Intensification of therapy for children with lower-risk acute lymphoblastic leukemia: Long-term follow-up of patients treated on Children's Cancer Group trial 1881

被引:36
作者
Hutchinson, RJ
Gaynon, PS
Sather, H
Bertolone, SJ
Cooper, HA
Tannous, R
Wells, LM
Heerema, NA
Sailer, S
Trigg, ME
机构
[1] Univ Michigan Hlth Syst, Ann Arbor, MI USA
[2] Childrens Hosp, Los Angeles, CA 90027 USA
[3] Univ So Calif, Los Angeles, CA USA
[4] Univ Louisville, Louisville, KY 40292 USA
[5] Univ N Carolina, Chapel Hill, NC USA
[6] Univ Iowa Hosp & Clin, Iowa City, IA 52242 USA
[7] Richland Mem Hosp, Columbia, SC USA
[8] Ohio State Univ, Columbus, OH 43210 USA
[9] Alfred I DuPont Hosp Children, Wilmington, DE USA
关键词
D O I
10.1200/JCO.2003.03.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose : From December 1988 through December 1992, the Children's Cancer Group (CCG) conducted a randomized trial (CCG-1881) designed to evaluate the impact of adding a single delayed intensification phase of therapy to standard therapy for patients with newly diagnosed low-risk acute lymphoblastic leukemia (ALL). Patients and Methods: Patients (n = 778) with newly diagnosed ALL, 2 to 9 years of age at diagnosis with an initial WBC count less than I 0,000/muL, were eligible for this protocol. All patients received induction, consolidation, and interim maintenance phases of therapy over the first 16 weeks. At week 16, patients remaining in remission were randomly assigned to receive or not receive a single 7-week delayed intensification (DI) phase of therapy. Maintenance therapy was given in lieu of or after DI, with total duration of therapy approximately 3 years for boys and 2 years for girls. Results: Patients randomized to receive DI experienced fewer relapse events in all categories. Kaplan-Meier life-table estimates for continuous complete remission (CCR) at 7 years for the randomized regimens were 77% (SE, 2.4%) for the standard regimen and 83% (SE, 2.7%) for the DI regimen (P = .072). The only prognostic factor of significance post-randomization in this selected low-risk population was the day 14 marrow response (P = .0001). Conclusion: The addition of a single DI phase of therapy was well tolerated and augmented 7-year CCR by 6% (SE of the difference, 3.3%), resulting in 26% fewer adverse events. Overall survival for eligible patients at 7 years is 90% (SE, 1.2%). (C) 2003 by American Society of Clinical Oncology.
引用
收藏
页码:1790 / 1797
页数:8
相关论文
共 25 条
[21]   Uniform approach to risk classification and treatment assignment for children with acute lymphoblastic leukemia [J].
Smith, M ;
Arthur, D ;
Camitta, B ;
Carroll, AJ ;
Crist, W ;
Gaynon, P ;
Gelber, R ;
Heerema, N ;
Korn, EL ;
Link, M ;
Murphy, S ;
Pui, CH ;
Pullen, J ;
Reaman, G ;
Sallan, SE ;
Sather, H ;
Shuster, J ;
Simon, R ;
Trigg, M ;
Tubergen, D ;
Uckun, F ;
Ungerleider, R .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (01) :18-24
[22]  
STEINHERZ PG, 1991, CANCER-AM CANCER SOC, V68, P751, DOI 10.1002/1097-0142(19910815)68:4<751::AID-CNCR2820680416>3.0.CO
[23]  
2-T
[24]  
Stork LC, 2000, BLOOD, V96, p466A
[25]   IMPROVED OUTCOME WITH DELAYED INTENSIFICATION FOR CHILDREN WITH ACUTE LYMPHOBLASTIC-LEUKEMIA AND INTERMEDIATE PRESENTING FEATURES - A CHILDRENS-CANCER-GROUP PHASE-III TRIAL [J].
TUBERGEN, DG ;
GILCHRIST, GS ;
OBRIEN, RT ;
COCCIA, PF ;
SATHER, HN ;
WASKERWITZ, MJ ;
HAMMOND, GD .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (03) :527-537