CHRONIC MYELOID-LEUKEMIA IN ACCELERATED PHASE - TREATMENT RESULTS WITH CONVENTIONAL CHEMOTHERAPY AND ALLOGENEIC BONE-MARROW TRANSPLANTATIONIN 96 PATIENTS

Citation
M. Griesshammer et al., CHRONIC MYELOID-LEUKEMIA IN ACCELERATED PHASE - TREATMENT RESULTS WITH CONVENTIONAL CHEMOTHERAPY AND ALLOGENEIC BONE-MARROW TRANSPLANTATIONIN 96 PATIENTS, European journal of haematology, 61(1), 1998, pp. 7-13
Citations number
26
Categorie Soggetti
Hematology
ISSN journal
09024441
Volume
61
Issue
1
Year of publication
1998
Pages
7 - 13
Database
ISI
SICI code
0902-4441(1998)61:1<7:CMIAP->2.0.ZU;2-Q
Abstract
The treatment results of 96 patients with Philadelphia-positive chroni c myeloid leukemia (CML) in accelerated phase (AP) were reviewed retro spectively. Treatment of AP consisted of allogeneic bone marrow transp lantation in 20 (14 related and 6 unrelated donors) or conventional ch emotherapy (CC) in 76 patients. Three main treatment strategies were f ollowed in the CC group: continuation (group A) or dose escalation (gr oup B) of chronic phase therapy or change of chronic phase therapy to hydroxyurea (group C). Median survival was 7.0 months in group A (rang e 1.8-110), in group B 8.3 months (range 0.9-40) and in group C 9.6 mo nths (range 1.5-47.6), p=0.89. Survival in CC was dependent on respons e to therapy as the achievement of a second chronic phase was signific antly associated (p<0.001) with a longer median survival (21 months), compared with stable accelerated phase disease (11 months) or treatmen t failure (5 months). Median survival in the BMT group was 16.7 months (range 5-77), the 5-yr probability of relapse was 25% and the 5-yr di sease-free survial was 36%. For patients <55 yr median survival after BMT was significantly prolonged compared with median survival after CC (n=45, 8.3 months, p=0.008). After developing criteria of AP, median survival in our analysis has been less than 1 yr. The results of conve ntional chemotherapy in the treatment of accelerated phase CML are dis appointing. If a suitable donor is available allogeneic BMT should be performed without delay in patients with AP.