Analysis of the Role of Hematopoietic Stem-Cell Transplantation in Infants With Acute Lymphoblastic Leukemia in First Remission and MLL Gene Rearrangements: A Report From the Children's Oncology Group

被引:60
作者
Dreyer, Zoann E.
Dinndorf, Patricia A.
Camitta, Bruce
Sather, Harland
La, Mei K.
Devidas, Meenakshi
Hilden, Joanne M.
Heerema, Nyla A.
Sanders, Jean E.
McGlennen, Ron
Willman, Cheryl L.
Carroll, Andrew J.
Behm, Fred
Smith, Franklin O.
Woods, William G.
Godder, Kamar
Reaman, Gregory H.
机构
[1] Texas Childrens Hosp, Houston, TX 77030 USA
[2] US FDA, Silver Spring, MD USA
[3] Midwest Childrens Canc Ctr, Milwaukee, WI USA
[4] Childrens Oncol Grp, Arcadia, CA USA
[5] Peyton Manning Childrens Hosp St Vincent, Indianapolis, IN USA
[6] Nationwide Childrens Hosp, Columbus, OH USA
[7] Seattle Childrens Hosp, Seattle, WA USA
[8] Univ Minnesota Med Sch, Minneapolis, MN USA
[9] Univ New Mexico Sch Med, Albuquerque, NM USA
[10] Univ Alabama, Birmingham, AL USA
[11] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH USA
[12] Univ Illinois, Chicago, IL USA
[13] Emory Univ Childrens Healthcare Atlanta, Aflac Canc Ctr, Atlanta, GA USA
[14] Virginia Commonwealth Univ Hlth Care Syst, Med Coll Virginia, Richmond, VA USA
基金
美国国家卫生研究院;
关键词
BONE-MARROW-TRANSPLANTATION; PROGNOSTIC-FACTORS; CLINICAL-TRIALS; POOR-PROGNOSIS; CANCER GROUP; CHILDHOOD; IRRADIATION;
D O I
10.1200/JCO.2009.26.8938
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Although the majority of children with acute lymphoblastic leukemia (ALL) are cured with current therapy, the event-free survival (EFS) of infants with ALL, particularly those with mixed lineage leukemia (MLL) gene rearrangements, is only 30% to 40%. Relapse has been the major source of treatment failure for these patients. The parallel Children's Cancer Group (CCG) 1953 and Pediatric Oncology Group (POG) 9407 studies were designed to test the hypothesis that more intensive therapy, including dose intensification of chemotherapy, and hematopoietic stem-cell transplantation (HSCT) would improve the outcome for this group of patients. Patients and Methods One hundred eighty-nine infants (CCG 1953, n = 115; POG 9407, n = 74) were enrolled between October 1996 and August 2000. For infants with the MLL gene rearrangement and an appropriate donor, HSCT was the preferred treatment on CCG 1953 and investigator option on POG 9407 after completion of the second phase of therapy. Fifty-three infants underwent HSCT. Results The 5-year EFS rate was 48.8% (95% CI, 33.9% to 63.7%) in patients who received HSCT and 48.7% (95% CI, 33.8% to 63.6%) in patients treated with chemotherapy alone (P = .60). Transplantation outcomes were not affected by the preparatory regimen or donor source. Conclusion Our data suggest that routine use of HSCT for infants with MLL-rearranged ALL is not indicated. However, limited by small numbers, this study should not be considered the definitive answer to this question. J Clin Oncol 29:214-222. (C) 2010 by American Society of Clinical Oncology
引用
收藏
页码:214 / 222
页数:9
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