Evidence map›Paper›PMID 41559002›Full record

ArticleCancer reports (Hoboken, N.J.)2026

Clinical Course and Risk Factors of Lenvatinib-Related Hypothyroidism in Hepatocellular Carcinoma: A Retrospective Cohort Study.

Chihiro Shiraishi, Hideo Kato, Yuki Asai, Takuya Iwamoto

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Chihiro ShiraishiDepartment of Pharmaceutical Sciences for Health Crisis Management, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.ORCID 0000-0002-1190-6540
Hideo KatoDepartment of Pharmacy, Mie University Hospital, Mie, Japan.ORCID 0000-0002-5272-9560
Yuki AsaiDepartment of Pharmacy, Mie University Hospital, Mie, Japan.ORCID 0000-0002-1933-8592
Takuya IwamotoDepartment of Pharmacy, Mie University Hospital, Mie, Japan.ORCID 0000-0002-6445-4410

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLenvatinib-related hypothyroidism occurs in 16%-22% of patients with hepatocellular carcinoma and may affect treatment management. Previous studies have reported elevated serum thyroid stimulating hormone (TSH) levels despite levothyroxine therapy, indicating the need for research on the optimal levothyroxine dose during lenvatinib therapy.

aimsWe aimed to explore the effect of lenvatinib on thyroid function, focusing on lenvatinib pharmacokinetics and factors influencing hypothyroidism development. METHODS AND

resultsA retrospective cohort study involving 56 patients with hepatocellular carcinoma treated with lenvatinib was conducted at the Mie University Hospital. The primary outcome was grade ≥ 2 hypothyroidism. Demographic data, treatment details, and clinical outcomes were analyzed to identify factors associated with lenvatinib-related hypothyroidism. In addition, we assessed the levothyroxine dose administered during treatment and the dose required to achieve TSH levels < 10 mIU/L. Twelve patients (21%) developed hypothyroidism during lenvatinib therapy. The median levothyroxine dose and time to onset of hypothyroidism were 25.0 [25.0-50.0] μg/day and 81.0 [15.0-208.0] days, respectively. Levothyroxine therapy was initiated at either a low or recommended dose, with 10 patients achieving TSH levels < 10 mIU/L. Significant predictors of hypothyroidism included age ≤ 63 years and a higher daily lenvatinib dose (≥ 0.152 mg/kg/day).

conclusionInitiation of levothyroxine therapy, even at lower doses, may be effective in managing lenvatinib-related hypothyroidism. Underweight patients (e.g., body weight < 50 kg) require particular attention due to their increased susceptibility to hypothyroidism. Even though this study has limitations such as a small sample size and the lack of multivariate analysis, it provides valuable information for managing lenvatinib-related hypothyroidism.

Indexed as

Antineoplastic AgentsCarcinoma, HepatocellularHypothyroidismLiver NeoplasmsPhenylurea CompoundsProtein Kinase InhibitorsQuinolinesAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsThyrotropinAntineoplastic AgentslenvatinibPhenylurea CompoundsProtein Kinase InhibitorsQuinolinesThyrotropinThyroxinelenvatinib‐related hypothyroidismthyroid dysfunctiontyrosine kinase inhibitor

Identifiers

PMID41559002
PMCPMC12819047

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.