Literature DB >> 17652803

The anthracyclines: when good things go bad.

Giorgio Minotti, Narine Sarvazyan.   

Abstract

In the era of targeted therapy the anthracyclines, which were discovered almost half-century ago, may appear to be too old to be good. While it is certainly true that the prototypic anthracyclines have been around for many years, there are robust clinical facts to confute that their time is over. These drugs continue to play an undisputed role in the treatment of many forms of cancer, including hematological malignancies and solid tumors. Unfortunately, however, their main side-effect remains: a life-threatening cardiotoxicity which became apparent at the beginning of anthracyclines' clinical use. In addition to this long-standing problem, we are now discovering that new combination therapies often cause a higher than expected incidence of cardiotoxicity, as if the newly designed drugs make the heart more vulnerable to the old one. Altogether, however, an overwhelming amount of clinical evidence suggests that anthracyclines are too good to be old. Yet, they would look much better if they caused less harm to the heart when administered as either single agents or in combination with otherwise promising new drugs.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17652803      PMCID: PMC3019579          DOI: 10.1007/s12012-007-0017-1

Source DB:  PubMed          Journal:  Cardiovasc Toxicol        ISSN: 1530-7905            Impact factor:   3.231


  19 in total

Review 1.  Anthracycline cardiotoxicity in breast cancer patients: synergism with trastuzumab and taxanes.

Authors:  Luca Gianni; Emanuela Salvatorelli; Giorgio Minotti
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

Review 2.  Cardiac safety of liposomal anthracyclines.

Authors:  Gerald Batist
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

Review 3.  Antioxidant defense against anthracycline cardiotoxicity by metallothionein.

Authors:  Y James Kang
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

Review 4.  Ongoing phase I and II studies of novel anthracyclines.

Authors:  Cristiana Sessa; Olga Valota; Cristina Geroni
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

Review 5.  Role of anthracyclines in the era of targeted therapy.

Authors:  Hernán Cortés-Funes; Cyntia Coronado
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

Review 6.  An introduction to the metabolic determinants of anthracycline cardiotoxicity.

Authors:  Pierantonio Menna; Stefania Recalcati; Gaetano Cairo; Giorgio Minotti
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

Review 7.  Anthracycline-induced phospholipase A2 inhibition.

Authors:  Luther Swift; Jane McHowat; Narine Sarvazyan
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

Review 8.  Role of mtDNA lesions in anthracycline cardiotoxicity.

Authors:  Dirk Lebrecht; Ulrich A Walker
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

Review 9.  Adriamycin-induced interference with cardiac mitochondrial calcium homeostasis.

Authors:  Kendall B Wallace
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

Review 10.  Novel antioxidants in anthracycline cardiotoxicity.

Authors:  Kálmán Hideg; Tamás Kálai
Journal:  Cardiovasc Toxicol       Date:  2007       Impact factor: 3.231

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.