Research Progress on the Cardiotoxicity of EGFR-TKIs in Non-Small Cell Lung Cancer

被引:1
作者
Yu, Yinan [1 ]
Zhao, Jianguo [1 ]
Xu, Jiaona [2 ]
Bai, Rui [3 ]
Gu, Zewei [4 ]
Chen, Xialin [1 ]
Wang, Jianfang [1 ]
Jin, Xueying [1 ]
Gu, Gaoyang [5 ]
机构
[1] Shaoxing Peoples Hosp, Dept Oncol, Shaoxing, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hangzhou Peoples Hosp 1, Dept Rehabil, Sch Med, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Oncol, Hangzhou, Zhejiang, Peoples R China
[4] Hangzhou Med Coll, Sch Clin Med, Hangzhou, Zhejiang, Peoples R China
[5] First Peoples Hosp Huzhou, Dept Cardiol, 158 Plaza Back Rd, Huzhou 313000, Zhejiang, Peoples R China
关键词
Cardiotoxicity; Epidermal growth factor receptor; Non-small cell lung cancer; Tyrosine kinase inhibitor; OSIMERTINIB-INDUCED CARDIOTOXICITY; ADVERSE EVENTS; HEART-FAILURE; ERLOTINIB; CARDIOMYOPATHY; ADENOCARCINOMA; INHIBITOR;
D O I
10.1007/s11864-023-01150-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
With the development of molecular biology and histology techniques, targeted therapy for non-small cell lung cancer (NSCLC) has emerged, which is highly effective and has marginal side effects. Epidermal growth factor receptor (EGFR) was the first driver gene discovered, whose three generations of therapeutic use have its characteristics and benefits in clinical practice. However, cardiovascular complications by EGFR-tyrosine kinase inhibitors (EGFR-TKIs) in preclinical studies have been increasingly reported, including heart failure, cardiomyopathy, and QT prolongation, among others. Cardiotoxicity of targeted drugs significantly affects the therapeutic effect of NSCLC and has become the second leading cause of death in NSCLC. The aim of the present review was to recognize the potential cardiotoxicity of third-generation targeted drugs in the treatment of NSCLC and their associated mechanisms to help clinicians identify and prevent it early in the treatment, minimize the cardiotoxicity of targeted drugs, and improve the therapeutic effect of patients.
引用
收藏
页码:1889 / 1916
页数:28
相关论文
共 44 条
[1]  
Abdelgalil AA, 2020, PROF DRUG SUB EXCIP, V45, P93, DOI 10.1016/bs.podrm.2019.10.004
[2]   Angiotensin II type 1 receptor blockade attenuates gefitinib-induced cardiac hypertrophy via adjusting angiotensin II-mediated oxidative stress and JNK/P38 MAPK pathway in a rat model [J].
Alanazi, Wael A. ;
Alhamami, Hussain N. ;
Alharbi, Metab ;
Alhazzani, Khalid ;
Alanazi, Abdulrahman S. ;
Alsanea, Sary ;
Ali, Nemat ;
Alasmari, Abdullah F. ;
Alanazi, Ahmed Z. ;
Alotaibi, Moureq R. ;
Alswayyed, Mohammed .
SAUDI PHARMACEUTICAL JOURNAL, 2022, 30 (08) :1159-1169
[3]   Liraglutide attenuates gefitinib-induced cardiotoxicity and promotes cardioprotection through the regulation of MAPK/NF-κB signaling pathways [J].
AlAsmari, Abdullah F. ;
Ali, Nemat ;
AlAsmari, Fawaz ;
AlAnazi, Wael A. ;
AlShammari, Musaad A. ;
Al-Harbi, Naif O. ;
Alhoshani, Ali ;
Sobeai, Homood M. As ;
AlSwayyed, Mohammed ;
AlAnazi, Mohammed M. ;
AlGhamdi, Nader S. .
SAUDI PHARMACEUTICAL JOURNAL, 2020, 28 (04) :509-518
[4]   EGFR Inhibitor Gefitinib Induces Cardiotoxicity through the Modulation of Cardiac PTEN/Akt/FoxO3a Pathway and Reactive Metabolites Formation: In Vivo and in Vitro Rat Studies [J].
Alhoshani, Ali ;
Alanazi, Fawaz E. ;
Alotaibi, Moureq R. ;
Attwa, Mohamed W. ;
Kadi, Adnan A. ;
Aldhfyan, Abdullah ;
Akhtar, Sabah ;
Hourani, Shireen ;
Agouni, Abdelali ;
Zeidan, Asad ;
Korashy, Hesham M. .
CHEMICAL RESEARCH IN TOXICOLOGY, 2020, 33 (07) :1719-1728
[5]   Osimertinib-Induced Cardiotoxicity A Retrospective Review of the FDA Adverse Events Reporting System (FAERS) [J].
Anand, Kartik ;
Ensor, Joe ;
Trachtenberg, Barry ;
Bernicker, Eric H. .
JACC: CARDIOONCOLOGY, 2019, 1 (02) :172-178
[6]   QT interval prolongation related to afatinib treatment in a patient with metastatic non-small-cell lung cancer [J].
Demircan, Nazim Can ;
Telli, Tugba Akin ;
Tuylu, Tugba Basoglu ;
Arikan, Rukiye ;
Kocakaya, Derya ;
Sahin, Ahmet Anil ;
Ercelep, Ozlem ;
Dane, Faysal ;
Yumuk, Perran Fulden .
CURRENT PROBLEMS IN CANCER, 2020, 44 (06)
[7]   Acute myocardial infarction following erlotinib treatment for NSCLC: A case report [J].
Ding, Shanshan ;
Long, Fei ;
Jiang, Shujuan .
ONCOLOGY LETTERS, 2016, 11 (06) :4240-4244
[8]   Multi-parameter in vitro toxicity testing of crizotinib, sunitinib, erlotinib, and nilotinib in human cardiomyocytes [J].
Doherty, Kimberly R. ;
Wappel, Robert L. ;
Talbert, Dominique R. ;
Trusk, Patricia B. ;
Moran, Diarmuid M. ;
Kramer, James W. ;
Brown, Arthur M. ;
Shell, Scott A. ;
Bacus, Sarah .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2013, 272 (01) :245-255
[9]   Tyrosine kinase-targeting drugs-associated heart failure [J].
Gronich, N. ;
Lavi, I. ;
Barnett-Griness, O. ;
Saliba, W. ;
Abernethy, D. R. ;
Rennert, G. .
BRITISH JOURNAL OF CANCER, 2017, 116 (10) :1366-1373
[10]   Adverse cardiac effects of cancer therapies: cardiotoxicity and arrhythmia [J].
Herrmann, Joerg .
NATURE REVIEWS CARDIOLOGY, 2020, 17 (08) :474-502