Evidence map›Paper›PMID 38767772›Full record

ArticleHepatology international2024

Tertiary lymphoid structures as a potential prognostic biomarker for combined hepatocellular-cholangiocarcinoma.

Wenchen Gong, Su Zhang, Xiangdong Tian, Wenshuai Chen, Yuchao He, Liwei Chen, Tingting Ding, Peiqi Ren, Lin Shi, Qiang Wu and 3 more

Abstract read
In one paragraph

Article in Hepatology international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

13 authors.

Wenchen Gong *Department of Pathology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.
Su Zhang *Department of Gynecological Oncology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.
Xiangdong Tian *Department of Endoscopic Diagnosis and Therapy, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.
Wenshuai ChenDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.
Yuchao HeDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.
Liwei ChenDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.
Tingting DingDepartment of Pathology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.
Peiqi RenDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.
Lin ShiDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China.
Qiang WuDepartment of Hepatobiliary Cancer, Tianjin Medical University Cancer Institute and Hospital, Liver Cancer Research Center, Tianjin, 300060, China. wuqiangtianjin@hotmail.com.
Yan SunDepartment of Pathology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China. sunyan@tjmuch.com.
Lu ChenDepartment of Hepatobiliary Cancer, Tianjin Medical University Cancer Institute and Hospital, Liver Cancer Research Center, Tianjin, 300060, China. chenlu@tmu.edu.cn.
Hua GuoDepartment of Tumor Cell Biology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, 300060, China. guohua@tjmuch.com.ORCID http://orcid.org/0000-0002-3345-8005

Funding

National Natural Science Foundation of China 82173208National Natural Science Foundation of China 82203423National Natural Science Foundation of China 82373365Natural Science Foundation of Tianjin Municipality 23JCYBJC00600Tianjin Health Science and Technology Project TJWJ2022MS008Tianjin Key Medical Discipline (Pathology) Construction Project TJYXZDXK-012A
6 · The paper itself

Abstract

backgroundCombined hepatocellular-cholangiocarcinoma (cHCC-CCA), as a rare primary hepatic tumor, is challenging to accurately assess in terms of the clinical outcomes and prognostic risk factors in patients. This study aimed to clarify the function of tertiary lymphoid structure (TLS) status in predicting the outcome of cHCC-CCA and to preliminarily explore the possible mechanism of TLS formation.

methodsThe TLSs, with different spatial distributions and densities, of 137 cHCC-CCA were quantified, and their association with prognosis was assessed by Cox regression and Kaplan-Meier analyses. We further validated TLS possible efficacy in predicting immunotherapy responsiveness in two cHCC-CCA case reports. TLS composition and its relationship to CXCL12 expression were analysed by fluorescent multiplex immunohistochemistry.

resultsA high intratumoural TLS score was correlated with prolonged survival, whereas a high TLS density in adjacent tissue indicated a worse prognosis in cHCC-CCA. Mature TLSs were related to favorable outcomes and showed more CD8 + T cells infiltrating tumor tissues. We further divided the cHCC-CCA patients into four immune grades by combining the peri-TLS and intra-TLS, and these grades were an independent prognostic factor. In addition, our reported cases suggested a potential value of TLS in predicting immunotherapy response in cHCC-CCA patients. Our findings suggested that CXCL12 expression in cHCC-CCA tissue was significantly correlated with TLS presence.

conclusionThe spatial distribution and density of TLSs revealing the characteristics of the cHCC-CCA immune microenvironment, significantly correlated with prognosis and provided a potential immunotherapy response biomarker for cHCC-CCA.

Indexed as

Bile Duct NeoplasmsCarcinoma, HepatocellularCholangiocarcinomaLiver NeoplasmsTertiary Lymphoid StructuresAgedBiomarkers, TumorChemokine CXCL12FemaleHumansImmunotherapyLymphocytes, Tumor-InfiltratingMaleMiddle AgedPrognosisTumor MicroenvironmentBiomarkers, TumorChemokine CXCL12CXCL12 protein, humanCombined hepatocellular–cholangiocarcinomaCXCL12Immunotherapy responsePrognosisTertiary lymphoid structures

Identifiers

PMID38767772
PMCPMC11297834

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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.