Journal
MULTIPLE SCLEROSIS JOURNAL
Volume 11, Issue 5, Pages 573-582Publisher
SAGE PUBLICATIONS LTD
DOI: 10.1191/1352458505ms1210oa
Keywords
brain atrophy; breakthrough disease; combination therapy; cyclophosphamide; cytotoxic agents; eosinophilia; eosinophils; glucocorticoids; IFN beta; IL-4; methylprednisolone; mitoxantrone; MRI; MS; natalizumab = antegren = tysabri; randomized clinical trial; RRMS; treatment failure
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Funding
- NINDS NIH HHS [1 K23 NS02 117-01] Funding Source: Medline
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Objective: To evaluate the efficacy and safety of combination therapy with pulse cyclophosphamide given with methylprednisolone ( MP) and interferon beta (IFN beta)-1a in multiple sclerosis (MS) patients with active disease during IFN beta monotherapy. Methods: This was a randomized, single-blind, parallel-group, multicenter trial in MS patients with a history of active disease during IFNb treatment. Patients were randomized to either cyclophosphamide 800 mg/m(2) plus methylprednisolone 1 g IV (CY/MP) or methylprednisolone once a month for six months and then followed for an additional 18 months. All patients received three days of methylprednisolone 1 g IV at screening and 30 mcg IFN beta-1a IM weekly for the entire 24 months. The primary endpoint was change from baseline in the mean number of gadolinium-enhancing (Gd+) lesions. Secondary clinical endpoints included time to treatment failure. Results: Fifty-nine patients were randomized to treatment: 30 to CY/MP and 29 to MP. Change from baseline in the number of Gd+ lesions was significantly different between treatment groups at three ( P = 0.01), six ( P = 0.04) and 12 months ( P = 0.02), with fewer lesions in the CY/MP group. The cumulative rate of treatment failure was significantly lower in the CY/MP group compared with the MP group ( rate ratio = 0.30; 95% confidence interval, 0.12 - 0.75; P = 0.011). CY/MP treatment was well tolerated. Conclusion: Combination therapy with CY/MP and IFN beta-1a decreased the number of Gd+ lesions and slowed clinical activity in patients with previously active disease on IFN beta alone.
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