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Absence of secondary malignant neoplasms in children with high-risk acute lymphoblastic leukemia treated with dexrazoxane.接受右丙亚胺治疗的高危急性淋巴细胞白血病儿童未发生继发性恶性肿瘤。
J Clin Oncol. 2008 Mar 1;26(7):1106-11. doi: 10.1200/JCO.2007.12.2481.
2
Daunorubicin-induced cell kill with 1-hour versus 24-hour infusions: a randomized comparison in children with newly diagnosed acute lymphoblastic leukemia.柔红霉素1小时输注与24小时输注诱导的细胞杀伤作用:新诊断急性淋巴细胞白血病儿童的随机对照研究
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Clinical and cost-effectiveness of cardioprotection against the toxic effects of anthracyclines given to children with cancer: a systematic review.针对癌症患儿使用蒽环类药物毒性的心脏保护的临床疗效及成本效益:一项系统评价
Br J Cancer. 2007 Jan 29;96(2):226-30. doi: 10.1038/sj.bjc.6603562.
4
Different dosage schedules for reducing cardiotoxicity in cancer patients receiving anthracycline chemotherapy.在接受蒽环类化疗的癌症患者中降低心脏毒性的不同给药方案。
Cochrane Database Syst Rev. 2006 Oct 18(4):CD005008. doi: 10.1002/14651858.CD005008.pub2.
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Different anthracycline derivates for reducing cardiotoxicity in cancer patients.用于降低癌症患者心脏毒性的不同蒽环类衍生物。
Cochrane Database Syst Rev. 2006 Oct 18(4):CD005006. doi: 10.1002/14651858.CD005006.pub2.
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Clinical heart failure in a cohort of children treated with anthracyclines: a long-term follow-up study.一组接受蒽环类药物治疗儿童的临床心力衰竭:一项长期随访研究。
Eur J Cancer. 2006 Dec;42(18):3191-8. doi: 10.1016/j.ejca.2006.08.005. Epub 2006 Sep 20.
7
Exposure to anthracyclines during childhood causes cardiac injury.儿童时期接触蒽环类药物会导致心脏损伤。
Semin Oncol. 2006 Jun;33(3 Suppl 8):S8-14. doi: 10.1053/j.seminoncol.2006.04.019.
8
Pathogenesis of cardiotoxicity induced by anthracyclines.蒽环类药物所致心脏毒性的发病机制。
Semin Oncol. 2006 Jun;33(3 Suppl 8):S2-7. doi: 10.1053/j.seminoncol.2006.04.020.
9
Cardioprotective interventions for cancer patients receiving anthracyclines.针对接受蒽环类药物治疗的癌症患者的心脏保护干预措施。
Cochrane Database Syst Rev. 2005 Jan 25(1):CD003917. doi: 10.1002/14651858.CD003917.pub2.
10
The effect of dexrazoxane on myocardial injury in doxorubicin-treated children with acute lymphoblastic leukemia.右丙亚胺对多柔比星治疗的急性淋巴细胞白血病儿童心肌损伤的影响。
N Engl J Med. 2004 Jul 8;351(2):145-53. doi: 10.1056/NEJMoa035153.

蒽环类药物治疗儿童急性淋巴细胞白血病的有益和有害影响:一项系统评价和荟萃分析。

Beneficial and harmful effects of anthracyclines in the treatment of childhood acute lymphoblastic leukaemia: a systematic review and meta-analysis.

机构信息

CALLCG secretariat, Richard Doll Building, University of Oxford, Roosevelt Drive, Oxford, UK.

出版信息

Br J Haematol. 2009 May;145(3):376-88. doi: 10.1111/j.1365-2141.2009.07624.x. Epub 2009 Feb 22.

DOI:10.1111/j.1365-2141.2009.07624.x
PMID:19236609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2812732/
Abstract

Anthracyclines are used to treat childhood acute lymphoblastic leukaemia (ALL) but non-randomized studies suggest that cardiotoxicity may be a problem. Individual patient data from trials in childhood ALL that randomized anthracyclines or methods of reducing cardiotoxicity were analysed by standard meta-analysis methods. Results were grouped and combined according to: addition of an anthracycline to standard therapy, type of anthracycline, mode of administration, and the use of a cardioprotectant. Data from 958 patients in 4 trials, recruiting between 1972 and 1984, showed that addition of an anthracycline reduced bone marrow relapse and, non-significantly, non-bone marrow relapse, resulting in an increased relapse-free interval. However there was a non-significant increase in induction failures, and in deaths in first remission. Event-free survival at 5 years was 56.7% with anthracycline versus 52.8% without (Odds Ratio = 0.91; 95% Confidence Interval = 0.76-1.10; P = 0.3). There were no significant differences found in other treatment comparisons. The limited data from trials did not demonstrate differences in clinically evident cardiotoxicity. Anthracyclines are effective against bone marrow relapse but have not been shown to significantly increase event free survival in childhood ALL. The evidence on type of anthracycline, method of administration or use of cardioprotectant was insufficient to be able to rule out important differences.

摘要

蒽环类药物用于治疗儿童急性淋巴细胞白血病(ALL),但非随机研究表明心脏毒性可能是个问题。采用标准荟萃分析方法,对儿童ALL试验中随机使用蒽环类药物或降低心脏毒性方法的个体患者数据进行了分析。结果根据以下因素进行分组和合并:在标准治疗中添加蒽环类药物、蒽环类药物的类型、给药方式以及使用心脏保护剂。1972年至1984年间招募的4项试验中958名患者的数据显示,添加蒽环类药物可降低骨髓复发率,对非骨髓复发率的降低无显著影响,从而延长无复发生存期。然而,诱导失败和首次缓解期死亡人数有非显著增加。使用蒽环类药物时5年无事件生存率为56.7%,未使用时为52.8%(优势比 = 0.91;95%置信区间 = 0.76 - 1.10;P = 0.3)。在其他治疗比较中未发现显著差异。试验中的有限数据未显示出临床明显心脏毒性的差异。蒽环类药物对骨髓复发有效,但尚未证明能显著提高儿童ALL的无事件生存率。关于蒽环类药物的类型、给药方法或心脏保护剂使用的证据不足以排除重要差异。