Department of Surgical and Medical Sciences Advanced Technologies GF Ingrassia, University of Catania, Catania, Italy.
Neurology Unit, Fondazione Istituto San Raffaele G. Giglio di Cefalù, Cefalu, Sicily, Italy.
J Neurol Neurosurg Psychiatry. 2020 Dec;91(12):1297-1303. doi: 10.1136/jnnp-2020-323472. Epub 2020 Oct 14.
Natalizumab (NTZ) is one of the most effective treatment options for multiple sclerosis (MS) treatment. Our study aimed to evaluate the effectiveness of NTZ when administered according to the extended dosing strategy compared with standard 4-weekly administration in a large Italian MS population.
This retrospective multicentre study included patients with relapsing-remitting MS (RR-MS) who received NTZ administrations between the 1 June 2012 and the 15 May 2018 and were followed by the 'Italian MS Register'. All patients with MS were stratified into two groups based on NTZ administration schedule: standard interval dosing (SID) patients who received infusions on average from 28 to 32 days (median 30) and extended interval dosing (EID) including patients who have been infused with interval between 33 and 49 days (median 43). Clinical data were assessed at baseline (before starting NTZ), after 12 (T1) and 24 months (T2) of treatment.
Out of 5231 patients with RR-MS screened, 2092 (mean age 43.2±12.0, 60.6% women) were enrolled. A total of 1254 (59.9%) received NTZ according to SID, and 838 (40.1%) according to EID. At 12 and 24 months, no differences in terms of annualised relapse rate and disability status were found between the two groups. Progression index and confirmed disability worsening were similar between the two groups.
The use of NTZ with an extended interval schedule showed similar effectiveness compared with SID. Unchanged clinical efficacy of EID schedule may raise the question of a possible advantage in terms of tolerability and safety.
那他珠单抗(NTZ)是治疗多发性硬化症(MS)最有效的治疗方法之一。我们的研究旨在评估在意大利大型 MS 人群中,与标准的 4 周给药方案相比,根据扩展给药方案给予 NTZ 的有效性。
这项回顾性多中心研究纳入了在 2012 年 6 月 1 日至 2018 年 5 月 15 日期间接受 NTZ 治疗的复发缓解型多发性硬化症(RR-MS)患者,并通过“意大利多发性硬化症登记处”进行随访。所有 MS 患者均根据 NTZ 给药方案分为两组:标准间隔给药(SID)患者,其输注间隔平均为 28-32 天(中位数 30 天);延长间隔给药(EID)组包括输注间隔为 33-49 天(中位数 43 天)的患者。临床数据在基线(开始使用 NTZ 前)、治疗 12 个月(T1)和 24 个月(T2)时进行评估。
在筛选的 5231 例 RR-MS 患者中,有 2092 例(平均年龄 43.2±12.0,60.6%为女性)被纳入研究。共有 1254 例(59.9%)患者接受 SID 治疗,838 例(40.1%)患者接受 EID 治疗。在 12 个月和 24 个月时,两组患者的年复发率和残疾状况无差异。两组间进展指数和确诊残疾恶化情况相似。
使用延长间隔方案的 NTZ 显示出与 SID 相似的有效性。EID 方案的临床疗效不变可能引发关于其在耐受性和安全性方面可能具有优势的问题。