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Marrow Transplantation for Acute Lymphoblastic Leukemia: Factors Affecting Relapse and Survival
Transplant outcome was analyzed in 690 recipients of bone marrow transplants (BMTs) for acute lymphoblastic leukemia (ALL) in first (n = 299) or second remission (n = 391). Actuarial 5-year leukemia-free survival was 42% ± 9% (95% confidence interval) and 26% ± 6%, respectively; relapse rates were 2...
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Published in: | Blood 1989-08, Vol.74 (2), p.862-871 |
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Main Authors: | , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Transplant outcome was analyzed in 690 recipients of bone marrow transplants (BMTs) for acute lymphoblastic leukemia (ALL) in first (n = 299) or second remission (n = 391). Actuarial 5-year leukemia-free survival was 42% ± 9% (95% confidence interval) and 26% ± 6%, respectively; relapse rates were 29% ± 9% and 52% ± 8%, respectively. Five-year leukemia-free survival was 56% ± 18% in children and 39% ± 10% in adults (P ≪ .02) transplanted in first remission. In first-remission adults, non-T-cell phenotype, male to female donor-recipient sex-match and grafts-host disease (GVHD) were associated with decreased leukemia-free survival; inclusion of corticosteroids in the regimen to prevent GVHD was associated wth increased leukemia-free survival. Variables associated with decreased leukemia-free survival after second-remission transplants were age ≫16 years and relapse occurring while on therapy. Variables associated with increased probability of relapse were similar for first- and secondremission transplants and included GVHD prophylaxis without methotrexate and absence of GVHD. In firstremission transplants, leukocyte count ≫50 x 109/L at diagnosis was also associated with increased relapse; in second remission, relapse while receiving chemotherapy was also associated with increased posttransplant relapse. These data emphasize the importance of both disease- and transplant-related variables in predicting outcome after BMT. They may be used to explain differences between studies, design future trials, and identify persons most likely to benefit from BMT. © 1989 by Grune & Stratton, Inc. |
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ISSN: | 0006-4971 1528-0020 |
DOI: | 10.1182/blood.V74.2.862.862 |