The role of matched sibling donor allogeneic stem cell transplantation in pediatric high-risk acute myeloid leukemia: results from the AML-BFM 98 study

被引:60
作者
Klusmann, Jan-Henning [2 ]
Reinhardt, Dirk [2 ]
Zimmermann, Martin [2 ]
Kremens, Bernhard [3 ]
Vormoor, Josef [4 ,5 ,6 ,7 ]
Dworzak, Michael [8 ,9 ]
Creutzig, Ursula [1 ]
Klingebiel, Thomas [10 ]
机构
[1] Univ Childrens Hosp, Dept Pediat Hematol & Oncol, D-48149 Munster, Germany
[2] Hannover Med Sch, Dept Pediat Hematol Oncol, D-3000 Hannover, Germany
[3] Univ Childrens Hosp, Dept Pediat Hematol & Oncol, Essen, Germany
[4] No Inst Canc Res, Newcastle Upon Tyne, Tyne & Wear, England
[5] Newcastle Univ, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[6] Sir James Spence Inst, Newcastle Upon Tyne, Tyne & Wear, England
[7] Royal Victoria Infirm, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[8] St Anna Childrens Hosp, Vienna, Austria
[9] St Anna Childrens Hosp, Childrens Canc Res Inst, A-1090 Vienna, Austria
[10] Univ Childrens Hosp III, Frankfurt, Germany
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2012年 / 97卷 / 01期
关键词
acute myeloid leukemia; AML; stem cell transplantation; SCT; MLL childhood; post-remission therapy; BONE-MARROW-TRANSPLANTATION; HEMATOLOGY-AND-IMMUNOLOGY; BRITISH COOPERATIVE GROUP; CHILDRENS-ONCOLOGY-GROUP; FRENCH-SOCIETY; INTENSIVE CHEMOTHERAPY; CANCER GROUP; TRIAL; THERAPY; REMISSION;
D O I
10.3324/haematol.2011.051714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The role of allogeneic stem cell transplantation in post-remission management of children with high-risk acute myeloid leukemia remains controversial. In the multi-center AML-BFM 98 study we prospectively evaluated the impact of allogeneic stem cell transplantation in children with high-risk acute myeloid leukemia in first complete remission. Design and Methods HLA-typed patients with high-risk acute myeloid leukemia, who achieved first complete remission (n = 247), were included in this analysis. All patients received double induction and consolidation. Based on the availability of a matched-sibling donor, patients were allocated by genetic chance to allogeneic stem cell transplantation (n = 61) or chemotherapy-only (i.e. intensification and maintenance therapy; n = 186). The main analysis was done on an intention-to-treat basis according to this allocation. Results Intention-to-treat analysis did not show a significantly different 5-year disease-free survival (49 +/- 6% versus 45 +/- 4%, P-log rank = 0.44) or overall survival (68 +/- 6% versus 57 +/- 4%, P-log rank = 0.17) between the matched-sibling donor and no-matched-sibling donor groups, whereas late adverse effects occurred more frequently after allogeneic stem cell transplantation (72.5% versus 31.8%, P-Fischer<0.01). These results were confirmed by as-treated analysis corrected for the time until transplantation (5-year overall survival: 72 +/- 8% versus 60 +/- 4%, PMantel-Byar 0.21). Subgroup analysis demonstrated improved survival rates for patients with 11q23 aberrations allocated to allogeneic stem cell transplantation (5-year overall survival: 94 +/- 6% versus 52 +/- 7%, Plog-rank = 0.01; n = 18 versus 49) in contrast to patients without 11q23 aberrations (5-year overall survival: 58 +/- 8% versus 55 +/- 5%, Plog-rank = 0.66). Conclusions Our analyses defined a genetic subgroup of children with high-risk acute myeloid leukemia who benefited from allogeneic stem cell transplantation in the prospective multi-center AML-BFM 98 study. For the remainder of the pediatric high-risk acute myeloid leukemia patients the prognosis was not improved by allogeneic stem cell transplantation, which was, however, associated with a higher rate of late sequelae. (ClinicalTrials.gov Identifier: #NCT00111345)
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页码:21 / 29
页数:9
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