BONE-MARROW TRANSPLANTATION FOR HEMATOLOGICAL DISEASES IN HOKKAIDO - JUNE 1985 TO DECEMBER 1991
Citation
S. Hashino et al., BONE-MARROW TRANSPLANTATION FOR HEMATOLOGICAL DISEASES IN HOKKAIDO - JUNE 1985 TO DECEMBER 1991, Japanese Journal of Clinical Oncology, 23(3), 1993, pp. 166-172
Categorie Soggetti
Oncology
SICI code
0368-2811(1993)23:3<166:BTFHDI>2.0.ZU;2-R
Abstract
Bone marrow transplantation (BMT) was started in Hokkaido in 1985. In
the present report we have reviewed the clinical outcome of patients t
reated with BMT for hematological diseases in Hokkaido. Fifty-eight al
logeneic and 19 autologous transplants were registered by December 199
1. The underlying diseases consisted of 47 leukemias, 14 lymphomas, 10
aplastic anemias and six myelodysplastic syndromes. Among the allogen
eic BMT cases, 55 were human leuhocyte antigen (HLA) identical and thr
ee were mismatched. Among the autologous BMT patiets, two recieved the
ir marrow purged with 4-hydroperoxycyclophosphamide and five, with mon
oclonal antibodies and complements. The conditioning regimens used for
malignancies were chiefly cyclophosphamide ( CY) plus total body irra
diation, or busulfan plus CY. In many cases, cytokines were used for r
apid recovery of decreased leukocytes. Engraftment was observed in 50
out of 52 evaluated allogeneic and 18 out of 19 autologous transplants
. Ten allogeneic patients suffered from severe acute graft-versus-host
diseases (GVHD), and extensive chronic GVHD appeared in 16 patients.
Relapses were observed in four cases of allogeneic BMT and six of auto
logous BMT. The major complications were interstitial pneumonitis (IP)
and severe infections. Long-term survival rates were almost 60% in bo
th allogeneic and autologous transplants. Mild acute GVHD and limited
chronic GVHD increased the survival rates. The results indicated that
substantial problems such as GVHD, IP and relapses must be controlled
in the near future for an improved outcome to be made possible.