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This document discusses cardiotoxicity caused by various antineoplastic drugs and defines two main types of drug-induced cardiomyopathy - Type I caused by anthracyclines and Type II caused by trastuzumab. It describes the short-term and long-term effects of Type I agents as well as risk factors and pathophysiological mechanisms. For Type II agents, it covers risk factors and mechanisms including interaction with anthracyclines. The document also briefly mentions other cardiotoxic effects, strategies to limit toxicity, and techniques for monitoring cardiotoxicity in clinical practice.
This document discusses cardiotoxicity caused by various antineoplastic drugs and defines two main types of drug-induced cardiomyopathy - Type I caused by anthracyclines and Type II caused by trastuzumab. It describes the short-term and long-term effects of Type I agents as well as risk factors and pathophysiological mechanisms. For Type II agents, it covers risk factors and mechanisms including interaction with anthracyclines. The document also briefly mentions other cardiotoxic effects, strategies to limit toxicity, and techniques for monitoring cardiotoxicity in clinical practice.
This document discusses cardiotoxicity caused by various antineoplastic drugs and defines two main types of drug-induced cardiomyopathy - Type I caused by anthracyclines and Type II caused by trastuzumab. It describes the short-term and long-term effects of Type I agents as well as risk factors and pathophysiological mechanisms. For Type II agents, it covers risk factors and mechanisms including interaction with anthracyclines. The document also briefly mentions other cardiotoxic effects, strategies to limit toxicity, and techniques for monitoring cardiotoxicity in clinical practice.
Definition of cardiotoxicity Antineoplastic drugs and cardiomyopathy
Type I agents: anthracyclines
Short- and long-term cardiotoxic effects Risk factors Pathophysiological mechanisms 2 Strategies to limit cardiotoxicity
Type II agents: trastuzumab
Risk factors Pathophysiological mechanisms 3 a)
Anthracyclines, hypoxia, oxidative stress
b) Anthracyclines, hypoxia, oxidative stress
Cardiotoxicity of concomitant trastuzumab and anthracyclines 4 Figure 2 Interaction of the cardiotoxic mechanisms of anthracyclines with those of trastuzumab.
Strategies to limit cardiotoxicity 5
Other cardiotoxic effects
Myocardial ischemia
Arrhythmias Systemic hypertension Thromboembolism
Cardiotoxicity associated with radiotherapy 6
Table 4 Cardiotoxicity of the main classes of cancer drugs used in clinical practice. 7 (2 hojas) Table 5 Advantages and disadvantages of the principal techniques used for monitoring cardiotoxicity in clinical practice. 8 (2 hojas)