Evidence map›Paper›PMID 32229792›Full record

ArticleCancer research and treatment2020

Prognostic Value of TP53 Mutation for Transcatheter Arterial Chemoembolization Failure/Refractoriness in HBV-Related Advanced Hepatocellular Carcinoma.

Miao Xue, Yanqin Wu, Wenzhe Fan, Jian Guo, Jialiang Wei, Hongyu Wang, Jizhou Tan, Yu Wang, Wang Yao, Yue Zhao and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Cancer research and treatment, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
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

16 citing papers in PubMed, 19 citations in OpenAlex.

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  9. New insights into mechanisms and interventions of locoregional therapies for hepatocellular carcinoma.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2024
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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

11 authors at 2 institutions in 1 country.

Miao XueDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Yanqin WuDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Wenzhe FanDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Jian GuoDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Jialiang WeiDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Hongyu WangDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Jizhou TanDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Yu WangDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Wang YaoDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Yue ZhaoDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Jiaping LiDepartment of Interventional Oncology, the First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Sun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

Major program for tackling key problems of Guangzhou City, China 201704020144National Natural Science Foundation of China 81671797Science and Technology Planning Project of Guangdong Province 2017B030308006
6 · The paper itself

Abstract

purposeThis study aimed to investigate the clinicopathologic features and mutational landscape of patients with hepatitis B virus (HBV)-related advanced hepatocellular carcinomas (HCC) undergoing transcatheter arterial chemoembolization (TACE). MATERIALS AND

methodsFrom January 2017 to December 2018, 38 patients newly diagnosed with HBV-related advanced HCC were enrolled in the final analysis. Their pathological tissues and corresponding blood samples before TACE treatment were collected for whole-exome sequencing. Response to TACE was evaluated at 1-3 months after two consecutive use of TACE. Predictive factors were analyzed by univariate and multivariate analyses in a bivariate Logistic regression model. Enrichment of related pathways of all driver genes were acquired using the gene set enrichment analysis (GSEA).

resultsAmong 38 patients, 23 (60.5%) exhibited TACE failure/refractoriness. Patients with TACE failure/refractoriness showed higher frequency of TP53 mutation than their counterparts (p=0.020). Univariate and multivariate analyses showed that only vascular invasion and TP53 mutation were significantly correlated with TACE failure/refractoriness in HBV-related advanced HCC. Of the 16 patients without vascular invasion, eight (50.0%) had TP53 mutations, and TP53 mutation was associated with TACE failure/refractoriness (p=0.041). Moreover, GSEA showed that mitogen-activated protein kinase and apoptosis pathways induced by TP53 mutation were possibly associated with TACE failure/refractoriness.

conclusionOur study suggested that TP53 mutation was independently related with TACE efficacy, which may work via mitogen-activated protein kinase and apoptosis pathways. These findings may provide evidence to help distinguish patients who will particularly benefit from TACE from those who require more personalized therapeutic regimens and rigorous surveillance in HBV-related advanced HCC.

Indexed as

MutationCarcinoma, HepatocellularChemoembolization, TherapeuticChinaDrug Resistance, NeoplasmFemaleFollow-Up StudiesHepatitis BHepatitis B virusHumansLiver NeoplasmsMaleMiddle AgedNeoplasm Recurrence, LocalPrognosisRetrospective StudiesTP53 protein, humanTumor Suppressor Protein p53Hepatocellular carcinomaTranscatheter arterial chemoembolizationTreatment outcomeTumor protein p53Tumor responseWhole-exome sequencing

Identifiers

PMID32229792
PMCPMC7373860
OpenAlexW3013802397

What OpenQuestion holds

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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.