Key result
Lenvatinib treatment significantly decreased urinary sodium excretion from 153.4 mEq/day at 1 week to 112.5 mEq/day at 3 weeks (P<0.05), contributing to fluid retention and increased blood pressure.
Why the study?
Among tyrosine kinase inhibitors used for advanced cancers, lenvatinib is associated with a higher prevalence of hypertension, prompting investigation into its effect on blood pressure and associated factors.
Does lenvatinib increase blood pressure and affect fluid retention in patients with unresectable hepatocellular carcinoma?
Observational (n=25)
No
Does lenvatinib increase blood pressure and affect fluid retention in patients with unresectable hepatocellular carcinoma?
Absolute Event Rate: 112.5% vs 153.4%
p-value: p=<0.05
Lenvatinib treatment leads to an early rise in blood pressure, followed by reduced urinary sodium excretion and fluid retention, which may further exacerbate hypertension.
May worsen hypertension via sodium retention in HCC; leaves open prospective trials on fluid management.
BACKGROUND: Within the class of tyrosine kinase inhibitors (TKIs), which are used for the treatment of numerous advanced cancers, lenvatinib is associated with a higher prevalence of hypertension (HT) compared with other TKIs. In this study, we investigated the effect of lenvatinib on blood pressure (BP) and associated factors. METHODS: This single-centre, retrospective observational study included 25 consecutive patients treated with lenvatinib for unresectable hepatocellular carcinoma from April 2018 to December 2018 at the study institution. We assessed changes in BP using ambulatory BP monitoring, urinary sodium excretion, kidney function, use of antihypertensive agents and diuretics, and fluid retention following treatment initiation with lenvatinib. RESULTS: At 1 week after treatment initiation, the mean BP and the percentage of patients with riser pattern significantly increased compared with those at the baseline. Although there were no significant changes at 1 week, urinary sodium excretion (153.4 ± 51.7 and 112.5 ± 65.0 mEq/day at 1 and 3 weeks, respectively, P < 0.05) and estimated glomerular filtration rate significantly decreased and the number of patients with fluid retention increased at 3 weeks. Furthermore, patients with fluid retention had significantly higher BP or required more intensive BP treatment compared with those without fluid retention. CONCLUSIONS: Lenvatinib might lead to HT without fluid retention soon after the initiation of treatment, subsequently leading to a reduction in urinary sodium excretion, thereby contributing to a rise in BP by fluid retention.
No takes yet. Share an insight, caveat, or question.
Saito et al. (2020) conducted an observational in unresectable hepatocellular carcinoma (n=25). Lenvatinib vs. Baseline / 1 week post-initiation was evaluated on Urinary sodium excretion (p=<0.05). Lenvatinib treatment significantly decreased urinary sodium excretion from 153.4 mEq/day at 1 week to 112.5 mEq/day at 3 weeks (P<0.05), contributing to fluid retention and increased blood pressure.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: