PMID- 37608525 OWN - NLM STAT- MEDLINE DCOM- 20240308 LR - 20240308 IS - 1744-764X (Electronic) IS - 1474-0338 (Linking) VI - 23 IP - 3 DP - 2024 Mar TI - Cardiovascular toxicities following the use of tyrosine kinase inhibitors in hepatocellular cancer patients: a retrospective, pharmacovigilance study. PG - 287-296 LID - 10.1080/14740338.2023.2251398 [doi] AB - BACKGROUND: Cardiac adverse events (AEs) are common in tyrosine kinase inhibitors(TKIs). This study explored the cardiac AEs of TKIs through the Food and Drug Administration's Adverse Event Reporting System (FAERS). METHODS: Disproportionality analysis and Bayesian analysis were utilized for data mining of the suspected cardiac AEs of TKIs, based on FAERS data from January 2004 to December 2021. RESULTS: A total of 4708 cardiac AEs reports of sorafenib, regorafenib, lenvatinib, and cabozantinib were identified. Hypertension accounts for the most reported cardiac AE. Lenvatinib appears to induce cardiac failure with the highest signals strength [ROR = 7.7 (3.46,17.17)]. Acute myocardial infarction was detected in lenvatinib [ROR = 7.91 (5.64,11.09)] and sorafenib [ROR = 2.22 (1.74, 2.84)]. Acute coronary syndrome was detected in lenvatinib [ROR = 11.57 (6.84, 19.58)] and sorafenib [ROR = 2.81 (1.87,4.24)]. Atrial fibrillation was detected in sorafenib [ROR = 1.82 (1.55,2.14)] and regorafenib [ROR = 1.36 (1.03,1.81)]. Meanwhile, aortic dissections were detected in sorafenib [ROR = 5.08 (3.31,7.8)] and regorafenib [ROR = 3.39 (1.52,7.56)]. Most patients developed hypertension and cardiac failure within 30 days of initiating TKI treatments. Patients taking lenvatinib had an increased incidence of developing acute coronary syndrome after 180 days of treatment. CONCLUSION: Analysis of FAERS data provides a precise profile on the characteristics of cardiac AEs associated with different TKI regimens. Distinct monitoring and appropriate management are needed in the care of TKI recipients. FAU - Lai, Xin AU - Lai X AUID- ORCID: 0009-0004-0288-3043 AD - Department of Pharmacy, First Affiliated Hospital of Nanchang University, Nanchang, China. FAU - Wan, Qing AU - Wan Q AD - Department of Pharmacy, First Affiliated Hospital of Nanchang University, Nanchang, China. FAU - Jiao, Shou-Feng AU - Jiao SF AD - Department of Pharmacy, First Affiliated Hospital of Nanchang University, Nanchang, China. FAU - Sun, Xiao-Chun AU - Sun XC AD - Department of Pharmacy, First Affiliated Hospital of Nanchang University, Nanchang, China. FAU - Hu, Jin-Fang AU - Hu JF AD - Department of Pharmacy, First Affiliated Hospital of Nanchang University, Nanchang, China. FAU - Peng, Hong-Wei AU - Peng HW AD - Department of Pharmacy, First Affiliated Hospital of Nanchang University, Nanchang, China. LA - eng PT - Journal Article DEP - 20230829 PL - England TA - Expert Opin Drug Saf JT - Expert opinion on drug safety JID - 101163027 RN - 24T2A1DOYB (regorafenib) RN - EE083865G2 (lenvatinib) RN - 0 (Tyrosine Kinase Inhibitors) RN - 9ZOQ3TZI87 (Sorafenib) RN - 0 (Phenylurea Compounds) RN - 0 (Pyridines) RN - 0 (Quinolines) SB - IM MH - United States MH - Humans MH - Tyrosine Kinase Inhibitors MH - *Acute Coronary Syndrome MH - Sorafenib/adverse effects MH - Retrospective Studies MH - Bayes Theorem MH - *Carcinoma, Hepatocellular/drug therapy MH - Pharmacovigilance MH - *Liver Neoplasms/drug therapy MH - *Heart Failure MH - *Hypertension MH - United States Food and Drug Administration MH - Adverse Drug Reaction Reporting Systems MH - *Phenylurea Compounds MH - *Pyridines MH - *Quinolines OTO - NOTNLM OT - Cardiac adverse events OT - data mining OT - hepatocellular cancer OT - non-proportional analysis OT - tyrosine kinases inhibitors EDAT- 2023/08/23 06:42 MHDA- 2024/03/08 06:42 CRDT- 2023/08/23 01:13 PHST- 2024/03/08 06:42 [medline] PHST- 2023/08/23 06:42 [pubmed] PHST- 2023/08/23 01:13 [entrez] AID - 10.1080/14740338.2023.2251398 [doi] PST - ppublish SO - Expert Opin Drug Saf. 2024 Mar;23(3):287-296. doi: 10.1080/14740338.2023.2251398. Epub 2023 Aug 29.