Cardiovascular toxicity following sunitinib therapy in metastatic renal cell carcinoma: a multicenter analysis

被引:165
作者
Di Lorenzo, G. [1 ]
Autorino, R. [2 ]
Bruni, G. [3 ]
Carteni, G. [4 ]
Ricevuto, E. [5 ]
Tudini, M. [5 ]
Ficorella, C. [5 ]
Romano, C. [6 ]
Aieta, M. [6 ]
Giordano, A.
Giuliano, M.
Gonnella, A.
De Nunzio, C. [7 ]
Rizzo, M. [4 ]
Montesarchio, V. [8 ]
Ewer, M. [9 ]
De Placido, S. [1 ]
机构
[1] Univ Naples Federico 2, Dipartimento Endocrinol & Oncol Clin & Mol, Naples, Italy
[2] Univ Naples 2, Urol Clin, Naples, Italy
[3] INT Fdn G Pascale, UOC Oncol, Naples, Italy
[4] Osped Cardarelli, UOC Oncol, Naples, Italy
[5] Univ Aquila, UO Oncol, I-67100 Laquila, Italy
[6] Osped Oncol Reg, UO Oncol, Potenza, Italy
[7] Osped St Andrea, UOC Urol, Rome, Italy
[8] AO Cotugno, UO Oncol, Naples, Italy
[9] Univ Texas MD Anderson Canc Ctr, Dept Cardiol, Houston, TX 77030 USA
关键词
cardiotoxicity; hypertension; metastatic kidney cancer; sunitinib; TYROSINE KINASE INHIBITOR; MONOCLONAL-ANTIBODY; CARDIAC DYSFUNCTION; INTERFERON-ALPHA; CLINICAL-TRIALS; BREAST-CANCER; HEART-FAILURE; CARDIOTOXICITY; CHEMOTHERAPY; MALATE;
D O I
10.1093/annonc/mdp025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients and methods: The medical records of 175 patients with metastatic RCC treated with sunitinib at eight Italian institutions were retrospectively reviewed. Alterations in left ventricular ejection fraction (LVEF) and blood pressure were evaluated. Patients with preexisting cardiac risk factors were specifically scrutinized for increased expression of cardiac changes. Results: Grade 3 hypertension was seen in 17 patients (9.7%); in 12 of these 17, hypertension developed after receiving the third sunitinib cycle. Among these 17 patients, 12 (70.6%) also experienced left ventricular systolic (LVEF) dysfunction; in all, 33 of the 175 patients (18.9%) developed some degree of cardiac abnormality, of which 12 were classified as grade 3 LVEF dysfunction and/or congestive heart failure (CHF) (6.9%). Significant univariate associations for predictors of CHF were history of hypertension (P = 0.008), history of coronary heart disease (P = 0.0005) and prior treatment with an angiotensin-converting enzyme inhibitor (P = 0.04). Multivariate analysis suggested that a history of coronary artery disease [odds ratio (OR) 18, 95% confidence interval (CI) 4-160, P = 0.005] and hypertension (OR 3, 95% CI 1.5-80, P = 0.04) was the only significant independent predictors of CHF. Conclusions: Patients undergoing sunitinib, especially those with a previous history of hypertension and coronary heart disease, are at increased risk for cardiovascular events and should be monitored for exacerbations of their hypertension and for evidence of LVEF dysfunction during treatment.
引用
收藏
页码:1535 / 1542
页数:8
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