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. 2015 Jan;8(1):3-13.
doi: 10.1177/1756285614560733.

Towards the implementation of 'no evidence of disease activity' in multiple sclerosis treatment: the multiple sclerosis decision model

Affiliations

Towards the implementation of 'no evidence of disease activity' in multiple sclerosis treatment: the multiple sclerosis decision model

Martin Stangel et al. Ther Adv Neurol Disord. 2015 Jan.

Abstract

Objective: The introduction of new and potent therapies for the treatment of relapsing remitting multiple sclerosis (MS) has increased the desire for therapeutic success. There is growing doubt that the mere reduction of relapse rate, Expanded Disability Status Scale (EDSS) progression and magnetic resonance imaging (MRI) markers are exclusive and appropriate factors to monitor the new aim of 'no evidence of disease activity' (NEDA). However, there is no generally accepted definition so far.

Methods: To achieve the therapeutic aim of NEDA, a panel of MS experts searched the available literature on clinical and paraclinical outcomes to propose a test battery that is sensitive to detect disease activity in an everyday clinical setting.

Results: The panel proposed to include, besides relapse rate, disability progression and MRI, neuropsychological outcome measures such as cognitive status, fatigue, depression and quality of life. To standardize the examinations in an economic and schematic way, a multifactorial model [multiple sclerosis decision model (MSDM)] that includes the domains 'relapse', 'disability progression', 'MRI', and 'neuropsychology' is proposed. The scheme reflects the complexity of the disease even in the early stages when scales such as the EDSS are not able to distinguish low levels of progression.

Conclusion: The MSDM aims to support early treatment decisions and uncover timely treatment failure. Prospective investigations are required to prove that such a disease-monitoring concept leads to an early and effective silencing of disease activity.

Keywords: disease activity; disease monitoring; magnetic resonance imaging; multiple sclerosis; neuropsychology.

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Conflict of interest statement

Conflict of interest statement: The authors have received honoraria for lecturing, consultation, and support for research from the following companies: MS: Biogen Idec GmbH, Baxter Deutschland GmbH, Bayer Vital GmbH, CSL Behring GmbH, Genzyme, Grifols, Merck-Serono GmbH, Novartis Pharma GmbH, Sanofi Aventis Deutschland GmbH and Teva GmbH. IKP: Actelion, Bayer Pharma AG, Biogen Idec, Genzyme, Merck Serono, Novartis and TEVA. BK: Biogen Idec GmbH, Bayer Vital GmbH, Genzyme, Merck-Serono GmbH, Novartis Pharma GmbH, Sanofi Aventis Deutschland GmbH and Teva GmbH

CL: Biogen Idec GmbH, Bayer Vital GmbH, Genzyme, Merck-Serono GmbH, Novartis Pharma GmbH, Sanofi Aventis Deutschland GmbH und Teva GmbH. BCK: Bayer Health Care, Biogen Idec, Genzyme/Sanofi Aventis, Grifols, Merck-Serono, Mitsubishi Europe, Novartis, Roche, Talecris and Teva.

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