Outcome of treatment in childhood acute lymphoblastic leukaemia with rearrangements of the 11q23 chromosomal region

被引:278
|
作者
Pui, CH
Gaynon, PS
Boyett, JM
Chessells, JM
Baruchel, A
Kamps, W
Silverman, LB
Biondi, A
Harms, DO
Vilmer, E
Schrappe, M
Camitta, B
机构
[1] St Jude Childrens Res Hosp, Memphis, TN 38105 USA
[2] Univ Tennessee, Coll Med, Memphis, TN 38163 USA
[3] Childrens Hosp Los Angeles, Los Angeles, CA 90027 USA
[4] Univ So Calif, Los Angeles, CA USA
[5] Inst Child Hlth, Mol Haematol Unit, London, England
[6] Hop St Louis, Serv Pediat Hematol, Paris, France
[7] Dutch Childhood Leukemia Study Grp, The Hague, Netherlands
[8] Dana Farber Canc Inst, Boston, MA 02115 USA
[9] Harvard Med Sch, Boston, MA USA
[10] Univ Milano Bicocca, Dept Pediat, Monza, Italy
[11] Osped San Gerardo, Monza, Italy
[12] Univ Hamburg, Dept Pediat Hematol & Oncol, Hamburg, Germany
[13] Hop Robert Debre, Serv Hematoimmunol, F-75019 Paris, France
[14] Hannover Med Sch, Dept Pediat Hematol Oncol, Childrens Univ Hosp, Hannover, Germany
[15] Med Coll Wisconsin, Dept Pediat, Midwest Childrens Canc Ctr, Milwaukee, WI 53226 USA
来源
LANCET | 2002年 / 359卷 / 9321期
关键词
D O I
10.1016/S0140-6736(02)08782-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The prognosis and optimum treatment of childhood acute lymphoblastic leukaemia (ALL) with abnormalities of chromosomal band 11q23 are controversial. We aimed to identify prognostic factors that might help in planning future therapy, and to assess the effectiveness of haemopoietic stem-cell transplantation in patients with the t(4;11) translocation, which is associated with a particularly poor outcome. Methods We reviewed data on 497 children and young adults who had ALL with various 11q23 abnormalities, including the translocations t(4;11), t(9;11), and t(11;19). All patients were treated with intensive chemotherapy, with or without haemopoietic stem-cell transplantation in first complete remission, by 11 study groups and single institutions from 1983 to 1995. Findings Age was the most important prognostic factor. In a Cox's proportional-hazard model stratified by 11q23 abnormalities, infants younger than 1 year fared significantly worse than patients 1 year of age or older (hazard ratio for event-free survival 1.84 [95% CI 1.38-2.47], p=0.0001). Among infants, any category of 11q23 abnormality conferred a dismal outcome, whereas in older patients, t(4;11) and t(9;11) were associated with a worse outcome than were other 11q23 changes. In the largest subgroup-256 patients with t(4;11)-any type of transplantation was associated with significantly worse disease-free survival (1.61 [1.10-2.35], p=0.014) and overall survival (1.76 [1.08-2.45], p=0.004) compared with chemotherapy only. Even transplantation with stem cells from HLA-matched related or HLA-matched unrelated donors tended to be associated with a worse outcome than chemotherapy alone. Interpretation The prognosis of acute lymphoblastic leukaemia with an 11q23 abnormality is particularly dismal in infants. Allogeneic transplantation with haemopoietic stem cells from an HLA-matched related donor does not seem to improve the clinical outcome in patients with t(4:11)-positive leukaemia.
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页码:1909 / 1915
页数:7
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