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蒽环类药物心脏毒性的发生率和临床预测因素的回顾性分析和荟萃分析。

Review and meta-analysis of incidence and clinical predictors of anthracycline cardiotoxicity.

机构信息

Heart Failure and Cardiac Rehabilitation Unit, Catholic University of the Sacred Heart, Rome, Italy.

出版信息

Am J Cardiol. 2013 Dec 15;112(12):1980-4. doi: 10.1016/j.amjcard.2013.08.026. Epub 2013 Sep 25.

Abstract

The management of individual patients requiring anthracyclines remains challenging because uncertainty persists on predictors of cardiotoxicity. We aimed to perform a systematic review and meta-analysis on incidence and predictors of anthracycline chemotherapy in patients with cancer. Databases were searched for pertinent studies. Meta-analytic pooling with random-effects methods was performed for incidence estimates, while relying on descriptive statistics for prevalence and strength of association of predictors. From 16,054 retrieved citations, 18 studies reporting on 49,017 patients with cancer were included, with 22,815 treated with anthracyclines. After a median follow-up of 9 years, clinically overt cardiotoxicity occurred in 6% (95% confidence interval 3% to 9%), whereas subclinical cardiotoxicity developed in 18% (95% confidence interval 12% to 24%). Appraisal of independent risk factors of cardiotoxicity showed that cumulative anthracycline dose was most consistently reported as an accurate and robust predictor of cardiotoxicity, with an acceptable prognostic role also for chest radiotherapy, African-American ethnicity, very young or very old age, diabetes, hypertension, very high or very low body weight, or severe co-morbidities. In conclusion, despite ongoing refinements in chemotherapy regimens, anthracyclines still pose a significant risk of cardiotoxicity, especially in those requiring a high cumulative dose or chest radiotherapy.

摘要

对于需要使用蒽环类药物的个体患者的管理仍然具有挑战性,因为对于心脏毒性的预测因素仍存在不确定性。我们旨在对癌症患者接受蒽环类化疗的发生率和预测因素进行系统评价和荟萃分析。检索了数据库中相关的研究。采用随机效应方法进行荟萃分析以估算发生率,同时依靠描述性统计来评估预测因素的流行率和关联强度。从 16054 篇检索文献中,纳入了 18 项研究,共纳入了 49017 例癌症患者,其中 22815 例接受了蒽环类药物治疗。中位随访 9 年后,临床明显的心脏毒性发生率为 6%(95%置信区间 3%至 9%),而亚临床心脏毒性发生率为 18%(95%置信区间 12%至 24%)。评估心脏毒性的独立危险因素表明,累积蒽环类药物剂量是最一致的心脏毒性预测因素,具有良好的预测作用,胸部放疗、非裔美国人种族、非常年轻或非常年长、糖尿病、高血压、体重过高或过低、或严重合并症也是如此。总之,尽管化疗方案不断改进,但蒽环类药物仍存在显著的心脏毒性风险,尤其是在需要高累积剂量或胸部放疗的患者中。

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