Evidence map›Paper›PMID 36418844›Full record

ArticleHepatology international2023

The clinical implications and molecular features of intrahepatic cholangiocarcinoma with perineural invasion.

Xian-Long Meng, Jia-Cheng Lu, Hai-Ying Zeng, Zhen Chen, Xiao-Jun Guo, Chao Gao, Yan-Zi Pei, Shu-Yang Hu, Mu Ye, Qi-Man Sun and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Hepatology international, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

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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

22 authors at 4 institutions in 2 countries.

Xian-Long Meng *Department of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Jia-Cheng Lu *Department of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Hai-Ying Zeng *Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Zhen Chen *Clinical Research Unit, Institute of Clinical Science, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Xiao-Jun GuoDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Chao GaoDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Yan-Zi PeiDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Shu-Yang HuDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Mu YeDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Qi-Man SunDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Guo-Huang YangDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Jia-Bin CaiDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Pei-Xin HuangLiver Cancer Institute, Fudan University, Shanghai, 200032, China.
Lei YvClinical Research Unit, Institute of Clinical Science, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Lv ZhangClinical Research Unit, Institute of Clinical Science, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Ying-Hong ShiDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Ai-Wu KeLiver Cancer Institute, Fudan University, Shanghai, 200032, China.
Jian ZhouDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Jia FanDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Yi ChenLiver Cancer Institute, Fudan University, Shanghai, 200032, China. chen.yi1@zs-hospital.sh.cn.
Xiao-Yong HuangDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China. huang.xiaoyong@zs-hospital.sh.cn.
Guo-Ming ShiDepartment of Liver Surgery and Transplantation, Zhongshan Hospital, Fudan University, Shanghai, 200032, China. shi.guoming@zs-hospital.sh.cn.ORCID http://orcid.org/0000-0003-3817-9117
Sun Yat-sen University · CNMinistry of Education of the People's Republic of China · CNFudan University Shanghai Cancer Center · CNFudan University · CN

Funding

Beijing Mutual Care Public Welfare Foundation GDXZ-08-05Innovative Research Group Project of the National Natural Science Foundation of China 81972232Key Technologies Research and Development Program 2019YFC1316000National College Students Innovation and Entrepreneurship Training Program 202210246001SSanming Project of Medicine in Shenzhen No. SZSM202003009the Clinical Research Plan of SHDC SHDC‑2020CR1003Athe Key Disease Joint Research Program of Xuhui District XHLHGG202103the Shanghai Municipal Natural Science Foundation 20JC1419103
6 · The paper itself

Abstract

backgroundPerineural invasion (PNI) is associated with metastasis in malignancies, including intrahepatic cholangiocarcinoma (ICC), and is correlated with poor prognosis.

methodsThe study included three large cohorts: ZS-ICC and TMA cohorts from our team, MSK cohort from a public database, and a small cohort named cohort 4. Prognostic implications of PNI were investigated in MSK cohort and TMA cohort. PNI-related genomic and transcriptomic profiles were analyzed in MSK and ZS-ICC cohorts. GO, KEGG, and ssGSEA analyses were performed. Immunohistochemistry was used to investigate the relationship between PNI and markers of neurons, hydrolases, and immune cells. The efficacy of adjuvant therapy in ICC patients with PNI was also assessed.

resultsA total of 30.6% and 20.7% ICC patients had PNI in MSK and TMA cohorts respectively. Patients with PNI presented with malignant phenotypes such as high CA19-9, the large bile duct type, lymph node invasion, and shortened overall survival (OS) and relapse-free survival (RFS). Nerves involved in PNI positively express tyrosine hydroxylase (TH), a marker of sympathetic nerves. Patients with PNI showed high mutation frequency of KRAS and an immune suppressive metastasis prone niche of decreased NK cell, increased neutrophil, and elevated PD-L1, CD80, and CD86 expression. Patients with PNI had an extended OS after adjuvant therapy with TEGIO, GEMOX, or capecitabine.

conclusionOur study deciphered the genomic features and the immune suppressive metastasis-prone niche in ICC with PNI. Patients with PNI showed a poor prognosis after surgery but a good response to adjuvant chemotherapy.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaBile Ducts, IntrahepaticHumansNeoplasm InvasivenessNeoplasm Recurrence, LocalPrognosisRetrospective StudiesAdjuvant therapyBioinformaticsIntrahepatic cholangiocarcinomaKRASMetastasis prone nicheOverall survivalPathology featurePerineural invasionRelapse-free survivalSympathetic nerve

Identifiers

PMID36418844
PMCPMC9895046
OpenAlexW4309927438

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Registered trials

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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.