Evidence map›Paper›PMID 39047713›Full record

ArticleOncology2024

Changes in Mutations of Cell-Free DNA and Liver Tumor Tissue in Patients with Advanced Hepatocellular Carcinoma before and after Introduction of Lenvatinib.

Mio Tsuruoka, Masashi Ninomiya, Jun Inoue, Tomoaki Iwata, Akitoshi Sano, Kosuke Sato, Masazumi Onuki, Satoko Sawahashi, Atsushi Masamune

Abstract read
In one paragraph

Article in Oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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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

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Mio TsuruokaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan, ytrsb237@gmail.com.
Masashi NinomiyaDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Jun InoueDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tomoaki IwataDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Akitoshi SanoDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Kosuke SatoDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Masazumi OnukiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Satoko SawahashiDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Atsushi MasamuneDivision of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCell-free DNA (cfDNA) is expected to contribute to the decision for treatment and prediction of effects with minimally invasion. We investigated the correlation between gene mutations before and after lenvatinib (LEN) treatment and its effectiveness, in order to find advanced hepatocellular carcinoma (HCC) patients who would benefit greatly from the therapy.

methodsWe analyzed cfDNA before and 6-8 weeks after the start of treatment in 20 advanced HCC patients who started LEN. A next-generation sequencer was used for CTNNB1 and TP53. Concerning TERT promoter, -124C>T and -146C>T mutations are researched using digital PCR. In addition, we examined liver tumor biopsy tissues by the same method. Computerized tomography evaluation was performed at 6-8 weeks and 3-4 months to assess the efficacy.

resultsFrequencies of TERT promoter, CTNNB1, and TP53 mutations in pretreatment cfDNA were 45%, 65%, and 65%, but 53%, 41%, and 47% in HCC tissues, respectively. There were no clear correlations between these gene mutations and the disease-suppressing effect or progression-free survival. Overall, there were many cases showing a decrease in mutations after LEN treatment. Integrating the reduction of CTNNB1 and TP53 genetic mutations increased the potential for disease suppression.

conclusionThis study suggests that analysis of cfDNA in advanced HCC patients may be useful for identifying LEN responders and determining therapeutic efficacy. Furthermore, it has potential for selecting responders for other molecular-targeted drugs.

Indexed as

beta CateninCarcinoma, HepatocellularCell-Free Nucleic AcidsLiver NeoplasmsMutationPhenylurea CompoundsQuinolinesTelomeraseAdultAgedAged, 80 and overAntineoplastic AgentsFemaleHumansMaleMiddle AgedAntineoplastic Agentsbeta CateninCell-Free Nucleic AcidsCTNNB1 protein, humanlenvatinibPhenylurea CompoundsQuinolinesTelomeraseTERT protein, humanTP53 protein, humanTumor Suppressor Protein p53Cell-free DNACTNNB1Hepatocellular carcinomaLenvatinibLiver tumor biopsyNext-generation sequencerTelomerase reverse transcriptase promoterTP53

Identifiers

PMID39047713
PMCPMC11614310

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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.