This paper is only available as a PDF. To read, Please Download here.
Summary
There is now a consensus that early treatment of patients with relapsing–remitting
multiple sclerosis is desirable, mainly because early treatment may delay the accumulation
of disability, but also because disease-modifying treatments seem to be more effective
when started early in the course of the disease. In particular, all current first-line
disease-modifying treatments have also been shown to be effective in treating clinically
isolated syndrome. The evidence for this comes from extensive experience in randomised
controlled Phase III clinical trials. While many patients presenting a clinically
isolated syndrome are at high risk of experiencing a second attack, early treatment
with all disease-modifying treatments has been shown to delay conversion to clinically
definite multiple sclerosis when compared to late treatment. Some of these trials
have completed five years of follow-up. While the evidence for early intervention
is stronger than ever, it is worthwhile to consider its relevance to everyday clinical
practice. In particular, it is important to determine which patients are the best
candidates for early therapy and to evaluate the anticipated risks and benefits of
choosing a given therapy for a given patient.
Keywords
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Journal of the Neurological SciencesAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- Recommended diagnostic criteria for multiple sclerosis: guidelines from the International Panel on the diagnosis of multiple sclerosis.Ann Neurol. 2001; 50: 121-127
- Application of the new McDonald criteria to patients with clinically isolated syndromes suggestive of multiple sclerosis.Ann Neurol. 2002; 52: 47-53
- New diagnostic criteria for multiple sclerosis: application in first demyelinating episode.Neurology. 2003; 60: 27-30
- MRI criteria for MS in patients with clinically isolated syndromes.Neurology. 2010; 74: 427-434
- Acute axonal damage in multiple sclerosis is most extensive in early disease stages and decreases over time.Brain. 2002; 125: 2202-2212
- Multiple sclerosis.Lancet. 2008; 372: 1502-1517
- Acute axonal injury in multiple sclerosis. Correlation with demyelination and inflammation.Brain. 2000; 123: 1174-1183
- Axonal transection in the lesions of multiple sclerosis.N Engl J Med. 1998; 338: 278-285
- Onset and underpinnings of white matter atrophy at the very early stage of multiple sclerosis–a two-year longitudinal MRI/MRSI study of corpus callosum.Mult Scler. 2007; 13: 41-51
- Atrophy mainly affects the limbic system and the deep grey matter at the first stage of multiple sclerosis.J Neurol Neurosurg Psychiatry. 2010; 81: 690-695
- Detection of ventricular enlargement in patients at the earliest clinical stage of MS.Neurology. 2000; 54: 1689-1691
- Progressive ventricular enlargement in patients with clinically isolated syndromes is associated with the early development of multiple sclerosis.J Neurol Neurosurg Psychiatry. 2002; 73: 141-147
- Brain atrophy and lesion load measures over 1 year relate to clinical status after 6 years in patients with clinically isolated syndromes.J Neurol Neurosurg Psychiatry. 2010; 81: 204-208
- Assessing brain atrophy rates in a large population of untreated multiple sclerosis subtypes.Neurology. 2010; 74: 1868-1876
- The natural history of multiple sclerosis: a geographically based study. I. Clinical course and disability.Brain. 1989; 112: 133-146
- The natural history of multiple sclerosis: a geographically based study. 2. Predictive value of the early clinical course.Brain. 1989; 112: 1419-1428
- Disability and T2 MRI lesions: a 20-year follow-up of patients with relapse onset of multiple sclerosis.Brain. 2008; 131: 808-817
- Baseline MRI predicts future attacks and disability in clinically isolated syndromes.Neurology. 2006; 67: 968-972
- Subgroups of the BENEFIT study: risk of developing MS and treatment effect of interferon beta-1b.J Neurol. 2008; 255: 480-487
- MRI characteristics are predictive for CDMS in monofocal, but not in multifocal patients with a clinically isolated syndrome.BMC Neurol. 2009; 9: 19
- Early clinical predictors and progression of irreversible disability in multiple sclerosis: an amnesic process.Brain. 2003; 126: 770-782
- Clinical and demographic predictors of long-term disability in patients with relapsing–remitting multiple sclerosis: a systematic review.Arch Neurol. 2006; 63: 1686-1691
- The natural history of multiple sclerosis: a geographically based study. 3. Multivariate analysis of predictive factors and models of outcome.Brain. 1991; 114: 1045-1056
- Intramuscular interferon beta-1a therapy initiated during a first demyelinating event in multiple sclerosis. CHAMPS Study Group.N Engl J Med. 2000; 343: 898-904
- Effect of early interferon treatment on conversion to definite multiple sclerosis: a randomised study.Lancet. 2001; 357: 1576-1582
- Treatment with interferon beta-1b delays conversion to clinically definite and McDonald MS in patients with clinically isolated syndromes.Neurology. 2006; 67: 1242-1249
- Effect of glatiramer acetate on conversion to clinically definite multiple sclerosis in patients with clinically isolated syndrome (PreCISe study): a randomised, double-blind, placebo-controlled trial.Lancet. 2009; 374: 1503-1511
- Shifting the paradigm toward earlier treatment of multiple sclerosis with interferon beta.Clin Ther. 2009; 31: 1142-1157
- The controlled high risk Avonex multiple sclerosis trial (CHAMPS Study).J Neuroophthalmol. 2001; 21: 292-295
- Treatment with glatiramer acetate protects axons in patients with clinically isolated syndromes: evidence from the PreCISe trial.Mult Scler. 2008; 14: S10
- Proton MR spectroscopy in multiple sclerosis.Neuroimaging Clin N Am. 2000; 10 (ix–x.): 789-798
- Benefit of early treatment with glatiramer acetate: MRI results from the 5-year prospectively planned follow up in patients with clinically isolated syndrome enrolled in the PreCISe study.Mult Scler. 2010; 16: S349
- Effect of early versus delayed interferon beta-1b treatment on disability after a first clinical event suggestive of multiple sclerosis: a 3-year follow-up analysis of the BENEFIT study.Lancet. 2007; 370: 389-397
- Long-term effect of early treatment with interferon beta-1b after a first clinical event suggestive of multiple sclerosis: 5-year active treatment extension of the phase 3 BENEFIT trial.Lancet Neurol. 2009; 8: 987-997
- IM interferon beta-1a delays definite multiple sclerosis 5 years after a first demyelinating event.Neurology. 2006; 66: 678-684
- CHAMPIONS: 10-year follow-up after a clinically isolated syndrome in patients at high risk for developing multiple sclerosis.Multiple Sclerosis. 2009; 15: P466
European Medicines Agency. Refusal of the marketing authorisation for Movectro (cladribine) 2010 [cited; Available from: http://www.ema.europa.eu/docs/en_GB/document_library/Summary_of_opinion_-_Initial_authorisation/human/001197/WC500097016.pdf
- Efficacy of intramuscular interferon beta-1a in patients with clinically isolated syndrome: analysis of subgroups based on new risk criteria.Mult Scler. 2009; 15: 728-734
- Discrepancies in the interpretation of clinical symptoms and signs in the diagnosis of multiple sclerosis. A proposal for standardization.Mult Scler. 2005; 11: 227-231
- [Update on current care guidelines: diagnostics, treatment and rehabilitation of multiple sclerosis].Duodecim. 2010; 126: 199-200
Article info
Identification
Copyright
© 2011 Elsevier B.V. Published by Elsevier Inc. All rights reserved.