Association between baseline blood pressure and the incidence of lenvatinib‐induced hypertension in patients with thyroid cancer

Author:

Shibutani Yuma12ORCID,Tajiri Kazuko34ORCID,Suzuki Shinya1ORCID,Enokida Tomohiro5ORCID,Sagara Atsunobu2,Okano Susumu5,Fujisawa Takao5,Sato Fumiaki2,Yumoto Tetsuro2,Sano Motohiko2,Kawasaki Toshikatsu1ORCID,Tahara Makoto5

Affiliation:

1. Department of Pharmacy National Cancer Center Hospital East Kashiwa Japan

2. Hoshi University School of Pharmacy and Pharmaceutical Sciences Shinagawa Japan

3. Department of Cardiology National Cancer Center Hospital East Kashiwa Japan

4. Tsukuba Life Science Innovation Program (T‐LSI), School of Integrative and Global Majors (SIGMA) University of Tsukuba Tsukuba Japan

5. Department of Head and Neck Medical Oncology National Cancer Center Hospital East Kashiwa Japan

Abstract

AbstractBackgroundHypertension is the most frequently occurring adverse event of lenvatinib, recognized relatively early in its course. However, the trend in blood pressure after the initiation of lenvatinib and the outcomes with antihypertensive treatment are unclear. This study aimed to clarify the association between baseline blood pressure and the incidence of lenvatinib‐induced hypertension in patients with thyroid cancer.MethodsThis retrospective study included 65 patients without hypertension at the time of lenvatinib initiation. Patients were divided into two groups: those who developed hypertension grade ≥3 (HTN group) and those who did not develop hypertension grade ≥3 (non‐HTN group).ResultsOf the 65 patients, 46 (71%) developed hypertension grade ≥3. In both HTN and non‐HTN groups, blood pressure significantly increased the day after lenvatinib initiation. There was no significant difference in the elevated values of both the changes in systolic blood pressure (ΔSBP) and diastolic blood pressure (ΔDBP) between the two groups, with an average increase of 20 mmHg in SBP and 13 mmHg in DBP from baseline. The median (range) time to the onset of hypertension grade ≥3 was 2 days (1–12 days). In the multivariable analysis, patients with normal (SBP 120–129 mmHg and/or DBP 80–84 mmHg) or high‐normal baseline blood pressure (SBP 130–139 mmHg and/or DBP 85–89 mmHg) were at higher risk of developing hypertension grade ≥3 than those with optimal baseline blood pressure (SBP <120 mmHg and DBP <80 mmHg) (odds ratio [OR], 5.07; 95% confidential interval [CI] 1.09–23.54 and OR, 7.48; 95% CI, 1.67–33.51, respectively).ConclusionsLenvatinib‐induced hypertension appears the day after administration, and higher baseline blood pressure is a significant risk factor for developing hypertension grade ≥3. In cases of increased blood pressure with lenvatinib, early initiation of antihypertensives may prevent treatment interruption due to hypertension and maintain the therapeutic intensity of lenvatinib.

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

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