A review on allogeneic stem cell transplantation for newly diagnosed pediatric acute myeloid leukemia

被引:86
作者
Niewerth, Denise [1 ]
Creutzig, Ursula [2 ]
Bierings, Marc B. [3 ]
Kaspers, Gertjan J. L. [1 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Pediat Oncol Hematol, NL-1081 HV Amsterdam, Netherlands
[2] Univ Munster, Dept Pediat Hematol Oncol, Munster, Germany
[3] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Utrecht, Netherlands
关键词
BONE-MARROW-TRANSPLANTATION; ACUTE MYELOBLASTIC-LEUKEMIA; 1ST COMPLETE REMISSION; CHILDRENS-CANCER-GROUP; ONCOLOGY-GROUP; CONSOLIDATION CHEMOTHERAPY; CURRENT CONTROVERSIES; TREATMENT STRATEGY; AML; CHILDHOOD;
D O I
10.1182/blood-2010-01-261800
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Survival of pediatric acute myeloid leukemia (AML) has improved considerably over the past decades. Since 1985, allogeneic stem cell transplantation (allo-SCT) is widely recommended for patients who have a matched sibling donor. However, it remains controversial whether allo-SCT is superior to chemotherapy for children with newly diagnosed AML. This review summarizes phase 3 clinical trials that compared allo-SCT with chemotherapy (including autologous SCT) in pediatric AML, excluding studies that did not use the intention-to-treat analysis or correct for time-to-transplantation. Although allo-SCT might prevent more relapses than chemotherapy, the number needed for transplantation (with allo-SCT) to prevent one relapse is in the order of 10 patients. Moreover, overall survival is similar with both methods in most recent studies, apparently because of increased salvagability of a relapse when initial therapy concerned chemotherapy only, and because of a higher treatment-related mortality with allo-SCT. Because allo-SCT also gives more severe side effects and results more often in secondary malignancies than chemotherapy, we do not recommend allo-SCT in first remission for pediatric AML in general. Further research should focus on the possibility that subgroups might benefit from allo-SCT, aiming at further improvements in the prognosis of pediatric AML. (Blood. 2010;116(13):2205-2214)
引用
收藏
页码:2205 / 2214
页数:10
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