The median survival of conventionally treated patients with multiple m
yeloma is 3 years. Modifications of conventional chemotherapy have fai
led to show an improved survival rate in most randomized trials. Thera
py regimens with dose-escalated alkylating agents (ie melphalan) have
induced higher remission rates in comparison to conventional treatment
modalities. With the support of autologous or allogeneic hematopoieti
c progenitor cells, it has been possible to reduce the hematoxicity of
these dose-escalated treatments. The transplantation of autologous pe
ripheral blood progenitor cells results in faster hematopoietic recons
titution with decreased high-dose therapy-related morbidity compared t
o autologous bone marrow. The randomized French myeloma trial and the
pair-mate analysis of the results of the 'total therapy' including dou
ble autografting of the Barlogie group with data from the South Wester
n Oncology Group (SWOG) showed a significant survival advantage for pa
tients following autologous transplantation. Although a graft-versus-m
yeloma effect was described, the benefit of high-dose treatment with a
llogeneic transplantation is less clear, mainly due to the high transp
lantation-related mortality rate. In this paper, results of transplant
ation trials are summarized. Prognostic factors and future treatment m
odalities for myeloma are discussed.