Protecting against anthracycline-induced myocardial damage: a review of the most promising strategies

被引:303
作者
Wouters, KA
Kremer, LCM
Miller, TL
Herman, EH
Lipshultz, SE
机构
[1] Vrije Univ Amsterdam, Med Ctr, Div Pediat, Amsterdam, Netherlands
[2] Emma Childrens Hosp, Dept Paediat Oncol, Acad Med Ctr, Amsterdam, Netherlands
[3] Univ Miami, Miller Sch Med, Div Pediat Clin Res, Miami, FL 33152 USA
[4] US FDA, Ctr Drug Evaluat & Res, Div Appl Pharmacol Res, Silver Spring, MD USA
[5] Univ Miami, Jackson Mem Med Ctr, Holtz Childrens Hosp, Miami, FL 33152 USA
[6] Univ Miami, Sylvester Comprehens Canc Ctr, Miami, FL 33152 USA
关键词
cancer; anthracyclines; myocardial damage; cardioprotective agents; prevention;
D O I
10.1111/j.1365-2141.2005.05759.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Over the last 40 years, great progress has been made in treating childhood and adult cancers. However, this progress has come at an unforeseen cost, in the form of emerging long-term effects of anthracycline treatment. A major complication of anthracycline therapy is its adverse cardiovascular effects. If these cardiac complications could be reduced or prevented, higher doses of anthracyclines could potentially be used, thereby further increasing cancer cure rates. Moreover, as the incidence of cardiac toxicity resulting in congestive heart failure or even heart transplantation dropped, the quality and extent of life for cancer survivors would improve. We review the proposed mechanisms of action of anthracyclines and the consequences associated with anthracycline treatment in children and adults. We summarise the most promising current strategies to limit or prevent anthracycline-induced cardiotoxicity, as well as possible strategies to prevent existing cardiomyopathy from worsening.
引用
收藏
页码:561 / 578
页数:18
相关论文
共 208 条
[1]   Acute and chronic effects of adriamycin on fatty acid oxidation in isolated cardiac myocytes [J].
AbdelAleem, S ;
ElMerzabani, MM ;
SayedAhmed, M ;
Taylor, DA ;
Lowe, JE .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (02) :789-797
[2]   Pathophysiology of anthracycline- and radiation-associated card iomyopathies: Implications for screening and prevention [J].
Adams, MJ ;
Lipshultz, SE .
PEDIATRIC BLOOD & CANCER, 2005, 44 (07) :600-606
[3]  
ALDERTON PM, 1992, CANCER RES, V52, P194
[4]   IDARUBICIN CARDIOTOXICITY - A RETROSPECTIVE STUDY IN ACUTE MYELOID-LEUKEMIA AND MYELODYSPLASIA [J].
ANDERLINI, P ;
BENJAMIN, RS ;
WONG, FC ;
KANTARJIAN, HM ;
ANDREEFF, M ;
KORNBLAU, SM ;
OBRIEN, S ;
MACKAY, B ;
EWER, MS ;
PIERCE, SA ;
ESTEY, EH .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (11) :2827-2834
[5]  
[Anonymous], 1992, NEW ENGL J MED, V327, P685, DOI [DOI 10.1056/NEJM199209033271003, 10.1056/NEJM199209033271003.Erratumin]
[6]  
[Anonymous], 2001, DIET REF INT VIT A V
[7]  
[Anonymous], LATE EFFECTS CHILDHO
[8]  
[Anonymous], ABSORPTION UTILIZATI
[9]  
Antunes LMG, 1999, TERATOGEN CARCIN MUT, V19, P53
[10]   Mechanism of doxorubicin-induced inhibition of sarcoplasmic reticulum Ca2+-ATPase gene transcription [J].
Arai, M ;
Yoguchi, A ;
Takizawa, T ;
Yokoyama, T ;
Kanda, T ;
Kurabayashi, M ;
Nagai, R .
CIRCULATION RESEARCH, 2000, 86 (01) :8-14