Outcome of Pediatric Patients With Acute Myeloid Leukemia (AML) and-5/5q-Abnormalities From Five Pediatric AML Treatment Protocols: A Report From the Children's Oncology Group

被引:22
作者
Johnston, Donna L. [1 ]
Alonzo, Todd A. [2 ]
Gerbing, Robert B. [3 ]
Hirsch, Betsy [4 ]
Heerema, Nyla A. [5 ]
Ravindranath, Yaddanapudi [6 ]
Woods, William G. [7 ,8 ]
Lange, Beverly J. [9 ]
Gamis, Alan S. [10 ]
Raimondi, Susana C. [11 ]
机构
[1] Childrens Hosp Eastern Ontario, Div Hematol Oncol, Ottawa, ON K1H 8L1, Canada
[2] Univ So Calif, Dept Prevent Med, Los Angeles, CA 90089 USA
[3] Childrens Oncol Grp, Arcadia, CA USA
[4] Univ Minnesota, Med Ctr, Div Lab Med, Minneapolis, MN 55455 USA
[5] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
[6] Childrens Hosp Michigan, Div Pediat Hematol Oncol, Detroit, MI 48201 USA
[7] Emory Univ, Aflac Canc Ctr, Atlanta, GA 30322 USA
[8] Emory Univ, Childrens Healthcare Atlanta, Blood Disorders Serv, Atlanta, GA 30322 USA
[9] Childrens Hosp Philadelphia, Div Pediat Oncol, Philadelphia, PA 19104 USA
[10] Childrens Mercy Hosp & Clin, Div Hematol Oncol Bone Marrow Transplantat, Kansas City, MO USA
[11] St Jude Childrens Res Hosp, Dept Pathol, Memphis, TN 38105 USA
关键词
-5; 5q-abnormalities; acute myeloid leukemia; chromosome; 5; outcome; pediatric AML; MONOSOMAL KARYOTYPE; COMPLEX KARYOTYPE; POOR-PROGNOSIS; RISK; THERAPY; MO; TRANSPLANTATION; ABNORMALITIES; CHROMOSOME-5; CCG-2961;
D O I
10.1002/pbc.24573
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundAbnormalities of chromosome 5q (-5/5q-) are associated with poor prognosis in adults with acute myeloid leukemia (AML). However, there are no large studies on outcomes of children with -5/5q- AML. To determine the disease correlates of this group, we retrospectively analyzed cytogenetic data from five studies of childhood AML. ProcedureData from patients whose cytogenetic clones included -5/5q-, with the exception of those with acute promyelocytic leukemia or Down syndrome, were included. ResultsOf the 2,240 patients with cytogenetic data available, 26 (1.2%) had -5 or 5q-. A significant number of these patients were age 11-21 (61.5%, P=0.031) and had M0 morphology compared with patients without -5/5q- (24.0% vs. 2.8%, P<0.001). Twenty-two of the 26 patients had a complete remission (CR) response to induction chemotherapy. The 5-year overall survival (OS) from the time of diagnosis for the -5/5q- patients was significantly lower than for patients without -5/5q- (2717% vs. 50 +/- 2%, P=0.027). Similarly, from induction CR, patients with -5/5q- had significantly worse disease free survival, OS and relapse risk than those without this abnormality (27 +/- 19% vs. 46 +/- 2%, P=0.035, 32 +/- 20% vs. 57 +/- 2%, P=0.025, 68 +/- 21% vs. 45 +/- 2%, P=0.01, respectively). ConclusionsPediatric patients with AML and -5/5q- had a very poor outcome. These findings support the need for new or novel therapies for these patients. Pediatr Blood Cancer 2013;60:2073-2078. (c) 2013 Wiley Periodicals, Inc.
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收藏
页码:2073 / 2078
页数:6
相关论文
共 26 条
[1]   Minimally differentiated acute myeloid leukemia (AML-MO): A distinct clinico-biologic entity with poor prognosis [J].
Amadori, S ;
Venditti, A ;
DelPoeta, G ;
Stasi, R ;
Buccisano, F ;
Bruno, A ;
Tamburini, A ;
Cox, MC ;
Maffei, L ;
Aronica, G ;
Simone, MD ;
Adorno, G ;
Masi, M ;
Tribalto, M ;
Papa, G .
