Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.1.1.69 (
BMT
)
2,655
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The concise history of
BMT
development, from experimental studies to clinical practice, is presented. Bone marrow transplantation has been performed in
Poland
for more than ten years, starting with a few to almost 500 procedures up to 1999. The above was accomplished thanks to successive founding of the 14 active
BMT
centers throughout
Poland
, which presently perform from 10 to 130 BMTs per annum (mean 34). About 70% of the above number are autologous BMTs, the remaining are allogeneic BMTs from HLA compatible sibling donors and recently from compatible unrelated donors (URD). During the last few years there is an increasing trend in the number of hematopoietic stem cell transplantations derived from peripheral blood (PBSCT), not only in patients with leukaemias and malignant lymphomas, but also in patients with solid tumors. The
BMT
results achieved in
Poland
correspond to results obtained worldwide. In relation to other European countries there are less
BMT
teams (about 50%) and less
BMT
procedures (also about 50%) performed per annum (according to EBMT data calculated per 10 million inhabitants). Thanks to the financial support of the Polish Ministry of Health more and more patients are qualified for high dose chemotherapy, increasing their chances for long term disease free survival and, eventually, for cure.
...
PMID:Bone marrow and haematopoietic stem cell transplantation in Poland. 1082 89
Retrospective analysis of 102 children with CML from 9 paediatric centres in
Poland
has been performed. A total number of 102 children: 58 boys and 44 girls aged 1-17 years (median 9.4 years old) with CML, treated in the period 1975-1999 were included in the study. Forty eight of 102 (47.1 %) children were treated with cytostatic drugs without IFN alpha: busulfan, hydroxyurea, 6-mercaptopurine or etoposide (VP-16). Fifty four of 102 (52.9%) patients were treated with interferon alpha (IFN alpha) after cytoreductive pretreatment. Thirty out of 102 (29.4%) patients underwent stem cell transplantation (SCT): 24 - matched related donor allo-
BMT
, 2 - matched unrelated donor allo-
BMT
, 1 - partially matched related donor T-cell depleted allo-PBPCT, 1 - syngeneic allo-
BMT
and 2 - autologous PBPCT. Overall survival analysis revealed that 46 of the 102 (45.1%) children remained alive: 5/35 (14.3%) children treated with cytostatics alone, 22/37 (59.5%) children treated with IFN alpha and 19/30 (63.3%) children treated with SCT. Among SCT survivors there are 10/17 (58.8%) children treated with IFN alpha prior to SCT and 9/13 (69.2%) children treated with cytostatics alone prior to SCT. The probability of 5-year survival is 0.51 in the group treated with SCT (median follow-up 58 months); 0.43 in the group treated with IFN alpha (median follow-up 53 months) and 0.23 in the group treated with cytostatics (median follow-up 31 months). Our data show, that
BMT
is the treatment of choice in CML in children. IFN alpha could be successfully applied as an alternative treatment for those, who do not have a suitable donor for allogeneic SCT. Better outcome in post
BMT
children, who were not treated with IFN alpha prior to SCT requires confirmation by studies on larger groups of patients. However, it seems to be justified to stop IFN alpha therapy at least 3 months before SCT. The main reason for unsuccessful treatment outcome in patients with CML in
Poland
remains the still insufficient access to MUD-
BMT
.
...
PMID:[Results of treatment of children with chronic myelogenous leukaemia (CML) obtained by the Polish Paediatric Leukaemia/Lymphoma Study Group]. 1202 62
Sixty children with MDS treated in six centres of the Polish Paediatric Leukaemia/Lymphoma Study Group in the period 1975-1999 were included in the study. In 20 children RAEB-T, in 13 RA, in 21 RAEB and in 6 CMML were diagnosed. Our own and literature data showed that
BMT
is the best therapy for children with MDS. We need a new comprehensive protocol for the diagnosis and treatment of children with MDS in
Poland
.
...
PMID:[Results of the treatment of myelodysplastic syndrome (MDS)obtained by the Polish Paediatric Leukaemia /Lymphoma Study Group]. 1202 66