Standard drug therapy of adult polymyositis, dermatomyositis and inclusion
body myositis includes high-dose corticosteroids and cytotoxic drugs (metho
trexate, azathioprine (AZA) and cyclophosphamide). Recent data are in favou
r of the early introduction of a cytotoxic or immunomodulating drug in addi
tion to corticosteroid therapy. In patients with corticosteroid- and cytoto
xic-resistant myositis, promising novel approaches to management include: i
v. megadose pulse methylprednisolone combined with cytotoxic drugs, combina
tion therapy with both methotrexate and AZA, cyclosporin, tacrolimus, fluda
rabine and iv. immunoglobulin (IVIG). Recent advances in the understanding
of the role of cytokines and complement, in the pathogenesis of myositis, h
ave led to preliminary therapeutic trials of three biological agents: etane
rcept, infliximab and anti-C5 monoclonal antibody.