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Optimizing the initial choice and timing of therapy in relapsing-remitting multiple sclerosis

机译:优化复发-缓解型多发性硬化症的初始治疗选择和时机

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摘要

With 12 available US Food and Drug Administration approved medications for the treatment of relapsing multiple sclerosis (MS), choosing an initial therapy is no longer a straightforward task. Each disease-modifying therapy (DMT) has a distinct risk–benefit profile and each patient is an individual. Therefore, the development of a simple algorithm to apply in selecting initial therapy is not feasible. Instead, the prescribing physician must consider many factors related to the treatments themselves, such as efficacy, safety, and tolerability, while also taking into account a particular patient’s disease characteristics, personal preferences, comorbid illnesses and reproductive plans. The efficacy of each drug may be assessed through clinical trial data, although these data are limited by scarcity of direct comparisons among the different agents and lack of availability of biomarkers to predict an individual patient’s response. Differences in safety profiles help to distinguish the various DMTs and influence selection of agent; both the known safety concerns, which can be addressed with risk mitigation and monitoring strategies, and the potential for yet undiscovered safety issues must be assessed, and an individual patient’s comfort level with the risks and ability to comply with monitoring must be determined. Potential issues related to tolerability, which largely relate to matters of patient personal preference and lifestyle, should also be factored into the decision-making process. With regard to the timing of therapy initiation, it must be acknowledged that long-term benefits of early DMT have not yet been definitively demonstrated. Nonetheless, starting DMT early in the MS disease course has been shown to have a beneficial effect on relapse prevention, and appears to curtail the atrophy and neurodegenerative changes that are now known to begin at disease onset. Although under certain circumstances there are acceptable reasons for deferring treatment, it is generally recommended that DMT is initiated early in the disease course.
机译:在获得美国食品药品监督管理局(FDA)批准的12种治疗复发性多发性硬化症(MS)的药物后,选择初始治疗不再是一件容易的事。每种疾病缓解疗法(DMT)都有独特的风险收益特征,每个患者都是个体。因此,开发用于选择初始疗法的简单算法是不可行的。相反,开处方的医师必须考虑与治疗本身有关的许多因素,例如功效,安全性和耐受性,同时还要考虑特定患者的疾病特征,个人喜好,合并症和生殖计划。每种药物的疗效都可以通过临床试验数据进行评估,尽管这些数据受到不同药物之间直接比较的匮乏以及缺乏可预测单个患者反应的生物标志物的限制。安全配置文件中的差异有助于区分各种DMT并影响代理的选择;必须通过缓解风险和监视策略来解决已知的安全问题,还必须评估尚未发现的安全问题的可能性,并且必须确定患者的舒适度以及风险和遵守监视的能力。与耐受性有关的潜在问题(主要与患者的个人喜好和生活方式有关)也应纳入决策过程。关于开始治疗的时间,必须承认早期DMT的长期益处尚未得到明确证实。尽管如此,已证明在MS病程的早期开始DMT对预防复发具有有益的作用,并且似乎减少了现已开始于疾病发作的萎缩和神经退行性改变。尽管在某些情况下有可接受的推迟治疗的原因,但通常建议在疾病过程的早期开始使用DMT。

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