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A Comprehensive Review of Cancer Drug-Induced Cardiotoxicity in Blood Cancer Patients: Current Perspectives and Therapeutic Strategies.
Costanzo, Vincenzo; Ratre, Yashwant Kumar; Andretta, Emanuela; Acharya, Rakesh; Bhaskar, L V K S; Verma, Henu Kumar.
Affiliation
  • Costanzo V; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
  • Ratre YK; Department of Biotechnology, Guru Ghasidas Vishwavidyalaya, Bilaspur, India.
  • Andretta E; Department of Veterinary Medicine and Animal Productions, University of Naples "Federico II", Naples, Italy.
  • Acharya R; Department of Zoology, Guru Ghasidas Vishwavidyalaya, Bilaspur, India.
  • Bhaskar LVKS; Department of Zoology, Guru Ghasidas Vishwavidyalaya, Bilaspur, India.
  • Verma HK; Department of Immunopathology, Institute of Lungs Health and Immunity, Comprehensive Pneumology Center, Helmholtz Zentrum, Neuherberg, 85764, Munich, Germany. henu.verma@yahoo.com.
Curr Treat Options Oncol ; 25(4): 465-495, 2024 04.
Article de En | MEDLINE | ID: mdl-38372853
ABSTRACT
OPINION STATEMENT Cardiotoxicity has emerged as a serious outcome catalyzed by various therapeutic targets in the field of cancer treatment, which includes chemotherapy, radiation, and targeted therapies. The growing significance of cancer drug-induced cardiotoxicity (CDIC) and radiation-induced cardiotoxicity (CRIC) necessitates immediate attention. This article intricately unveils how cancer treatments cause cardiotoxicity, which is exacerbated by patient-specific risks. In particular, drugs like anthracyclines, alkylating agents, and tyrosine kinase inhibitors pose a risk, along with factors such as hypertension and diabetes. Mechanistic insights into oxidative stress and topoisomerase-II-B inhibition are crucial, while cardiac biomarkers show early damage. Timely intervention and prompt treatment, especially with specific agents like dexrazoxane and beta-blockers, are pivotal in the proactive management of CDIC.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs hématologiques / Tumeurs / Antinéoplasiques Limites: Humans Langue: En Journal: Curr Treat Options Oncol / Curr. treat. options oncol / Current treatment options in oncology Sujet du journal: NEOPLASIAS Année: 2024 Type de document: Article Pays d'affiliation: Italie Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs hématologiques / Tumeurs / Antinéoplasiques Limites: Humans Langue: En Journal: Curr Treat Options Oncol / Curr. treat. options oncol / Current treatment options in oncology Sujet du journal: NEOPLASIAS Année: 2024 Type de document: Article Pays d'affiliation: Italie Pays de publication: États-Unis d'Amérique