Anthracycline-Induced Cardiomyopathy in Cancer Survivors: Management and Long-Term Implications.
Seyed Abolfazl MohsenizadehMohsen RajaeinejadMehran KhoshfetratReza ArefizadehSeyed Hossein MousaviReza MosaedMohammad Hassan Kazemi-GalougahiHasan JalaeikhooAli FaridfarMohsen NikandishSepideh Alavi-MoghadamBabak ArjmandPublished in: Advances in experimental medicine and biology (2024)
Recent advancements in personalized treatments, such as anthracycline chemotherapy, coupled with timely diagnoses, have contributed to a decrease in cancer-specific mortality rates and an improvement in cancer prognosis. Anthracyclines, a potent class of antibiotics, are extensively used as anticancer medications to treat a broad spectrum of tumors. Despite these advancements, a considerable number of cancer survivors face increased risks of treatment complications, particularly the cardiotoxic effects of chemotherapeutic drugs like anthracyclines. These effects can range from subclinical manifestations to severe consequences such as irreversible heart failure and death, highlighting the need for effective management of chemotherapy side effects for improved cancer care outcomes. Given the lack of specific treatments, early detection of subclinical cardiac events post-anthracycline therapy and the implementation of preventive strategies are vital. An interdisciplinary approach involving cardiovascular teams is crucial for the prevention and efficient management of anthracycline-induced cardiotoxicity. Various factors, such as age, gender, duration of treatment, and comorbidities, should be considered significant risk factors for developing chemotherapy-related cardiotoxicity. Tools such as electrocardiography, echocardiography, nuclear imaging, magnetic resonance imaging, histopathologic evaluations, and serum biomarkers should be appropriately used for the early detection of anthracycline-related cardiotoxicity. Furthermore, understanding the underlying biological mechanisms is key to developing preventive measures and personalized treatment strategies to mitigate anthracycline-induced cardiotoxicity. Exploring specific cardiotoxic mechanisms and identifying genetic variations can offer fresh perspectives on innovative, personalized treatments. This chapter aims to discuss cardiomyopathy following anthracycline therapy, with a focus on molecular mechanisms, preventive strategies, and emerging treatments.
Keyphrases
- heart failure
- high glucose
- magnetic resonance imaging
- drug induced
- diabetic rats
- left ventricular
- papillary thyroid
- young adults
- computed tomography
- childhood cancer
- healthcare
- squamous cell
- locally advanced
- primary care
- squamous cell carcinoma
- radiation therapy
- climate change
- mental health
- metabolic syndrome
- coronary artery disease
- endothelial cells
- risk factors
- dna methylation
- cardiovascular events
- cardiovascular disease
- oxidative stress
- combination therapy
- skeletal muscle
- acute heart failure
- photodynamic therapy
- chemotherapy induced
- lymph node metastasis
- contrast enhanced
- stress induced