4.3 Review

Recognizing and treating suboptimally controlled multiple sclerosis: steps toward regaining command

期刊

CURRENT MEDICAL RESEARCH AND OPINION
卷 25, 期 10, 页码 2459-2470

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1185/03007990903158364

关键词

Disease management; Disease progression; Drug therapy; Relapsing-remitting multiple sclerosis; Treatment failure

资金

  1. Teva
  2. Bayer HealthCare
  3. EMD Serono
  4. Biogen Idec
  5. Teva Neuroscience
  6. GlaxoSmithKline
  7. Pfizer

向作者/读者索取更多资源

Objective: The therapies available today for multiple sclerosis (MS) reduce but do not fully control disease activity. The objective of this article is to review the definitions of and treatments for suboptimally controlled MS and highlight the challenges faced by clinicians to increase awareness of recognizing and managing patients with suboptimally controlled MS. Methods: Published literature describing treatment failure, treatment optimization paradigms or algorithms, clinical studies of therapies in patients with suboptimally controlled MS, or case reports of management of patients with suboptimally controlled MS were identified from searches of EMBASE and MEDLINE. This was supplemented with case reports and discussions from an expert panel meeting of MS specialists focused on the diagnosis and treatment of suboptimally controlled MS. Results: Several groups have created recommendations for evaluating suboptimal response to disease- modifying drugs (DMDs) in MS. Currently no robust evidence- based data exist to guide treatment decisions in patients who have suboptimal response to a particular therapy. In the absence of data, several treatment paradigms for suboptimally controlled MS have been proposed using a step therapy or platform therapy approach. Therapy modifications require consideration of diseaseand patient-specific factors while accounting for the risk-benefit profile of the agent(s). Unapproved drugs and combination therapies should be reserved as agents of last resort because of the experimental nature of these treatments. Conclusions: In the absence of evidence-based data, identifying and treating MS patients with suboptimal response to the available platform therapies remains challenging. Developing algorithms able to quantify breakthrough disease activity and suboptimal response to DMDs in individual MS patients remains an important target for the MS community. Consideration should be given for all reasons why a particular DMD may not be working for a given patient and for the use of an individualized step therapy.

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