“No evidence of disease activity”: Is it an aspirational therapeutic goal in multiple sclerosis?

dc.contributor.authorMayssam, El Najjar
dc.contributor.authorEid, Cynthia
dc.contributor.authorKhoury, Samia J.
dc.contributor.authorHannoun, S.
dc.contributor.departmentNeurology
dc.contributor.departmentSpecialized Clinical Programs and Services
dc.contributor.departmentNehme and Therese Tohme Multiple Sclerosis (MS) Center
dc.contributor.departmentAbu-Haidar Neuroscience Institute (AHNI)
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:07:38Z
dc.date.available2025-01-24T12:07:38Z
dc.date.issued2020
dc.description.abstract‘No evidence of disease activity’ (NEDA) that has been identified as a potential outcome measure for the evaluation of DMTs effects. The concept has been adopted from other diseases such as cancer where treatment is intended to free the patient from the disease. Disease-free status has been substituted by NEDA in MS, since we are limited when it comes to fully evaluating the underlying disease. In general, NEDA, otherwise termed as NEDA-3, is defined by the lack of disease activity based on the absence of clinical relapses, disability progression with the expanded disability status score (EDSS), and radiological activity. Recently, brain atrophy, a highly predictive marker of disability progression, has been added as a fourth component (NEDA-4). The use of this composite allowed a more comprehensive assessment of the disease activity. Indeed, it has an important role in clinical trials as a secondary outcome in addition to primary endpoints. However, the evidence is insufficient regarding the ability of NEDA to predict future disability and treatment response. Moreover, combining different composites does not eliminate the limitation of each, therefore the use of NEDA in clinical routine is still not implemented. The aim of this review is first to report from the literature the available definitions of NEDA and its different variants, and second, evaluate the importance of its use as a surrogate marker to assess the efficacy of different DMTs. © 2020 Elsevier B.V.
dc.identifier.doihttps://doi.org/10.1016/j.msard.2020.101935
dc.identifier.eid2-s2.0-85077932864
dc.identifier.pmid31951861
dc.identifier.urihttp://hdl.handle.net/10938/31590
dc.language.isoen
dc.publisherElsevier B.V.
dc.relation.ispartofMultiple Sclerosis and Related Disorders
dc.sourceScopus
dc.subjectMagnetic resonance imaging (mri)
dc.subjectMultiple sclerosis
dc.subjectNeda-3
dc.subjectNeda-4
dc.subjectNo evidence of disease activity (neda)
dc.subjectDisease progression
dc.subjectHumans
dc.subjectImmunologic factors
dc.subjectMagnetic resonance imaging
dc.subjectOutcome assessment, health care
dc.subjectSeverity of illness index
dc.subjectAlemtuzumab
dc.subjectFingolimod
dc.subjectNatalizumab
dc.subjectOcrelizumab
dc.subjectPeginterferon beta1a
dc.subjectImmunologic factor
dc.subjectBrain atrophy
dc.subjectDisability
dc.subjectDisease activity
dc.subjectDisease assessment
dc.subjectDisease marker
dc.subjectDrug efficacy
dc.subjectExpanded disability status scale
dc.subjectHuman
dc.subjectMeta analysis
dc.subjectOutcome assessment
dc.subjectPrediction
dc.subjectRadioactivity
dc.subjectRelapse
dc.subjectReview
dc.subjectSystematic review
dc.subjectTreatment response
dc.subjectDiagnostic imaging
dc.subjectDisease exacerbation
dc.subjectNuclear magnetic resonance imaging
dc.subjectPathology
dc.subjectPathophysiology
dc.title“No evidence of disease activity”: Is it an aspirational therapeutic goal in multiple sclerosis?
dc.typeReview

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