Evidence map›Paper›PMID 41417071›Full record

ArticleCancer immunology, immunotherapy : CII2025

Immunomodulatory effects of lenvatinib in patients with advanced thyroid cancer.

Prashant Changoer, Chunying Peng, Pepijn van Houten, Liesbeth van Emst, Janneke E W Walraven, Petronella B Ottevanger, Martin Jaeger, Romana T Netea-Maier

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Prashant ChangoerDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID http://orcid.org/0009-0004-5892-8706
Chunying PengDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID http://orcid.org/0000-0001-6726-6581
Pepijn van HoutenDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID http://orcid.org/0000-0002-8503-4140
Liesbeth van EmstDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, Nijmegen, the Netherlands.
Janneke E W WalravenDepartment of Medical Oncology, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID http://orcid.org/0000-0001-7161-5369
Petronella B OttevangerDepartment of Medical Oncology, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID http://orcid.org/0000-0001-8209-487X
Martin JaegerDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID http://orcid.org/0000-0001-6994-493X
Romana T Netea-MaierDepartment of Internal Medicine, Division of Endocrinology, Radboud University Medical Center, Nijmegen, the Netherlands. romana.netea-maier@radboudumc.nl.ORCID http://orcid.org/0000-0002-9603-0460

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTyrosine kinase inhibitors, including lenvatinib approved for advanced non-medullary thyroid cancer (TC), affect the immune system. As tumor-related inflammation contributes to TC pathogenesis, this study assesses the immunomodulatory effects of lenvatinib, focusing on myeloid cells.

methodsPeripheral blood was collected from 16 lenvatinib-treated and 15 untreated TC patients (cross-sectional cohort), and from eight patients before and after > 1 month of lenvatinib (longitudinal cohort). Immune profiling included cell subset counts, proteomic analyses, and ex vivo cytokine assays in peripheral blood mononuclear cells (PBMCs) and monocytes. Monocytes from healthy donors were used to evaluate metabolic activity, reactive oxygen species (ROS) production, and phagocytosis. Tumor-intrinsic effects of lenvatinib were studied by proteomics and immunophenotyping of the TPC-1 cell line.

resultsLenvatinib increased lymphocytes and reduced neutrophils. In both cohorts, lenvatinib modulated the inflammatory proteome with elevated VEGFA, CCL11, MMP-10, and TRAIL. Monocytes exposed ex vivo to lenvatinib showed reduced production of IL-1β, IL-6, IL-8, and IL-10. In patients treated with lenvatinib, monocytes displayed increased IL-1Ra and TNF, while PBMCs exhibited enhanced IFN-γ production. Monocytes from healthy donors displayed reduced glycolysis and increased ROS after lenvatinib exposure. In TPC-1 cells, lenvatinib altered the secretome and upregulated MHC class I, PD-L1, and CD40.

conclusionsLenvatinib treatment has broad immunomodulatory effects in patients with TC, including shifts in immune cell populations, changes in the proteome, and reprogramming of cytokine responses. Lenvatinib also impacts monocyte metabolism and tumor cell phenotype. These findings provide insight into the multifaceted immunological activities of lenvatinib and highlight opportunities for treatment strategies.

trial registrationNot applicable, this is a noninterventional trial.

Indexed as

Antineoplastic AgentsPhenylurea CompoundsProtein Kinase InhibitorsQuinolinesThyroid NeoplasmsAdultAgedCross-Sectional StudiesCytokinesFemaleHumansLeukocytes, MononuclearMaleMiddle AgedMonocytesAntineoplastic AgentsCytokineslenvatinibPhenylurea CompoundsProtein Kinase InhibitorsQuinolinesCirculatory biomarkersImmunomodulationLenvatinibMacrophagesMonocytesNon-medullary thyroid carcinoma

Identifiers

PMID41417071
PMCPMC12717327

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.