Department of Neurology, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.
Department of Neurology, University Hospital and Faculty of Medicine and Dentistry, Palacky University, Olomouc, Czech Republic.
Curr Opin Neurol. 2019 Jun;32(3):365-377. doi: 10.1097/WCO.0000000000000700.
To critically assess the current landscape of disease-modifying agents for multiple sclerosis (MS). Treatment algorithms will be discussed and studies for new agents in late development or recently approved are analyzed in terms of their impact on current treatment strategies.
A real-world study from Wales suggests that early initiation of highly effective therapy may provide more benefit that an escalation approach in relapsing MS. A study from the MSBase dataset found evidence that early treatment with highly effective therapies decreased the risk of developing secondary progressive MS. Ocrelizumab is highly efficacious in relapsing MS and in a group of patients with primary progressive MS. Another CD20 directed mAb, ofatumumab, is in phase 3. A large study examining extended interval dosing of natalizumab in an attempt to decrease the risk of developing progressive multifocal leukoencephalopathy is underway. Cladribine and alemtuzumab may work by immune reconstitution. Siponimod was recently approved by United States Federal Drug Administration for relapsing MS and active secondary progressive MS. Other S1P receptor modulators are being studied in phase 3 trials for relapsing MS. Cladribine received FDA approval as treatment for relapsing and active secondary progressive MS. Autologous hematopoetic stem-cell transplantation may be an option for treatment-refractory MS.
Development of disease-modifying agents in MS continues to be successful. Treatment algorithms need to take new developments into account.
批判性评估多发性硬化症(MS)的疾病修正治疗药物的现状。将讨论治疗方案,并根据对当前治疗策略的影响,分析晚期开发或最近批准的新药物的研究。
来自威尔士的一项真实世界研究表明,在复发型 MS 中,早期开始使用高效疗法可能比升级疗法带来更大的益处。来自 MSBase 数据集的一项研究发现,早期使用高效疗法可降低发展为继发进展型 MS 的风险。奥瑞珠单抗在复发型 MS 和一组原发性进展型 MS 患者中具有高度疗效。另一种靶向 CD20 的 mAb,奥法妥木单抗,处于 3 期研究中。一项大型研究正在评估那他珠单抗的延长间隔给药,以试图降低进展性多灶性白质脑病的风险。克拉屈滨和阿仑单抗可能通过免疫重建发挥作用。西尼莫德最近被美国食品和药物管理局批准用于治疗复发型 MS 和活动性继发进展型 MS。其他 S1P 受体调节剂正在进行 3 期复发型 MS 试验研究。克拉屈滨获得 FDA 批准,用于治疗复发和活动性继发进展型 MS。自体造血干细胞移植可能是治疗难治性 MS 的一种选择。
MS 中的疾病修正治疗药物的开发仍在继续取得成功。治疗方案需要考虑新的发展。