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
[62]   Childhood cancer survival in Europe and the United States [J].
Gatta, G ;
Capocaccia, R ;
Coleman, MP ;
Ries, LAG ;
Berrino, F .
CANCER, 2002, 95 (08) :1767-1772
[63]  
GEETHA A, 1989, Indian Journal of Physiology and Pharmacology, V33, P53
[64]   A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics Adriamycin and daunorubicin [J].
Gewirtz, DA .
BIOCHEMICAL PHARMACOLOGY, 1999, 57 (07) :727-741
[65]  
GIANNI L, 1985, J BIOL CHEM, V259, P6056
[66]   Anthracycline-induced cardiotoxicity in children and young adults [J].
Giantris, A ;
Abdurrahman, L ;
Hinkle, A ;
Asselin, B ;
Lipshultz, SE .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 1998, 27 (01) :53-68
[67]   Randomized phase III trial of liposomal daunorubicin versus doxorubicin, bleomycin, and vincristine in AIDS-related Kaposi's sarcoma [J].
Gill, PS ;
Wernz, J ;
Scadden, DT ;
Cohen, P ;
Mukwaya, GM ;
vonRoenn, JH ;
Jacobs, M ;
Kempin, S ;
Silverberg, I ;
Gonzales, G ;
Rarick, MU ;
Myers, AM ;
Shepherd, F ;
Sawka, C ;
Pike, MC ;
Ross, ME .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (08) :2353-2364
[68]   PHASE I/II TRIALS OF WR-2721 AND CISPLATINUM [J].
GLOVER, D ;
GLICK, JH ;
WEILER, C ;
FOX, K ;
TURRISI, A ;
KLIGERMAN, MM .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1986, 12 (08) :1509-1512
[69]   Trace element risk assessment: essentiality vs. toxicity [J].
Goldhaber, SB .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2003, 38 (02) :232-242
[70]   STRUCTURE OF THE ADRIAMYCIN-CARDIOLIPIN COMPLEX - ROLE IN MITOCHONDRIAL TOXICITY [J].
GOORMAGHTIGH, E ;
HUART, P ;
PRAET, M ;
BRASSEUR, R ;
RUYSSCHAERT, JM .
BIOPHYSICAL CHEMISTRY, 1990, 35 (2-3) :247-257