Saito Kei, Fujii Hideki, Kono Keiji, Hirabayashi Ken, Yamatani Satoshi, Watanabe Kentaro, Goto Shunsuke, Komatsu Shohei, Fukumoto Takumi, Nishi Shinichi
Division of Nephrology and Kidney Center, Kobe University Graduate School of Medicine, Kobe, Japan.
Department of Surgery, Division of Hepato-Biliary-Pancreatic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.
Clin Kidney J. 2020 Oct 21;14(1):325-331. doi: 10.1093/ckj/sfaa137. eCollection 2021 Jan.
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.
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.
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.
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.
在用于治疗多种晚期癌症的酪氨酸激酶抑制剂(TKIs)类别中,与其他TKIs相比,乐伐替尼与高血压(HT)的更高患病率相关。在本研究中,我们调查了乐伐替尼对血压(BP)的影响及相关因素。
这项单中心回顾性观察研究纳入了2018年4月至2018年12月在研究机构接受乐伐替尼治疗不可切除肝细胞癌的25例连续患者。我们使用动态血压监测、尿钠排泄、肾功能、抗高血压药物和利尿剂的使用以及乐伐替尼治疗开始后的液体潴留情况评估血压变化。
治疗开始后1周,平均血压和血压升高模式患者的百分比与基线相比显著增加。虽然1周时无显著变化,但尿钠排泄(第1周和第3周分别为153.4±51.7和112.5±65.0 mEq/天,P<0.05)和估计肾小球滤过率显著降低,第3周液体潴留患者数量增加。此外,与无液体潴留的患者相比,有液体潴留的患者血压显著更高或需要更强化的血压治疗。
乐伐替尼在治疗开始后不久可能导致无液体潴留的高血压,随后导致尿钠排泄减少,从而通过液体潴留导致血压升高。