Augmented post-induction therapy for children with high-risk acute lymphoblastic leukemia and a slow response to initial therapy

被引:323
作者
Nachman, JB
Sather, HN
Sensel, MG
Trigg, ME
Cherlow, JM
Lukens, JN
Wolff, L
Uckun, FM
Gaynon, PS
机构
[1] Childrens Canc Grp, Grp Operat Ctr, Arcadia, CA 91066 USA
[2] Univ Chicago, Sect Pediat Hematol Oncol, Chicago, IL 60637 USA
[3] Univ So Calif, Sch Med, Dept Prevent Med, Los Angeles, CA 90033 USA
[4] Univ Iowa Hosp & Clin, Div Pediat Bone Marrow Transplantat, Iowa City, IA 52242 USA
[5] Long Beach Mem Med Ctr, Dept Radiat Oncol, Long Beach, CA USA
[6] Vanderbilt Univ, Dept Pediat Hematol Oncol, Nashville, TN USA
[7] Oregon Hlth & Sci Univ, Dept Pediat Hematol Oncol, Portland, OR 97201 USA
[8] Doernbecher Childrens Hosp, Portland, OR 97201 USA
[9] Wayne Hughes Inst, St Paul, MN USA
[10] Childrens Canc Grp, Acute Lymphoblast Leukemia Biol Reference Lab, St Paul, MN USA
[11] Univ Wisconsin, Dept Pediat, Madison, WI 53706 USA
关键词
D O I
10.1056/NEJM199806043382304
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Children with high-risk acute lymphoblastic leukemia (ALL) who have a slow response to initial chemotherapy (more than 25 percent blasts in the bone marrow on day 7) have a poor outcome despite intensive therapy. We conducted a randomized trial in which such patients were treated with either an augmented intensive regimen of post-induction chemotherapy or a standard regimen of intensive post-induction chemotherapy. Methods Between January 1991 and June 1995, 311 children with newly diagnosed ALL who were either 1 to 9 years of age with white-cell counts of at least 50,000 per cubic millimeter or 10 years of age or older, had a slow response to initial therapy, and entered remission at the end of induction chemotherapy were randomly assigned to receive standard therapy (156 children) or augmented therapy (155). Those with lymphomatous features were excluded. Event-free survival and overall survival were assessed from the end of induction treatment. Results The outcome at five years was significantly better in the augmented-therapy group than in the standard-therapy group (Kaplan-Meier estimate of event-free survival [+/-SD]: 75.0+/-3.8 vs. 55.0+/-4.5 percent, P<0.001; overall survival: 78.4+/-3.7 vs. 66.7+/-4.2 percent, P=0.02). The difference between treatments was most pronounced among patients one to nine years of age, all of whom had white-cell counts of at least 50,000 per cubic millimeter (P<0.001). Risk factors for an adverse event in the entire cohort included a white-cell count of 200,000 per cubic millimeter or higher (P=0.004), race other than black or white (P<0.001), and the presence of a t(9;22) translocation (P=0.007). The toxic effects of augmented therapy were considerable but manageable. Conclusions Augmented post-induction chemotherapy results in an excellent outcome for most patients with high-risk ALL and a slow response to initial therapy. (C) 1998, Massachusetts Medical Society.
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页码:1663 / 1671
页数:9
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