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Vol 279 No 7465 p174
18 August 2007

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Interferon beneficial for patients with suspected MS

Scott Camazine/Science Photo Library

Multiple sclerosis

MS less likely to develop at three years if patients are treated early with interferon

Patients given interferon after a neurological episode suggestive of multiple sclerosis (MS) are less likely to develop clinically definite MS than those given placebo, a three-year follow-up study has shown (Lancet 2007;370:389).

Researchers initially randomised patients with a first event suggestive of MS and at least two “clinically silent lesions” to receive either interferon beta-1b or placebo every other day for two years, after which patients were offered open-label interferon treatment. Three years after the initial randomisation, patients given early interferon were compared with those who started treatment after two years or after MS diagnosis.

The researchers found that 34 per cent of patients in the early treatment group developed clinically definite MS compared with 48 per cent in the delayed group (absolute risk reduction 14 per cent; P=0.0011). Patients given interferon early were also at a reduced risk of confirmed “expanded disability status scale” (EDSS) progression than those in the delayed treatment group (absolute risk reduction 8 per cent; P=0.022). The researchers calculated that 12 patients would need to be treated early to avoid a single confirmed EDSS progression.

Nevertheless, in an accompanying editorial (ibid, p363), Sean Pittock, of the Mayo Clinic College of Medicine, Rochester, Minnesota, says that controversy still exists about who and when to treat. He highlights a lack of significant benefit of early treatment over delaying it for patients with limited clinical signs or symptoms (over half of participants) or limited disease dissemination by radiographic measurement (over a quarter of subjects).

Dr Pittock says: “[The authors] present the first evidence that interferon beta-1b treatment has a beneficial effect on accumulation of confirmed disability in patients with a first event suggestive of multiple sclerosis. The results should, however, be interpreted with care because the magnitude of benefit, although statistically significant, is clinically small.” He suggests that the results should not be misconstrued as evidence for a treat-all approach.

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