Decreased Relapsed Rate and Treatment-Related Mortality Contribute to Improved Outcomes for Pediatric Acute Myeloid Leukemia in Successive Clinical Trials

被引:35
作者
Alexander, Thomas B. [1 ,2 ]
Wang, Lei [3 ]
Inaba, Hiroto [2 ,4 ]
Triplett, Brandon M. [5 ]
Pounds, Stanley [3 ]
Ribeiro, Raul C. [2 ,4 ]
Pui, Ching-Hon [2 ,4 ]
Rubnitz, Jeffrey E. [2 ,4 ]
机构
[1] Univ N Carolina, Dept Pediat, 170 Manning Dr,1185 Phys Off Bldg,CB 7236, Chapel Hill, NC 27599 USA
[2] St Jude Childrens Res Hosp, Dept Oncol, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Biostat, 332 N Lauderdale St, Memphis, TN 38105 USA
[4] Univ Tennessee, Ctr Hlth Sci, Coll Med, Dept Pediat, Memphis, TN 38163 USA
[5] St Jude Childrens Res Hosp, Dept Bone Marrow Transplantat & Cellular Therapy, 332 N Lauderdale St, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
leukemia; pediatric; supportive care; outcomes; MINIMAL RESIDUAL DISEASE; NONPARAMETRIC-ESTIMATION; CELL TRANSPLANTATION; SURVIVAL; AML; CYTARABINE; CHILDREN; THERAPY; DEATHS; DONOR;
D O I
10.1002/cncr.30791
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Outcomes for children with acute myeloid leukemia (AML) have improved over the past 20 years even though the medications used for induction therapy have not changed. METHODS: This study analyzed data from patients with AML who were enrolled in successive protocols (AML97 and AML02) to determine the contributors to the improved outcomes of the latter clinical trial. RESULTS: There were significant improvements in 5-year overall survival (48.9% vs 71.2%; P < .0001) and event-free survival (43.5% vs 61.8%; P = .002) from AML97 to AML02. The 5-year cumulative incidence of early death (ED)/treatment-related mortality (TRM) was reduced for patients treated in AML02 (18.5% vs 7.9%; P = .007). Although the overall incidence of refractory disease (6.5% vs 5.6%; P = .736) and relapse (29.3% vs 21.0%; P = .12) did not differ between the 2 studies, patients with low-risk AML who were treated in AML02 had a reduced incidence of relapse (27.3% vs 8.8%; P = .036). CONCLUSIONS: The improved outcomes of the AML02 trial resulted from improved disease control for low-risk patients and overall decreased ED/TRM. These results emphasize the importance of supportive-care measures throughout chemotherapy courses and hematopoietic cell transplantation and the value of treatment intensity for patients with low-risk AML while underscoring the need for novel therapy, rather than increased therapy intensity, for children with high-risk AML. (C) 2017 American Cancer Society
引用
收藏
页码:3791 / 3798
页数:8
相关论文
共 23 条
[1]   NONPARAMETRIC ESTIMATION OF PARTIAL TRANSITION-PROBABILITIES IN MULTIPLE DECREMENT MODELS [J].
AALEN, O .
ANNALS OF STATISTICS, 1978, 6 (03) :534-545
[2]   Early deaths and treatment-related mortality in children undergoing therapy for acute myeloid leukemia: Analysis of the multicenter clinical trials AML-BFM 93 and AML-BFM 98 [J].
Creutzig, U ;
Zimmermann, M ;
Reinhardt, D ;
Dworzak, M ;
Stary, J ;
Lehrnbecher, T .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (21) :4384-4393
[3]   Second induction with high-dose cytarabine and mitoxantrone: different impact on pediatric AML patients with t(8;21) and with inv(16) [J].
Creutzig, Ursula ;
Zimmermann, Martin ;
Bourquin, Jean-Pierre ;
Dworzak, Michael N. ;
von Neuhoff, Christine ;
Sander, Annette ;
Schrauder, Andre ;
Teigler-Schlegel, Andrea ;
Stary, Jan ;
Corbacioglu, Selim ;
Reinhardt, Dirk .
BLOOD, 2011, 118 (20) :5409-5415
[4]   A CLASS OF K-SAMPLE TESTS FOR COMPARING THE CUMULATIVE INCIDENCE OF A COMPETING RISK [J].
GRAY, RJ .
ANNALS OF STATISTICS, 1988, 16 (03) :1141-1154
[5]   Cytogenetics of Childhood Acute Myeloid Leukemia: United Kingdom Medical Research Council Treatment Trials AML 10 and 12 [J].
Harrison, Christine J. ;
Hills, Robert K. ;
Moorman, Anthony V. ;
Grimwade, David J. ;
Hann, Ian ;
Webb, David K. H. ;
Wheatley, Keith ;
de Graaf, Siebold S. N. ;
van den Berg, Eva ;
Burnett, Alan K. ;
Gibson, Brenda E. S. .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (16) :2674-2681
[6]   Feasibility, Efficacy, and Adverse Effects of Outpatient Antibacterial Prophylaxis in Children With Acute Myeloid Leukemia [J].
Inaba, Hiroto ;
Gaur, Aditya H. ;
Cao, Xueyuan ;
Flynn, Patricia M. ;
Pounds, Stanley B. ;
Avutu, Viswatej ;
Marszal, Lindsay N. ;
Howard, Scott C. ;
Pui, Ching-Hon ;
Ribeiro, Raul C. ;
Hayden, Randall T. ;
Rubnitz, Jeffrey E. .
CANCER, 2014, 120 (13) :1985-1992
[7]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[8]   Comparable Survival for Pediatric Acute Myeloid Leukemia With Poor-Risk Cytogenetics Following Chemotherapy, Matched Related Donor, or Unrelated Donor Transplantation [J].
Kelly, Michael J. ;
Horan, John T. ;
Alonzo, Todd A. ;
Eapen, Mary ;
Gerbing, Robert B. ;
He, Wensheng ;
Lange, Beverly J. ;
Parsons, Susan K. ;
Woods, William G. .
PEDIATRIC BLOOD & CANCER, 2014, 61 (02) :269-275
[9]   Clinical Impact of Additional Cytogenetic Aberrations, cKIT and RAS Mutations, and Treatment Elements in Pediatric t(8;21)-AML: Results From an International Retrospective Study by the International Berlin-Frankfurt-Munster Study Group [J].
Klein, Kim ;
Kaspers, Gertjan ;
Harrison, Christine J. ;
Beverloo, H. Berna ;
Reedijk, Ardine ;
Bongers, Mathilda ;
Cloos, Jacqueline ;
Pession, Andrea ;
Reinhardt, Dirk ;
Zimmerman, Martin ;
Creutzig, Ursula ;
Dworzak, Michael ;
Alonzo, Todd ;
Johnston, Donna ;
Hirsch, Betsy ;
Zapotocky, Michal ;
De Moerloose, Barbara ;
Fynn, Alcira ;
Lee, Vincent ;
Taga, Takashi ;
Tawa, Akio ;
Auvrignon, Anne ;
Zeller, Bernward ;
Forestier, Erik ;
Salgado, Carmen ;
Balwierz, Walentyna ;
Popa, Alexander ;
Rubnitz, Jeffrey ;
Raimondi, Susana ;
Gibson, Brenda .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (36) :4247-4258
[10]   Place of HSCT in treatment of childhood AML [J].
Klingebiel, T. ;
Reinhardt, D. ;
Bader, P. .
BONE MARROW TRANSPLANTATION, 2008, 42 (Suppl 2) :S7-S9