Should we stay or should we go? Recent insights on drug discontinuation in multiple sclerosis.

Q2 Medicine
Anne Mrochen, Sven G Meuth, Steffen Pfeuffer
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Abstract

Background: The decision to discontinue disease-modifying therapies (DMTs) in patients with multiple sclerosis (PwMS) is a critical clinical challenge. Historically, DMTs were discontinued due to side effects, treatment limitations, or progression to secondary progressive MS. However, advancements in MS therapies, particularly high-efficacy DMTs (HE-DMTs) and the increased knowledge on disease courses and phenotypes have resulted in more personalized treatment approaches and introduced discussion on scheduled DMT discontinuation. This review explores the current evidence on DMT discontinuation, focusing on its implications for aging populations and the interplay between cardiovascular diseases (CVD) and MS.

Current evidence and interplay with cvd: Randomized trials such as DISCOMS and DOT-MS have provided insights into discontinuing DMTs in stable patients. In summary, both randomized clinical trials highlight the risk of disease reactivation following treatment discontinuation. Due to the limited sample size, neither study was able to conduct subgroup analyses based on age groups. Additionally, DOT-MS was terminated prematurely, direct comparisons with other studies should be avoided. While older studies and observational data (e.g., OFSEP) have shown relapse risks associated with discontinuation, particularly for drugs like natalizumab and fingolimod, there is limited data on HE-DMT discontinuation outcomes. Comorbidities, particularly CVDs, further complicate decisions regarding the continuation of DMTs in older adults. MS patients bear a higher burden of CVD, which is also associated with unfavorable disease courses. While optimizing cardiovascular risk profiles appears advisable, it remains unclear whether DMTs themselves have a positive impact on CVDs.

Conclusion: Given the complexities associated with discontinuing DMTs in MS patients, it is essential to balance the avoidance of polypharmacy with the potential risks of disease reactivation and the impact of comorbidities, especially CVDs, on disease progression. The interplay between MS and CVD highlights the importance of a holistic risk assessment when considering DMT discontinuation.

我们该走还是该留?多发性硬化症药物停药的最新见解。
背景:决定停止多发性硬化症(PwMS)患者的疾病改善治疗(DMTs)是一个关键的临床挑战。从历史上看,由于副作用、治疗限制或进展为继发性进展性MS而停用DMT,然而,MS治疗的进步,特别是高效DMT (he -DMT)以及对疾病病程和表型的了解的增加,导致了更个性化的治疗方法,并引入了关于DMT预定停药的讨论。本综述探讨了DMT停药的现有证据,重点关注其对老龄化人群的影响以及心血管疾病(CVD)与ms之间的相互作用。目前的证据和与CVD的相互作用:随机试验,如DISCOMS和DOT-MS,为稳定患者停药提供了新的见解。总之,两项随机临床试验都强调了停药后疾病复发的风险。由于样本量有限,两项研究都无法进行基于年龄组的亚组分析。此外,DOT-MS过早终止,应避免与其他研究直接比较。虽然较早的研究和观察性数据(如OFSEP)显示停药与复发风险相关,特别是对natalizumab和fingolimod等药物,但关于HE-DMT停药结果的数据有限。合并症,特别是心血管疾病,使老年人继续接受dmt的决定进一步复杂化。MS患者有较高的CVD负担,这也与不利的病程有关。虽然优化心血管风险概况似乎是可取的,但目前尚不清楚dmt本身是否对心血管疾病有积极影响。结论:鉴于多发性硬化症患者停用dmt的复杂性,有必要在避免多药治疗与疾病再激活的潜在风险以及合并症(尤其是心血管疾病)对疾病进展的影响之间取得平衡。MS和CVD之间的相互作用强调了在考虑停用DMT时进行全面风险评估的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.40
自引率
0.00%
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审稿时长
14 weeks
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