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Prophylactic Agents for Preventing Cardiotoxicity Induced Following Anticancer Agents: A Systematic Review and Meta-Analysis of Clinical Trials Publisher Pubmed



Keshavarzian E1 ; Sadighpour T2, 3 ; Mortazavizadeh SM4 ; Soltani M5 ; Motevalipoor AF6 ; Khamas SS7 ; Moazen M8 ; Kogani M9 ; Hashemipour SMA10 ; Hosseinpour H11 ; Valizadeh R11
Authors
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Authors Affiliations
  1. 1. Health Care Center of Karun, Ahwaz Jondishapur University of Medical Science, Ahwaz, Iran
  2. 2. Herbert Wertheim College of Medicine, Florida International University, Florida, 33199, FL, United States
  3. 3. American University of Antigua College of Medicine, Osbourn, Antigua and Barbuda
  4. 4. Department of Clinical Oncology, Yazd Branch, Islamic Azad University, Yazd, Iran
  5. 5. Yazd Cardiovascular Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
  6. 6. Department of Biotechnology, Yazd Branch, Islamic Azad University, Yazd, Iran
  7. 7. School of Pharmacy, Guilan University of Medical Sciences, Rasht, Iran
  8. 8. Department of Pharmacoeconomics and Pharmaceutical Administration, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. Research Center for Environmental Contaminants (RCEC), Abadan University of Medical Sciences, Abadan, Iran
  10. 10. Young Researchers and Elites Club, Faculty of Medicine, Islamic Azad University, Yazd Branch, Yazd, Iran
  11. 11. Urmia University of Medical Sciences, Urmia, Iran

Source: Reviews on Recent Clinical Trials Published:2023


Abstract

Background: Anthracyclines can improve survival in many types of malignancies, but dose-dependent and irreversible results following the use of anthracyclines have been associated with cardiomyopathy. This meta-analysis aimed to compare the effects of prophylactic agents for preventing cardiotoxicity induced following anticancer agents. Methods: In this meta-analysis, Scopus, Web of Science, and PubMed were surfed for articles published by December 30th, 2020. The keywords were angiotensin‐converting enzyme inhibitor (ACEI), enalapril, captopril, angiotensin receptor blocker, beta blocker, metoprolol, bisoprolol, isoprolol, statin, valsartan, losartan, eplerenone, idarubicin, nebivolol, dihydromyricetin, ampelopsin, spironolactone, dexrazoxane, antioxidants, cardiotoxicity, n-acetyl-tryptamine, cancer, neoplasms, chemotherapy, anthracyclines, doxorubicin, daunorubicin, epirubicin, idarubicin, ejection fraction or a combination of them in the titles or abstracts. Results: A total of 17 articles out of 728 studies examining 2,674 patients were included in this systematic review and meta-analysis. Ejection fraction (EF) values in the baseline, 6-month, and 12-month follow-up in the intervention group turned out to be 62.52 ± 2.48, 59.63 ± 4.85, and 59.42 ± 4.53, whereas in the control group appeared to be 62.81 ± 2.58, 57.69 ± 4.32, and 58.60 ± 4.58, respectively. Through comparison of the two groups, EF was found to increase in the intervention group by 0.40 after 6 months (Standardized mean difference (SMD): 0.40, 95% confidence interval (CI): 0.27, 0.54), thus proving higher than that of the control groups following the cardiac drugs. Conclusion: This meta-analysis showed that prophylactic treatment with cardio-protective drugs, including dexrazoxane, beta blocker, and ACEI drugs in patients undergoing chemotherapy with anthracycline, have a protective effect on LVEF and prevent EF drop. © 2023 Bentham Science Publishers.
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