Evidence map›Paper›PMID 30448973›Full record

ReviewPathology oncology research : POR2020

Cholangiocarcinoma: Classification, Histopathology and Molecular Carcinogenesis.

Gábor Lendvai, Tímea Szekerczés, Idikó Illyés, Réka Dóra, Endre Kontsek, Alíz Gógl, András Kiss, Klára Werling, Ilona Kovalszky, Zsuzsa Schaff and 1 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pathology oncology research : POR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
6.6field-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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 104 citations in OpenAlex.

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11 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Gábor Lendvai2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.ORCID http://orcid.org/0000-0002-0931-380X
Tímea Szekerczés2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Idikó Illyés2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Réka Dóra2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Endre Kontsek2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Alíz Gógl2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
András Kiss2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Klára Werling2nd Department of Internal Medicine, Semmelweis University, Budapest, 1085, Hungary.
Ilona Kovalszky1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, 1085, Hungary.
Zsuzsa Schaff2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary. schaff.zsuzsa@med.semmelweis-univ.hu.
Katalin Borka2nd Department of Pathology, Semmelweis University, Üllői út 93, Budapest, H-1091, Hungary.
Semmelweis University · HU

Funding

Hungarian National Research, Development and Innovation Office NVKP_16_1-2016-0004Országos Tudományos Kutatási Alapprogramok 108548
6 · The paper itself

Abstract

Cholangiocarcinoma (CC) is the second most common tumor of the liver, originating from the biliary system with increasing incidence and mortality worldwide. Several new classifications review the significance of tumor localization, site of origin, proliferation and biomarkers in the intrahepatic, perihilar and distal forms of the lesion. Based on growth pattern mass-forming, periductal-infiltrating, intraductal, undefined and mixed types are differentiated. There are further subclassifications which are applied for the histological features, in particular for intrahepatic CC. Recognition of the precursors and early lesions of CC including biliary intraepithelial neoplasia (BilIN), intraductal papillary neoplasm of the bile ducts (IPNB), biliary mucinous cystic neoplasm (MCNB) and the candidate precursors, such as bile duct adenoma and von Meyenburg complex is of increasing significance. In addition to the previously used biliary markers detected by immunohistochemistry, several new markers have been added to the differentiation of both the benign and malignant lesions, which can be used to aid in the subclassification in association with the outcome of CC. Major aspects of biliary carcinogenesis have been revealed, yet, the exact way of this diverse process is still unclear. The factors contributing to molecular cholangiocarcinogenesis include various risk factors, different anatomical localizations, multiple cellular origins, genetic and epigenetic alterations, tumor microenvironment, heterogeneity and clonal evolution. Driver mutations have been identified, implying that they are optimal candidates for targeted therapy. The most promising therapeutic candidates have entered clinical trials.

Indexed as

Bile Duct NeoplasmsBiomarkers, TumorCarcinogenesisCholangiocarcinomaHumansLiver NeoplasmsMicroRNAsMutationNeoplasm StagingPrecancerous ConditionsPrognosisTumor MicroenvironmentBiomarkers, TumorMicroRNAsBiliary markersCholangiocarcinomaLiver cancerMicroRNAStem cells

Identifiers

PMID30448973
OpenAlexW2901213952

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.