Second early allogeneic stem cell transplantations for graft failure in acute leukaemia, chronic myeloid leukaemia and aplastic anaemia
Adult
Graft Rejection
Male
Adolescent
Graft vs Host Disease
03 medical and health sciences
0302 clinical medicine
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Humans
Child
Proportional Hazards Models
Chi-Square Distribution
Leukemia
Hematopoietic Stem Cell Transplantation
Anemia, Aplastic
Infant
Middle Aged
3. Good health
Child, Preschool
Cyclosporine
Female
Immunosuppressive Agents
Follow-Up Studies
DOI:
10.1111/j.1365-2141.2000.02306.x
Publication Date:
2010-07-27T04:45:21Z
AUTHORS (15)
ABSTRACT
In this retrospective multicentre study, we analysed the results of 82 consecutive second early allogeneic transplants for primary (n = 28) or secondary (n = 54) graft failures performed between 1985 and 1997 in patients with acute leukaemia (n = 33), aplastic anaemia (n = 29) or chronic myeloid leukaemia (n = 20). HLA‐matched siblings were used in 64 cases. The same donors were used for both transplants in 56 cases and the first transplant was T‐cell depleted in 30 cases. The median age at transplant was 25 years and the median intertransplant time interval was 2 months. Estimates of the 3‐year overall survival and day 100 transplant‐related mortality were 30% and 53% respectively. A recipient age < 34 years at transplant, an intertransplant time interval ≥ 80 d and a positive recipient cytomegalovirus serology were predictors of a better outcome. The use of cyclosporin A (CsA) after second transplant had a dramatic impact on outcome, the best results being observed with CsA alone. The day 40 probability of neutrophil recovery was 73%. The use of peripheral blood progenitor cells (PBPCs) was associated with a higher and faster neutrophil recovery. Other factors associated with neutrophil recovery were an intertransplant time interval ≥ 80 d and a positive recipient cytomegalovirus serology. Therefore, second early allogeneic transplantation for graft failure is an effective treatment, especially if patients can receive CsA for graft‐versus‐host disease prevention and are retransplanted more than 80 d from first transplant.
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