Major Adverse Cardiovascular Events in Patients With Renal Cell Carcinoma Treated With Targeted Therapies

被引:15
|
作者
Chen, Dong-Yi [1 ]
Liu, Jia-Rou [2 ]
Tseng, Chi-Nan [3 ]
Hsieh, Ming-Jer [1 ]
Chuang, Cheng-Keng [4 ]
Pang, See-Tong [4 ]
Chen, Shao-Wei [3 ]
Hsieh, I-Chang [1 ]
Chu, Pao-Hsien [1 ]
Chen, Jen-Shi [5 ]
Chang, John Wen-Cheng [5 ]
Huang, Wen-Kuan [5 ,6 ,9 ]
See, Lai-Chu [2 ,7 ,8 ,10 ]
机构
[1] Chang Gung Univ, Chang Gung Mem Hosp Linkou, Dept Internal Med, Div Cardiol,Coll Med, Taoyuan, Taiwan
[2] Chang Gung Univ, Coll Med, Dept Publ Hlth, Taoyuan, Taiwan
[3] Chang Gung Univ, Chang Gung Mem Hosp Linkou, Dept Thorac & Cardiovasc Surg, Coll Med, Taoyuan, Taiwan
[4] Chang Gung Univ, Chang Gung Mem Hosp Linkou, Coll Med, Dept Surg,Div Urol, Taoyuan, Taiwan
[5] Chang Gung Univ, Chang Gung Mem Hosp Linkou, Coll Med, Dept Internal Med,Div Hematol Oncol, Taoyuan, Taiwan
[6] Karolinska Inst, Dept Oncol Pathol, Stockholm, Sweden
[7] Chang Gung Univ, Mol Med cine Res Ctr, Biostat Core Lab, Taoyuan, Taiwan
[8] Chang Gung Mem Hosp Linkou, Dept Internal Med, Div Rheumatol Allergy & Immunol, Taoyuan, Taiwan
[9] Chang Gung Univ, Chang Gung Mem Hosp Linkou, Coll Med, Dept Internal Med,Div Hematol Oncol, 5 Fu Hsing St, Taoyuan 33305, Taiwan
[10] Chang Gung Univ, Coll Med, Dept Publ Hlth, 259 Wenhua 1st Rd, Taoyuan City 33302, Taiwan
来源
JACC: CARDIOONCOLOGY | 2022年 / 4卷 / 02期
关键词
KEY WORDS cardiovascular toxicity; renal; cell carcinoma; targeted cancer therapy; PROPENSITY SCORE METHODS; INTERFERON-ALPHA; RISK; CANCER; HYPERTENSION; SUNITINIB; TOXICITY; MODEL;
D O I
10.1016/j.jaccao.2022.05.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND The risk for major adverse cardiovascular events (MACE) with targeted therapies for patients with advanced renal cell carcinoma (RCC) in real-world practice remains unclear. OBJECTIVES The aim of this study was to compare the risk for MACE associated with targeted cancer therapies with that associated with cytokine treatment in patients with advanced RCC. METHODS Using Taiwan's National Health Insurance Research Database, a retrospective nationwide cohort study was conducted involving patients with advanced RCC who had received targeted therapy (sunitinib, sorafenib, pazopanib, everolimus, or temsirolimus) or cytokine therapy (interleukin-2 or interferon gamma) from 2007 to 2018. Cox proportional hazards models were used to estimate the risk for MACE (a composite of myocardial infarction, ischemic stroke, heart failure, and cardiovascular death) in the cohort using the propensity score method of stabilized inverse probability of treatment weighting. RESULTS In this cohort of 2,785 patients with advanced RCC, 2,257 (81%) and 528 (19%) had received targeted and cytokine therapy, respectively. After stabilized inverse probability of treatment weighting, the incidence rates of MACE were 6.65 and 3.36 per 100 person-years in the targeted and cytokine therapy groups, respectively (HR: 1.80; 95% CI: 1.19-2.74). Baseline history of heart failure (HR: 3.88; 95% CI: 2.25-6.71), atrial fibrillation (HR: 3.60; 95% CI: 2.16-5.99), venous thromboembolism (HR: 2.50; 95% CI: 1.27-4.92), ischemic stroke (HR: 1.88; 95% CI: 1.14-3.11), and age $ 65 years (HR: 1.81; 95% CI: 1.27-2.58) were independent risk factors for targeted therapy-associated MACE. CONCLUSIONS Among patients with advanced RCC, the risk for MACE associated with targeted cancer therapy is higher than that associated with cytokine therapy. (J Am Coll Cardiol CardioOnc 2022;4:223-234) (c) 2022 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:223 / 234
页数:12
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