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Treatment strategy and long-term results in paediatric patients treated in consecutive UK AML trials

Treatment strategy and long-term results in paediatric patients treated in consecutive UK AML trials
Treatment strategy and long-term results in paediatric patients treated in consecutive UK AML trials
Between 1988 and 2002, 758 children with acute myeloid leukaemia (AML) were treated on Medical Research Council (MRC) AML 10 and AML 12. MRC AML 10 tested the role of bone marrow transplantation following four blocks of intensive chemotherapy and found that while both allogeneic bone marrow transplant (allo-BMT) and autologous bone marrow transplant (A-BMT) significantly reduced the relapse risk (RR), this did not translate into a significant improvement in overall survival (OS). A risk group stratification based on cytogenetics and response to the first course of chemotherapy derived from MRC AML 10 was used to deliver risk-directed therapy in MRC AML 12. Allo-BMT was limited to standard and poor risk patients and A-BMT was not employed. Instead, the benefit of an additional block of treatment was tested by randomising children to receive either four or five blocks of treatment in total. While the results of MRC AML 12 remain immature, there appears to be no survival advantage for a fifth course of treatment. The 5 year OS, disease-free survival (DFS), event-free survival (EFS) and RR in MRC AML 12 are 66, 61, 56 and 35%, respectively; at present superior to MRC AML 10, which had a 5-year OS, DFS, EFS and RR of 58, 53, 49 and 42%, respectively. MRC AML trials employ a short course of triple intrathecal chemotherapy alone for CNS-directed treatment and CNS relapse is uncommon. Improvements in supportive care have contributed to improved outcomes and the number of deaths in remission fell between trials. Anthracycline-related cardiotoxicity remains a concern and the current MRC AML 15 trial tests the feasibility of reducing anthracycline dosage without compromising outcome by comparing standard MRC anthracycline-based consolidation with high-dose ara-C. MRC studies suggest that the role of allo-BMT is limited in 1st CR and that there may be a ceiling of benefit from current or conventional chemotherapy.
0887-6924
2130-2138
Gibson, B.E.
c31462a8-e936-4968-a4ba-bdd1a37679f8
Wheatley, K.
ff351180-4419-4585-8bcb-81baff49bfa8
Hann, I.M.
b8b85f3a-b894-45a4-b38a-4b332fe8df30
Stevens, R.F.
56316ca6-5b1c-480d-bc1b-1062342109bb
Webb, D.
711bb5db-23df-4fad-930a-a43ba5439f92
Hills, R.K.
eb673ae3-7ede-4fd6-980d-3a7dc1613345
De Graaf, S.S.
450fd5d4-aae4-4db0-9ac5-32611ff7302b
Harrison, C.J.
9c9f6b47-8bfc-49dd-b156-74539b170291
Gibson, B.E.
c31462a8-e936-4968-a4ba-bdd1a37679f8
Wheatley, K.
ff351180-4419-4585-8bcb-81baff49bfa8
Hann, I.M.
b8b85f3a-b894-45a4-b38a-4b332fe8df30
Stevens, R.F.
56316ca6-5b1c-480d-bc1b-1062342109bb
Webb, D.
711bb5db-23df-4fad-930a-a43ba5439f92
Hills, R.K.
eb673ae3-7ede-4fd6-980d-3a7dc1613345
De Graaf, S.S.
450fd5d4-aae4-4db0-9ac5-32611ff7302b
Harrison, C.J.
9c9f6b47-8bfc-49dd-b156-74539b170291

Gibson, B.E., Wheatley, K., Hann, I.M., Stevens, R.F., Webb, D., Hills, R.K., De Graaf, S.S. and Harrison, C.J. (2005) Treatment strategy and long-term results in paediatric patients treated in consecutive UK AML trials. Leukemia, 19 (12), 2130-2138. (doi:10.1038/sj.leu.2403924).

Record type: Article

Abstract

Between 1988 and 2002, 758 children with acute myeloid leukaemia (AML) were treated on Medical Research Council (MRC) AML 10 and AML 12. MRC AML 10 tested the role of bone marrow transplantation following four blocks of intensive chemotherapy and found that while both allogeneic bone marrow transplant (allo-BMT) and autologous bone marrow transplant (A-BMT) significantly reduced the relapse risk (RR), this did not translate into a significant improvement in overall survival (OS). A risk group stratification based on cytogenetics and response to the first course of chemotherapy derived from MRC AML 10 was used to deliver risk-directed therapy in MRC AML 12. Allo-BMT was limited to standard and poor risk patients and A-BMT was not employed. Instead, the benefit of an additional block of treatment was tested by randomising children to receive either four or five blocks of treatment in total. While the results of MRC AML 12 remain immature, there appears to be no survival advantage for a fifth course of treatment. The 5 year OS, disease-free survival (DFS), event-free survival (EFS) and RR in MRC AML 12 are 66, 61, 56 and 35%, respectively; at present superior to MRC AML 10, which had a 5-year OS, DFS, EFS and RR of 58, 53, 49 and 42%, respectively. MRC AML trials employ a short course of triple intrathecal chemotherapy alone for CNS-directed treatment and CNS relapse is uncommon. Improvements in supportive care have contributed to improved outcomes and the number of deaths in remission fell between trials. Anthracycline-related cardiotoxicity remains a concern and the current MRC AML 15 trial tests the feasibility of reducing anthracycline dosage without compromising outcome by comparing standard MRC anthracycline-based consolidation with high-dose ara-C. MRC studies suggest that the role of allo-BMT is limited in 1st CR and that there may be a ceiling of benefit from current or conventional chemotherapy.

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Published date: 2005
Additional Information: Orignal manuscript

Identifiers

Local EPrints ID: 26323
URI: http://eprints.soton.ac.uk/id/eprint/26323
ISSN: 0887-6924
PURE UUID: 2ed9331b-5eb2-4c7f-8eda-161b5960e638

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Date deposited: 12 Apr 2006
Last modified: 15 Mar 2024 07:09

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Contributors

Author: B.E. Gibson
Author: K. Wheatley
Author: I.M. Hann
Author: R.F. Stevens
Author: D. Webb
Author: R.K. Hills
Author: S.S. De Graaf
Author: C.J. Harrison

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