Heterogeneity in response to interferon beta in patients with multiple sclerosis: a 3-year monthly imaging study
- PMID: 19001157
- DOI: 10.1001/archneur.66.1.noc80047
Heterogeneity in response to interferon beta in patients with multiple sclerosis: a 3-year monthly imaging study
Abstract
Objectives: To investigate the heterogeneity in magnetic resonance image (MRI) patterns of response to interferon beta across patients with multiple sclerosis or within an individual patient over time.
Design, setting, and patients: Fifteen patients with relapsing-remitting multiple sclerosis underwent monthly MRIs and clinical examinations (6-month pretherapy phase and 36-month therapy phase) and bimonthly neutralizing antibody tests. On each MRI, the total number of contrast-enhancing lesions was noted. Therapy MRI responders were defined as those with a reduction of 60% or more in the total number of contrast-enhancing lesions during each semester of therapy.
Intervention: Subcutaneous administration of interferon beta-1b, 250 microg, every other day for 3 years.
Main outcome measure: Reduction in the number of contrast-enhancing lesions.
Results: Eight patients (53.3%) were MRI responders and 7 (46.7%) were nonresponders. Of those 7, 3 (20.0%) had only an initial optimal reduction of the total number of contrast-enhancing lesions, 2 (13.3%) never reached an optimal response, and 2 (13.3%) had a delayed optimal response. No clear association between neutralizing antibody profile and MRI response was evident.
Conclusions: Multiple MRI evaluations disclose that approximately only half of the patients treated with interferon beta achieve and maintain a full response to the drug over time, although an additional small number of individuals may still restore an optimal response to the drug after an initial failure.
Comment in
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Defining multiple sclerosis treatment response with magnetic resonance imaging: how much activity is too much?Arch Neurol. 2009 Jan;66(1):19-20. doi: 10.1001/archneurol.2008.529. Arch Neurol. 2009. PMID: 19139295 No abstract available.
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