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Risk factors for lenvatinib-induced hypertension in patients with hepatocellular carcinoma: a retrospective study
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  • Shusuke Uekusa,
  • Misaki Nakashin,
  • Yuki Hanai,
  • Maho Nemoto,
  • Sachiko Yanagino,
  • Yoshiki Arita,
  • Takahiro Matsumoto,
  • Noritaka Wakui,
  • Hidenari Nagai,
  • Koji Higai,
  • Kazuhiro Matsuo
Shusuke Uekusa
Faculty of Pharmaceutical Sciences, Toho University

Corresponding Author:[email protected]

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Misaki Nakashin
Faculty of Pharmaceutical Sciences, Toho University
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Yuki Hanai
Toho University
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Maho Nemoto
Faculty of Pharmaceutical Sciences, Toho University
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Sachiko Yanagino
Toho University Omori Medical Center
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Yoshiki Arita
Toho University Omori Medical Center
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Takahiro Matsumoto
Toho University Omori Medical Center
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Noritaka Wakui
Toho University
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Hidenari Nagai
Toho University
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Koji Higai
Toho University
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Kazuhiro Matsuo
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Abstract

Aims: Lenvatinib mesylate (LEN) is an orally administered tyrosine kinase inhibitor (TKI) used to treat various cancers, including hepatocellular carcinoma (HCC). LEN therapy for HCC is associated with a high incidence of adverse events, including hypertension (HTN). However, the risk factors associated with LEN therapy remain unclear. This study aimed to investigate the incidence of LEN-induced HTN (LENiHTN) and the relationship between the incidence of HTN and patient demographics in patients with HCC receiving LEN therapy. Methods: This was a single-centre, retrospective study of patients with HCC who received LEN therapy between 19 April 2018 and 30 September 2020. The observation period was from 1 week before the start to 1 month after the end of LEN administration. Results: In total, 75 patients with HCC were enrolled. LENiHTN of any grade was found in 74.7% of patients. The use of two or more antihypertensive agents before starting LEN was more common (P = 0.007); serum potassium (K), and albumin–bilirubin score (ALBI) were lower (P = 0.013 and 0.038, respectively); and albumin (Alb) was higher (P = 0.025). The cut-off values of K, Alb, and ALBI for HTN were estimated to be 4.1 mEq L-1, 3.1 g dL-1, and -1.736, respectively. In the multivariate analysis, K and ALBI were independent risk factors for LENiHTN. Conclusion: Low K and high ALBI were independent risk factors for LENiHTN. Systematic evaluation of HTN risk and early intervention for HTN prevention among high-risk patients can markedly enhance the efficacy and utilisation of LEN therapy.
01 Apr 2024Submitted to British Journal of Clinical Pharmacology
01 Apr 2024Submission Checks Completed
01 Apr 2024Assigned to Editor
01 Apr 2024Review(s) Completed, Editorial Evaluation Pending
10 Apr 2024Reviewer(s) Assigned
27 Jul 2024Editorial Decision: Revise Major
11 Oct 20241st Revision Received
14 Oct 2024Submission Checks Completed
14 Oct 2024Assigned to Editor
14 Oct 2024Review(s) Completed, Editorial Evaluation Pending
20 Oct 2024Editorial Decision: Accept