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Randomized study of interferon beta-1a, low-dose azathioprine, and low-dose corticosteroids in multiple sclerosis
E. Havrdová, R. Zivadinov, J. Krásenský, M.G. Dwyer, I. Nováková, O. Doležal, V. Tichá, L. Dušek, E. Houžvičková, J.L. Cox, N. Bergsland, S. Hussein, A. Svobodník, Z. Seidl, M. Vaněčková, D. Horáková
Language English Country Great Britain
Document type Research Support, Non-U.S. Gov't, Randomized Controlled Trial
NLK
ProQuest Central
from 1998-01-01 to 2015-12-31
SAGE Publications Journals
from 1999-01-01 to 2015-12-31
Health & Medicine (ProQuest)
from 1998-01-01 to 2015-12-31
Family Health Database (ProQuest)
from 1998-01-01 to 2015-12-31
- MeSH
- Administration, Oral MeSH
- Atrophy MeSH
- Azathioprine administration & dosage adverse effects MeSH
- Time Factors MeSH
- Double-Blind Method MeSH
- Adrenal Cortex Hormones administration & dosage adverse effects MeSH
- Immunologic Factors administration & dosage adverse effects MeSH
- Immunosuppressive Agents administration & dosage adverse effects MeSH
- Injections, Intramuscular MeSH
- Interferon-beta administration & dosage adverse effects MeSH
- Drug Therapy, Combination MeSH
- Humans MeSH
- Magnetic Resonance Imaging MeSH
- Brain pathology MeSH
- Disability Evaluation MeSH
- Prednisone administration & dosage adverse effects MeSH
- Disease Progression MeSH
- Prospective Studies MeSH
- Recurrence MeSH
- Multiple Sclerosis, Relapsing-Remitting diagnosis drug therapy MeSH
- Drug Administration Schedule MeSH
- Treatment Outcome MeSH
- Check Tag
- Humans MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
BACKGROUND: Studies evaluating interferon beta (IFNbeta) for multiple sclerosis (MS) showed only partial efficacy. In many patients, IFNbeta does not halt relapses or disability progression. One strategy to potentially enhance efficacy is to combine IFNbeta with classical immunosuppressive agents, such as azathioprine (AZA) or corticosteroids, commonly used for other autoimmune disorders. OBJECTIVE: The Avonex-Steroids-Azathioprine study was placebo-controlled trial and evaluated efficacy of IFNbeta-1a alone and combined with low-dose AZA alone or low-dose AZA and low-dose corticosteroids as initial therapy. METHODS: A total of 181 patients with relapsing-remitting MS (RRMS) were randomized to receive IFNbeta-1a 30 microg intramuscularly (IM) once weekly, IFNbeta-1a 30 microg IM once weekly plus AZA 50 mg orally once daily, or IFNbeta-1a 30 microg IM once weekly plus AZA 50 mg orally once daily plus prednisone 10 mg orally every other day. The primary end point was annualized relapse rate (ARR) at 2 years. Patients were eligible for enrollment in a 3-year extension. RESULTS: At 2 years, adjusted ARR was 1.05 for IFNbeta-1a, 0.91 for IFNbeta-1a plus AZA, and 0.73 for combination. The cumulative probability of sustained disability progression was 16.8% for IFNbeta-1a, 20.7% for IFNbeta-1a plus AZA, and 17.5% for combination. There were no statistically significant differences among groups for either measure at 2 and 5 years. Percent T2 lesion volume change at 2 years was significantly lower for combination (+14.5%) versus IFNbeta-1a alone (+30.3%, P < 0.05). Groups had similar safety profiles. CONCLUSION: In IFNbeta-naive patients with early active RRMS, combination treatment did not show superiority over IFNbeta-1a monotherapy.
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- $a Randomized study of interferon beta-1a, low-dose azathioprine, and low-dose corticosteroids in multiple sclerosis / $c E. Havrdová, R. Zivadinov, J. Krásenský, M.G. Dwyer, I. Nováková, O. Doležal, V. Tichá, L. Dušek, E. Houžvičková, J.L. Cox, N. Bergsland, S. Hussein, A. Svobodník, Z. Seidl, M. Vaněčková, D. Horáková
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- $a Department of Neurology, Charles University in Prague, First Faculty of Medicine, Prague, Czech Republic. eva.havrdova@gmail.com
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- $a BACKGROUND: Studies evaluating interferon beta (IFNbeta) for multiple sclerosis (MS) showed only partial efficacy. In many patients, IFNbeta does not halt relapses or disability progression. One strategy to potentially enhance efficacy is to combine IFNbeta with classical immunosuppressive agents, such as azathioprine (AZA) or corticosteroids, commonly used for other autoimmune disorders. OBJECTIVE: The Avonex-Steroids-Azathioprine study was placebo-controlled trial and evaluated efficacy of IFNbeta-1a alone and combined with low-dose AZA alone or low-dose AZA and low-dose corticosteroids as initial therapy. METHODS: A total of 181 patients with relapsing-remitting MS (RRMS) were randomized to receive IFNbeta-1a 30 microg intramuscularly (IM) once weekly, IFNbeta-1a 30 microg IM once weekly plus AZA 50 mg orally once daily, or IFNbeta-1a 30 microg IM once weekly plus AZA 50 mg orally once daily plus prednisone 10 mg orally every other day. The primary end point was annualized relapse rate (ARR) at 2 years. Patients were eligible for enrollment in a 3-year extension. RESULTS: At 2 years, adjusted ARR was 1.05 for IFNbeta-1a, 0.91 for IFNbeta-1a plus AZA, and 0.73 for combination. The cumulative probability of sustained disability progression was 16.8% for IFNbeta-1a, 20.7% for IFNbeta-1a plus AZA, and 17.5% for combination. There were no statistically significant differences among groups for either measure at 2 and 5 years. Percent T2 lesion volume change at 2 years was significantly lower for combination (+14.5%) versus IFNbeta-1a alone (+30.3%, P < 0.05). Groups had similar safety profiles. CONCLUSION: In IFNbeta-naive patients with early active RRMS, combination treatment did not show superiority over IFNbeta-1a monotherapy.
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