Results of conventional chemotherapy for multiple myeloma are disappoi
nting. High-dose chemoradiotherapy with auto-transplantation is increa
singly reported and some results are encouraging. We report the result
s of peripheral blood stem cell transplantation (PBSCT) for multiple m
yeloma at a single institution over a 6-year period. Forty patients, i
ncluding 18 de novo patients, received debulking chemotherapy consisti
ng of vincristine, adriamycin, and dexamethasone or methylprednisolone
followed by stem cell mobilization with high-dose cyclophosphamide. T
wenty-nine patients received PBSCT following high-dose chemoradiothera
py. Following PBSCT 92% of evaluable patients obtained at least a part
ial remission and 29% reached complete remission. Objective treatment
responses, defined as at least a 50% reduction in serum paraprotein or
marrow plasma cells, were observed following each treatment step of d
ebulking chemotherapy, mobilization and PBSCT in 50, 42 and 71% of pat
ients, respectively. The median overall survival from diagnosis in pat
ients transplanted was 50 months and the median overall and progressio
n-free survivals following transplant were 26 and 18 months, respectiv
ely. Median follow-up was 28 months. Overall treatment-related mortali
ty was 20% but was significantly lower in de novo vs previously treate
d patients at 6 and 33% respectively (P = 0.027). De novo patients wer
e more likely to obtain complete remission and had a longer overall su
rvival following transplant but overall survival from diagnosis was si
milar to previously treated patients. A low serum B2M before mobilizat
ion predicted a longer progression-free survival. PBSCT needs to be co
nsidered early following diagnosis to maximise treatment response and
reduce the high treatment-related mortality seen in heavily pretreated
patients. In this treatment program a dose response effect in multipl
e myeloma was observed possibly suggesting that more intensive therapy
than a single transplant may effect greater disease response.