ANNALS OF HEMATOLOGY, 1996, 72 (04) :208-215
[2]  
[Anonymous], 2011, The statistical analysis of failure time data
[3]   Minimally differentiated acute myeloid leukemia (EAB AML-M0) is associated with an adverse outcome in children: a report from the Children's Oncology Group, studies CCG-2891 and CCG-2961 [J].
Barbaric, Draga ;
Alonzo, Todd A. ;
Gerbing, Robert B. ;
Meshinchi, Soheil ;
Heerema, Nyla A. ;
Barnard, Dorothy R. ;
Lange, Beverly J. ;
Woods, William G. ;
Arceci, Robert J. ;
Smith, Franklin O. .
BLOOD, 2007, 109 (06) :2314-2321
[4]   Randomized use of cyclosporin A (CsA) to modulate P-glycoprotein in children with AML in remission: Pediatric Oncology Group Study 9421 [J].
Becton, D ;
Dahl, GV ;
Ravindranath, Y ;
Chang, MN ;
Behm, FG ;
Raimondi, SC ;
Head, DR ;
Stine, KC ;
Lacayo, NJ ;
Sikic, BI ;
Arceci, RJ ;
Weinstein, H .
BLOOD, 2006, 107 (04) :1315-1324
[5]   Acute myeloid leukaemia MO:: haematological, immunophenotypic and cytogenetic characteristics and their prognostic significance:: an analysis in 241 patients [J].
Béné, MC ;
Bernier, M ;
Casasnovas, RO ;
Castoldi, G ;
Doekharan, D ;
van der Holt, B ;
Knapp, W ;
Lemez, P ;
Ludwig, WD ;
Matutes, E ;
Orfao, A ;
Schoch, C ;
Sperling, C ;
van't Veer, MB .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (03) :737-745
[6]   Monosomal karyotype in acute myeloid leukemia:: A better indicator of poor prognosis than a complex karyotype [J].
Breems, Dimitri A. ;
Van Putten, Wim L. J. ;
De Greef, Georgine E. ;
Van Zelderen-Bhola, Shama L. ;
Gerssen-Schoorl, Klasien B. J. ;
Mellink, Clemens H. M. ;
Nieuwint, Aggie ;
Jotterand, Martine ;
Hagemeijer, Anne ;
Beverloo, H. Berna ;
Lowenberg, Bob .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (29) :4791-4797
[7]   A Phase II Study of Lenalidomide Alone in Relapsed/Refractory Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndromes With Chromosome 5 Abnormalities [J].
Chen, Yiming ;
Kantarjian, Hagop ;
Estrov, Zeev ;
Faderl, Stefan ;
Ravandi, Farhad ;
Rey, Kristy ;
Cortes, Jorge ;
Borthakur, Gautam .
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2012, 12 (05) :341-344
[8]   AAML03P1, a pilot study of the safety of gemtuzumab ozogamicin in combination with chemotherapy for newly diagnosed childhood acute myeloid leukemia [J].
Cooper, Todd M. ;
Franklin, Janet ;
Gerbing, Robert B. ;
Alonzo, Todd A. ;
Hurwitz, Craig ;
Raimondi, Susana C. ;
Hirsch, Betsy ;
Smith, Franklin O. ;
Mathew, Prasad ;
Arceci, Robert J. ;
Feusner, James ;
Iannone, Robert ;
Lavey, Robert S. ;
Meshinchi, Soheil ;
Gamis, Alan .
CANCER, 2012, 118 (03) :761-769
[9]  
CREUTZIG U, 1995, BLOOD, V86, P3097
[10]   CYTOGENETIC PROFILE OF MINIMALLY DIFFERENTIATED (FAB M0) ACUTE MYELOID-LEUKEMIA - CORRELATION WITH CLINICOBIOLOGIC FINDINGS [J].
CUNEO, A ;
FERRANT, A ;
MICHAUX, JL ;
BOOGAERTS, M ;
DEMUYNCK, H ;
VANORSHOVEN, A ;
CRIEL, A ;
STUL, M ;
DALCIN, P ;
HERNANDEZ, J ;
CHATELAIN, B ;
DOYEN, C ;
LOUWAGIE, A ;
CASTOLDI, G ;
CASSIMAN, JJ ;
VANDENBERGHE, H .
BLOOD, 1995, 85 (12) :3688-3694