaluate if the risk of PML is reduced in patients on EID.
那他珠单抗(NTZ)是一种针对人 α4β1/β7 整联蛋白的单克隆抗体,是治疗多发性硬化症(MS)的有效药物,尽管其与进行性多灶性白质脑病(PML)相关。临床医生一直在通过延长输注剂量来减少 PML 风险。本研究旨在评估将 NTZ 输注频率减少至 8 周 5 天的临床后果。
在 9 个 MS 中心进行了回顾性图表审查,以确定接受延长间隔给药(EID)方案 NTZ 治疗的患者。根据各中心的 EID NTZ 治疗方案,患者分为 3 组:早期延长剂量组(EED;n=249),每 4 周 3 天至 6 周 6 天;晚期延长剂量组(LED;n=274),每 7 周至 8 周 5 天;可变延长剂量组(n=382),EED 和 LED 交替。这些组与每 4 周接受标准间隔给药(SID;n=1093)的患者进行比较。
SID 组中有 17%的患者出现新的 T2 病变,而 EID 组中有 14%(p=0.02);SID 组中有 7%的患者出现增强 T1 病变,而 EID 组中有 9%(p=0.08);SID 组的年复发率为 0.14,EID 组为 0.09。SID 组 62%和 EID 组 61%的患者无临床或影像学疾病活动的证据(p=0.83)。EID 组未观察到 PML 病例,而 SID 队列中有 4 例。
剂量间隔长达 8 周 5 天并未降低 NTZ 治疗的疗效。正在进行进一步监测,以评估 EID 患者的 PML 风险是否降低。