Objective-To review the clinical eVectiveness and costs of a range of disease modifying drugs in multiple sclerosis. Drugs included are azathioprine, cladribine, cyclophosphamide, intravenous immunoglobulin, methotrexate, and mitoxantrone. Methods-Electronic databases and bibliographies of related papers were searched for randomised controlled trials (RCTs) and systematic reviews, and experts and pharmaceutical companies were contacted for further information. Inclusion and quality criteria were assessed, data extraction undertaken by one reviewer and checked by a second reviewer, with discrepancies being resolved through discussion. Costs were obtained and costeVectiveness papers sought. Debate over the prescribing of -interferons in the treatment of multiple sclerosis continues, despite good evidence showing some benefit but at high cost. In England and Wales, the National Institute for Clinical Excellence (NICE) has been established to appraise the evidence on the clinical and cost eVectiveness of health technologies and provide guidance to the NHS. At the time of writing, it is considering -interferon and glatiramer in the treatment of multiple sclerosis. Excluded from the NICE appraisal are several other disease modifying drugs that may be used in the treatment of this disease. A comprehensive appraisal of disease modifying drugs for the treatment of multiple sclerosis should consider all competing alternatives.
Results-SeventeenThis study is, to the best of our knowledge, the first systematic review of a range of disease modifying drugs for multiple sclerosis. We were commissioned by the NHS Research and Development Health Technology Assessment (HTA) programme to undertake a rapid systematic review to appraise the evidence on the eVectiveness and cost of azathioprine, cladribine, cyclophosphamide, intravenous immunoglobulin, methotrexate, and mitoxantrone in reducing relapse rate and in limiting progression among people with multiple sclerosis. This paper summarises and takes forward analyses published in full by the HTA programme.