AUTOLOGOUS OR ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR ACUTE MYELOBLASTIC-LEUKEMIA IN 2ND COMPLETE REMISSION - IMPORTANCE OF DURATION OF FIRST COMPLETE REMISSION IN FINAL OUTCOME

Citation
Jf. Tomas et al., AUTOLOGOUS OR ALLOGENEIC BONE-MARROW TRANSPLANTATION FOR ACUTE MYELOBLASTIC-LEUKEMIA IN 2ND COMPLETE REMISSION - IMPORTANCE OF DURATION OF FIRST COMPLETE REMISSION IN FINAL OUTCOME, Bone marrow transplantation, 17(6), 1996, pp. 979-984
Citations number
35
Categorie Soggetti
Hematology,Oncology,Immunology,Transplantation
Journal title
ISSN journal
02683369
Volume
17
Issue
6
Year of publication
1996
Pages
979 - 984
Database
ISI
SICI code
0268-3369(1996)17:6<979:AOABTF>2.0.ZU;2-E
Abstract
Between May 1983 and March 1994, 31 patients with AML in second CR und erwent BMT. Fifteen underwent allogeneic BMT from an HLA-identical sib ling donor and 16 without a donor, unpurged ABMT. Two different prepar ative regimens were used: CY (120 mg/kg) and 12 Gy of fractioned TBI ( 19 patients), and Bu (16 mg/kg) and Cy (120 mg/kg) (BuCy2) in 12 patie nts. Main clinical characteristics including age, sex, length of first remission, FAB type, and number of leukocytes at diagnosis were simil ar in both groups. A combination of MTX and CsA was used in 13 cases w hereas either CsA or MTX alone was employed in the other two patients. With a median follow-up of 5 years the actuarial 5 year probability o f disease-free survival (DFS) for the whole group was 39.8% (95% CI: 2 9.5-50.1%). The 5 year DFS was equivalent for those who received eithe r ABMT (41.6 +/- 14.2%) or allogeneic BMT (40 +/- 15%). Probabilities of relapse and non-relapse mortality for ABMT and allo BMT patients we re 48.7 +/- 16.1 and 18.7 +/- 14.3, and 30.1 +/- 19.2 and 40.7 +/- 16. 9, respectively. DFS was better in those patients with a longer durati on of first CR (>18 months) 62.5 +/- 14.4 vs 30.4 +/- 17.9%, attributa ble to a significantly lower relapse rate in this group of patients 16 .6 +/- 12.8 vs 57.8 +/- 22.7 (P 0.05). In conclusion, similar results were observed when ABMT and allo BMT were compared for AML in CR2. A h igher antileukemic effect associated with the allo BMT is balanced by an increase in transplant-related mortality. Duration of first remissi on was the most important factor affecting DFS and better outcome was observed for patients with longer CR1.