Key result
VEGFR-TKI treatment significantly impaired left ventricular diastolic function in patients with preserved ejection fraction, reducing septal e' velocity from 6.1 to 5.0 cm/s (P < 0.01).
Why the study?
While VEGFR-TKIs are known to impair left ventricular systolic function, their effects on left ventricular diastolic function remain to be fully elucidated.
Does VEGFR-TKI monotherapy impair left ventricular diastolic function in patients with preserved LVEF?
Cohort (n=24)
No
Does VEGFR-TKI monotherapy impair left ventricular diastolic function in patients with preserved LVEF?
Absolute Event Rate: 5% vs 6.1%
p-value: p=<0.01
VEGFR-TKI therapy significantly impairs left ventricular diastolic function in patients with preserved LVEF, particularly those with pre-existing risk factors for HFpEF.
May warrant diastolic monitoring with VEGFR-TKIs; hypothesis-generating for cardiotoxicity in preserved EF.
Vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR-TKIs) frequently induce cardiovascular adverse events, though VEGFR-TKIs contribute to the improvement of the prognosis of patients with malignancies. It is widely accepted that VEGFR-TKIs impair left ventricular systolic functions; however, their effects on diastolic functions remain to be fully elucidated. The purpose of this study was to analyze the impact of VEGFR-TKIs on left ventricular diastolic functions. This study was designed as a retrospective single-center cohort study in Japan. We assessed 24 cases who received VEGFR-TKI monotherapy (sunitinib, sorafenib, pazopanib, axitinib) with left ventricular ejection fraction (LVEF) above 50% during the therapy at the Osaka University Hospital from January 2008 to June 2019. Left ventricular diastolic functions were evaluated by the change in echocardiographic parameters before and after the VEGFR-TKI treatment. Both septal e' and lateral e's decreased after treatment (septal e': before, 6.1 ± 1.8; after, 5.0 ± 1.9; n = 21, P < 0.01; lateral e': before, 8.7 ± 2.8; after, 6.9 ± 2.3; n = 21, P < 0.01). E/A declined after VEGFR-TKIs administration, though not statistically significantly. In 20 cases with at least one risk factor for heart failure with preserved ejection fraction (HFpEF), E/A significantly decreased (0.87 ± 0.34 versus 0.68 ± 0.14; P < 0.05) as well as the septal and lateral e's. These results suggest that treatment with VEGFR-TKIs impairs left ventricular diastolic functions in patients with preserved LVEF, especially in those with risk factors for HFpEF.
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Yokoyama et al. (2021) conducted a cohort in Malignancies (n=24). VEGFR-TKI monotherapy vs. Baseline (before treatment) was evaluated on Septal e' velocity (cm/second) (p=<0.01). VEGFR-TKI treatment significantly impaired left ventricular diastolic function in patients with preserved ejection fraction, reducing septal e' velocity from 6.1 to 5.0 cm/s (P < 0.01).
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