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Treatment strategy and results in children treated on three Dutch Childhood Oncology Group acute myeloid leukemia trials
被引:40
|作者:
Kardos, G
Zwaan, CM
Kaspers, GJL
de-Graaf, SSN
de Bont, ESJM
Postma, A
Bökkerink, JPM
Weening, RS
van der Does-van den Berg, A
van Wering, ER
Korbijn, C
Hählen, K
机构:
[1] Sophia Childrens Univ Hosp, Erasmus Med Ctr, Dept Pediat Hematol Oncol, NL-3000 CB Rotterdam, Netherlands
[2] Dutch Childhood Oncol Grp, The Hague, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Dept Pediat Hematol Oncol, Amsterdam, Netherlands
[4] Univ St Radboud, Med Ctr, Dept Pediat Hematol Oncol, Nijmegen, Netherlands
[5] Univ Groningen, Med Ctr, Beatrix Children Hosp, Dept Pediat Hematol Oncol, Groningen, Netherlands
[6] Emma Childrens Hosp, Acad Med Ctr, Dept Pediat Hematol Oncol, Amsterdam, Netherlands
来源:
关键词:
Dutch Childhood Oncology Group;
acute myeloid leukemia;
follow-up;
prognosis;
D O I:
10.1038/sj.leu.2403873
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
This report describes the long-term follow-up data of three consecutive Dutch Childhood Oncology Group acute myeloid leukemia (AML) protocols. A total of 303 children were diagnosed with AML, of whom 209 were eligible for this report. The first study was the AML-82 protocol. Results were inferior (5-year probability of overall survival (pOS) 31%) to other available regimes. Study AML-87 was based on the BFM-87 protocol, with prophylactic cranial irradiation in high-risk patients only, and without maintenance therapy. This led to a higher cumulative incidence of relapse than that reported by the Berlin-Frankfurt-Munster (BFM), but survival was similar (5-year pOS 47%), suggesting successful retrieval at relapse. The subsequent study AML-92/94 consisted of a modified BFM-93 protocol, that is, without maintenance therapy and prophylactic cranial irradiation. However, all patients were to be transplanted (auto- or allogeneic), although compliance was poor. Antileukemic efficacy was offset by an increase in the cumulative incidence of nonrelapse mortality, especially in remission patients, and survival did not improve (5-year pOS 44%). Our results demonstrate that outcome in childhood AML is still unsatisfactory, and that further intensification of therapy carries the risk of enhanced toxicity. Our patients are currently included in the MRC AML studies, based on the results of their AML 10 trial.
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页码:2063 / 2071
页数:9
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