RESULTS OF BONE-MARROW TRANSPLANTATION FO R HEMATOLOGIC MALIGNANCIES AND SOLID TUMORS IN INNSBRUCK

Citation
D. Nachbaur et al., RESULTS OF BONE-MARROW TRANSPLANTATION FO R HEMATOLOGIC MALIGNANCIES AND SOLID TUMORS IN INNSBRUCK, Wiener Klinische Wochenschrift, 106(7), 1994, pp. 201-207
Citations number
30
Categorie Soggetti
Medicine, General & Internal
ISSN journal
00435325
Volume
106
Issue
7
Year of publication
1994
Pages
201 - 207
Database
ISI
SICI code
0043-5325(1994)106:7<201:ROBTFR>2.0.ZU;2-1
Abstract
87 patients underwent bone marrow transplantation (BMT) in Innsbruck b etween 1983 and 1992. 81 patients were suffering from hematologic mali gnancies and severe aplastic anemia and six patients had advanced soli d tumours/sarcoma. 56% of the patients undergoing HLA-identical siblin g BMT were in an advanced or refractory stage of disease at the time o f BMT. 19 patients underwent autologous BMT and 5 patients received a graft from an HLA-matched unrelated donor. Patients were treated with standard conditioning regimens according to the underlying disease. Cy closporine A (CsA) was given prophylactically against graft-versus-hos t disease (GVHD) either alone or in combination with methotrexate. Pro bability of survival for patients transplanted in the first chronic ph ase of chronic myelogenous leukemia (CML) was 85%, whereas the disease free survival (DFS) for patients transplanted in accelerated phase or blast crisis was only 40%. DFS for acute myelogenous leukemia (AML) i n first complete remission and acute lymphoblastic leukemia (ALL) stan dard-risk (i.e., first or second complete remission) was 71% and 60%, respectively. All patients transplanted for non-Hodgkin's lymphoma (NH L) or Hodgkin's disease had refractory or advanced disease. Probabilit y of survival for lymphoma patients was 60%. Acute GVHD > grade II dev eloped in 35% of patients undergoing HLA-identical sibling BMT (46% in the high-risk group vs, 21% in the standard-risk group). Main causes of death in the high-risk group were relapse (31%), severe bacterial o r fungal infections (17%), interstitial pneumonia (11%) and acute GVHD (6%).