The median survival of conventionally treated patients with multiple m
yeloma is 3 years. Modifications of conventional chemotherapy and the
administration of interferon-alpha have failed to show an improved sur
vival in most randomized trials. Therapy with dose-escalated alkylatin
g agents (i.e. melphalan 140 mg/m(2)) induced higher remission rates t
han conventional treatment. If followed by allogeneic or autologous he
matopoietic progenitor cell transplantation. the hematotoxicity of the
described dose-escalated treatment could be reduced. Results of trans
plantation trials are summarized and discussed, The transplantation of
autologous peripheral blood progenitor cells results in a faster hema
topoietic reconstitution and a decreased high-dose therapy-related mor
bidity compared to autologous bone marrow and should therefore be pref
erred. Although the randomized French myeloma trial showed a significa
nt survival advantage for patients following autologous transplantatio
n, further randomized prospective studies are required to evaluate the
role of blood progenitor cell transplantation after high-dose treatme
nt in multiple myeloma. Prognostical factors and future treatment moda
lities for myeloma are discussed.