Cardiometabolic Consequences of Targeted Anticancer Therapies

被引:1
作者
Guha, Avirup [1 ,2 ]
Gong, Yan [3 ]
DeRemer, David [3 ]
Owusu-Guha, Jocelyn [4 ]
Dent, Susan F. [5 ]
Cheng, Richard K. [6 ]
Weintraub, Neal L. [2 ,7 ]
Agarwal, Neeraj [8 ]
Fradley, Michael G. [8 ]
机构
[1] Case Western Reserve Univ, Harrington Heart & Vasc Inst, 11100 Euclid Ave, Cleveland, OH 44106 USA
[2] Augusta Univ, Div Cardiol, Dept Med, Augusta, GA USA
[3] Univ Florida, Dept Pharmacotherapy & Translat Res, Coll Pharm, Ctr Pharmacogen & Precis Med, Gainesville, FL USA
[4] Riverside Methodist Hosp, Dept Pharm, Columbus, OH USA
[5] Duke Univ, Duke Canc Inst, Durham, NC USA
[6] Augusta Univ, Vasc Biol Ctr, Augusta, GA USA
[7] Univ Utah NCI CCC, Huntsman Canc Inst, Salt Lake City, UT USA
[8] Univ Penn, Div Cardiol, Dept Med, Philadelphia, PA USA
关键词
cardio-oncology; cardiometabolic disease; diabetes; hypertension; anticancer therapy; ANDROGEN DEPRIVATION THERAPY; RENAL-TRANSPLANT RECIPIENTS; CHRONIC MYELOID-LEUKEMIA; MYCOPHENOLATE-MOFETIL; RISK-FACTORS; EVEROLIMUS; SIROLIMUS; EFFICACY; CANCER; METABOLISM;
D O I
10.1097/FJC.0000000000001149
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiometabolic disease (CMD) is the most common preventable cause of death in the world. A number of components are included in the spectrum of CMD, such as metabolic syndrome/obesity, hyperglycemia/diabetes, dyslipidemia, and hypertension, which are independently associated with cardiovascular disease risk. These conditions often occur together, and patients with cancer frequently undergo treatments that can generate or worsen CMD. This review highlights and presents mechanistic and epidemiological evidence regarding CMD in 4 categories of anticancer medications, namely, mTOR/PI3K-Akt inhibitors, multitargeted tyrosine kinase inhibitor, immune checkpoint inhibitor therapy, and endocrine therapy. Patients taking these medications need careful monitoring during therapy. There is a role for cardio-oncology and onco-primary care specialists in optimally managing patients at risk to mitigate CMD during treatment with these and other investigational anticancer medications.
引用
收藏
页码:515 / 521
页数:7
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