Clinical heart failure in a cohort of children treated with anthracyclines: A long-term follow-up study

被引:209
作者
van Dalen, Elvira C.
van der Pal, Helena J. H.
Kok, Wouter E. M.
Caron, Huib N.
Kremer, Leontien C. M.
机构
[1] Univ Amsterdam, Acad Med Ctr, Emma Kinderziekenhuis, Dept Paediat Oncol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Emma Kinderziekenhuis, Late Effects Outpatient Clin, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Med Oncol, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Dept Cardiol, NL-1105 AZ Amsterdam, Netherlands
关键词
anthracyclines; paediatric cancer; congestive heart failure;
D O I
10.1016/j.ejca.2006.08.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The cumulative incidence of anthracycline-induced clinical heart failure (A-CHF) in a large cohort of 830 children treated with a mean cumulative anthracycline dose of 288 mg/m(2) (median 280 mg/m(2); range 15-900 mg/m(2)) with a very long and complete follow-up after the start of anthracycline therapy (mean 8.5 years; median 7.1 years; range 0.01-28.4 years) was 2.5%. A cumulative anthracycline dose of 300 mg/m(2) or more was the only independent risk factor (relative risk (RR) = 8). The estimated risk of A-CHF increased with time to 5.5% at 20 years after the start of anthracycline therapy; 9.8% if treated with 300 mg/m(2) or more. In conclusion, 1 in every 10 children treated with a cumulative anthracychne dose of 300 mg/m(2) or more will eventually develop A-CHR This is an extremely high risk and it reinforces the need of re-evaluating the cumulative anthracycline dose used in different treatment protocols and to define strategies to prevent A-CHF which could be implemented in treatment protocols. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3191 / 3198
页数:8
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