Postrelapse survival in childhood acute lymphoblastic leukemia is independent of initial treatment intensity: a report from the Children's Oncology Group

被引:62
作者
Freyer, David R. [1 ,2 ]
Devidas, Meenakshi [3 ,4 ]
La, Mei [4 ]
Carroll, William L. [5 ]
Gaynon, Paul S. [1 ,2 ]
Hunger, Stephen P. [6 ,7 ]
Seibel, Nita L. [8 ]
机构
[1] Univ So Calif, Childrens Ctr Canc & Blood Dis, Childrens Hosp Los Angeles, Los Angeles, CA 90027 USA
[2] Univ So Calif, Keck Sch Med, Los Angeles, CA 90027 USA
[3] Univ Florida, Coll Med, Dept Epidemiol & Hlth Policy Res, Gainesville, FL USA
[4] Childrens Oncol Grp, Arcadia, CA USA
[5] NYU, Inst Canc, New York, NY USA
[6] Childrens Hosp, Dept Pediat, Aurora, CO USA
[7] Univ Colorado, Ctr Canc, Aurora, CO USA
[8] NCI, Canc Therapy Evaluat Program, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
PRIMARY THERAPY; 1ST RELAPSE; TRIALS; TRANSPLANTATION; INTENSIFICATION; CHEMOTHERAPY; MUTATION; AUSTRIA; SALVAGE; IKZF1;
D O I
10.1182/blood-2010-07-294678
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
While intensification of therapy has improved event-free survival (EFS) and survival in newly diagnosed children with acute lymphoblastic leukemia (ALL), postrelapse outcomes remain poor. It might be expected that patients relapsing after inferior initial therapy would have a higher retrieval rate than after superior therapy. In the Children's Oncology Group Study CCG-1961, significantly superior EFS and survival were achieved with an augmented (stronger) versus standard intensity regimen of postinduction intensification (PII) for children with newly diagnosed high-risk ALL and rapid day 7 marrow response (EFS/survival 81.2%/88.7% vs 71.7%/83.4%, respectively). This provided an opportunity to evaluate postrelapse survival (PRS) in 272 relapsed patients who had received randomly allocated initial treatment with augmented or standard intensity PII. As expected, PRS was worse for early versus late relapse, marrow versus extramedullary site, adolescent versus younger age and T versus B lineage. However, no difference in 3-year PRS was detected for having received augmented versus standard intensity PII (36.4% +/- 5.7% vs 39.2% +/- 4.1%; log rank P = .72). Similar findings were noted within subanalyses by timing and site of relapse, age, and immunophenotype. These findings provide insight into mechanisms of relapse in ALL, and are consistent with emergence of a resistant subclone that has acquired spontaneous mutations largely independent of initial therapy. This study is registered at www.clinicaltrials.gov as NCT00002812. (Blood. 2011; 117(11):3010-3015)
引用
收藏
页码:3010 / 3015
页数:6
相关论文
共 48 条
[1]  
[Anonymous], 2009, United States cancer statistics: 1999-2005 incidence and mortality Web-based report
[2]  
Attarbaschi A, 2002, WIEN KLIN WOCHENSCHR, V114, P148
[3]   Tumor regression in cancer patients by very low doses of a T cell-engaging antibody [J].
Bargou, Ralf ;
Leo, Eugen ;
Zugmaier, Gerhard ;
Klinger, Matthias ;
Goebeler, Mariele ;
Knop, Stefan ;
Noppeney, Richard ;
Viardot, Andreas ;
Hess, Georg ;
Schuler, Martin ;
Einsele, Hermann ;
Brandl, Christian ;
Wolf, Andreas ;
Kirchinger, Petra ;
Klappers, Petra ;
Schmidt, Margit ;
Riethmueller, Gert ;
Reinhardt, Carsten ;
Baeuerle, Patrick A. ;
Kufer, Peter .
SCIENCE, 2008, 321 (5891) :974-977
[4]   Unrelated donor stem cell transplantation compared with chemotherapy for children with acute lymphoblastic leukemia in a second remission: a matched-pair analysis [J].
Borgmann, A ;
von Stackelberg, A ;
Hartmann, R ;
Ebell, W ;
Klingebiel, T ;
Peters, C ;
Henze, G .
BLOOD, 2003, 101 (10) :3835-3839
[5]   Dexamethasone versus prednisone and daily oral versus weekly intravenous mercaptopurine for patients with standard-risk acute lymphoblastic leukemia: a report from the Children's Cancer Group [J].
Bostrom, BC ;
Sensel, MR ;
Sather, HN ;
Gaynon, PS ;
La, MK ;
Johnston, K ;
Erdmann, GR ;
Gold, S ;
Heerema, NA ;
Hutchinson, RJ ;
Provisor, AJ ;
Trigg, ME .
BLOOD, 2003, 101 (10) :3809-3817
[6]   Long-term follow-up of relapsed childhood acute lymphoblastic leukaemia [J].
Chessells, JM ;
Veys, P ;
Kempski, H ;
Henley, P ;
Leiper, A ;
Webb, D ;
Hann, IM .
BRITISH JOURNAL OF HAEMATOLOGY, 2003, 123 (03) :396-405
[7]   Long-term results of the Italian Association of Pediatric Hematology and Oncology (AIEOP) Studies 82, 87, 88, 91 and 95 for childhood acute lymphoblastic leukemia [J].
Conter, V. ;
Arico, M. ;
Basso, G. ;
Biondi, A. ;
Barisone, E. ;
Messina, C. ;
Parasole, R. ;
De Rossi, G. ;
Locatelli, F. ;
Pession, A. ;
Santoro, N. ;
Micalizzi, C. ;
Citterio, M. ;
Rizzari, C. ;
Silvestri, D. ;
Rondelli, R. ;
Lo Nigro, L. ;
Ziino, O. ;
Testi, A. M. ;
Masera, G. ;
Valsecchi, M. G. .
LEUKEMIA, 2010, 24 (02) :255-264
[8]   Cooperative study group for childhood acute lymphoblastic leukaemia (COALL): long-term results of trials 82,85,89,92 and 97 [J].
Escherich, G. ;
Horstmann, M. A. ;
Zimmermann, M. ;
Janka-Schaub, G. E. .
LEUKEMIA, 2010, 24 (02) :298-308
[9]   Long-term results of the children's cancer group studies for childhood acute lymphoblastic leukemia 1983-2002: A Children's Oncology Group Report [J].
Gaynon, P. S. ;
Angiolillo, A. L. ;
Carroll, W. L. ;
Nachman, J. B. ;
Trigg, M. E. ;
Sather, H. N. ;
Hunger, S. P. ;
Devidas, M. .
LEUKEMIA, 2010, 24 (02) :285-297
[10]   Bone marrow transplantation versus prolonged intensive chemotherapy for children with acute lymphoblastic leukemia and an initial bone marrow relapse within 12 months of the completion of primary therapy: Children's Oncology Group Study CCG - 1941 [J].
Gaynon, Paul S. ;
Harris, Richard E. ;
Altman, Arnold J. ;
Bostrom, Bruce C. ;
Breneman, John C. ;
Hawks, Ria ;
Steele, David ;
Zipf, Theodore ;
Stram, Daniel O. ;
Villaluna, Doodjuen ;
Trigg, Michael E. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (19) :3150-3156