van Dalen Elvira C, van der Pal Helena J H, Kok Wouter E M, Caron Huib N, Kremer Leontien C M
Department of Pediatric Oncology, Emma Children's Hospital/Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.
Eur J Cancer. 2006 Dec;42(18):3191-8. doi: 10.1016/j.ejca.2006.08.005. Epub 2006 Sep 20.
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/m2 (median 280 mg/m2; range 15-900 mg/m2) 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/m2 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/m2 or more. In conclusion, 1 in every 10 children treated with a cumulative anthracycline dose of 300 mg/m2 or more will eventually develop A-CHF. 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.
在一个由830名儿童组成的大型队列中,蒽环类药物诱导的临床心力衰竭(A-CHF)的累积发病率为2.5%。这些儿童接受的蒽环类药物平均累积剂量为288 mg/m²(中位数280 mg/m²;范围15 - 900 mg/m²),蒽环类药物治疗开始后有非常长且完整的随访期(平均8.5年;中位数7.1年;范围0.01 - 28.4年)。300 mg/m²或更高的蒽环类药物累积剂量是唯一的独立危险因素(相对风险(RR)=8)。蒽环类药物治疗开始后20年,A-CHF的估计风险增加至5.5%;如果接受300 mg/m²或更高剂量的治疗,风险为9.8%。总之,每10名接受300 mg/m²或更高蒽环类药物累积剂量治疗的儿童中就有1名最终会发生A-CHF。这是一个极高的风险,它强化了重新评估不同治疗方案中使用的蒽环类药物累积剂量以及确定可在治疗方案中实施的预防A-CHF策略的必要性。