Key result
Sunitinib exposure for 40 days in patients with metastatic renal cell carcinoma significantly reduced median flow-mediated dilation from 12.5% to 9.0% (P=0.001), indicating early endothelial dysfunction.
Why the study?
Data available on the effects of sunitinib on endothelial dysfunction, metabolic changes, and cardiovascular risk factors in patients with renal cell carcinoma are limited.
Does sunitinib worsen endothelial dysfunction, metabolic changes, and cardiovascular risk indices in patients with metastatic renal cell carcinoma?
Observational (n=20)
No
Does sunitinib worsen endothelial dysfunction, metabolic changes, and cardiovascular risk indices in patients with metastatic renal cell carcinoma?
Absolute Event Rate: 9% vs 12.5%
p-value: p=0.001
Short-term sunitinib treatment in metastatic renal cell carcinoma induces early markers of endothelial dysfunction, hypertension, and metabolic alterations, highlighting the need for cardiovascular monitoring.
Short-term sunitinib may induce endothelial dysfunction in metastatic RCC; hypothesis-generating for cardiovascular monitoring strategies.
BACKGROUND: Sunitinib is a standard treatment for metastatic renal cell carcinoma (RCC). Currently, the data available on the effects of sunitinib on endothelial dysfunction, metabolic changes, and cardiovascular (CV) risk factors are limited, and we aimed to evaluate these aspects in patients with RCC after a short period of treatment. METHODS: Patients affected by metastatic RCC were enrolled and evaluated before starting sunitinib (T0) and after 40 days of treatment (T1) by the flow-mediated dilation (FMD), carotid intima media thickness (IMT), ankle-brachial pressure index (ABI), and 24-hour proteinuria. We also assessed serum metabolic and nutritional parameters at T0 and T1. RESULTS: Twenty patients (7 female), with a mean age of 61.4 ± 12.0 years, were studied. Overtime, we observed a reduction in estimated glomerular filtration rate (P = .002), FMD (P = .001) and in fasting plasma glucose levels (P = .04), as well as an increase in plasma insulin (P < .001), HOMA-IR (P < .01), and serum total cholesterol levels (P = .01). Moreover at T1 we found a significant increase in systolic and diastolic blood pressure (P ≤ .001) and 24-hour proteinuria (P < .001) compared to baseline, whereas no changes in IMT and ABI were detected. CONCLUSION: The changes observed overtime after sunitinib treatment in terms of markers of early endothelial dysfunction, blood pressure, as well as in glucose/insulin metabolism and proteinuria may contribute to increase CV risk in RCC patients and suggest a strict follow-up in this setting. Larger evidences are mandatory to confirm our observations.
No takes yet. Share an insight, caveat, or question.
Lai et al. (2020) conducted an observational in Metastatic renal cell carcinoma (RCC) (n=20). Sunitinib vs. Baseline (pre-treatment) was evaluated on Flow-mediated dilation (FMD) (%) (p=0.001). Sunitinib exposure for 40 days in patients with metastatic renal cell carcinoma significantly reduced median flow-mediated dilation from 12.5% to 9.0% (P=0.001), indicating early endothelial dysfunction.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: