Evidence map›Paper›PMID 31474758›Full record

ArticleBritish journal of cancer2019

CK7 and consensus molecular subtypes as major prognosticators in

Fotios Loupakis, Paola Biason, Alessandra Anna Prete, Chiara Cremolini, Filippo Pietrantonio, Nicoletta Pella, Emanuela Dell'Aquila, Elisa Sperti, Clizia Zichi, Rossana Intini and 22 more

Abstract read
In one paragraph

Article in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
–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

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
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  8. Article
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  14. Cancers · 2020
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  19. Clinicopathologic Features and Prognosis ofFrontiers in oncology · 2020
    Article
  20. Article
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

32 authors.

Fotios LoupakisDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy. fotios.loupakis@iov.veneto.it.
Paola BiasonDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Alessandra Anna PreteDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Chiara CremoliniDepartment of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Filippo PietrantonioDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Nicoletta PellaDepartment of Oncology, University and General Hospital, Udine, Italy.
Emanuela Dell'AquilaDepartment of Medical Oncology, Campus Bio-Medico University of Rome, Rome, Italy.
Elisa SpertiDepartment of Oncology, University of Turin at Umberto I "Ordine Mauriziano" Hospital, Turin, Italy.
Clizia ZichiDepartment of Oncology, University of Turin at Umberto I "Ordine Mauriziano" Hospital, Turin, Italy.
Rossana IntiniDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Vincenzo DadduzioDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Marta SchirripaDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Francesca BergamoDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Carlotta AntoniottiDepartment of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Federica MoranoDepartment of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Francesco CortiulaDepartment of Oncology, University and General Hospital, Udine, Italy.
Giovanna De MaglioDepartment of Pathology, University Hospital of Udine, Udine, Italy.
Lorenza RimassaMedical Oncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center-IRCCS Rozzano, Milan, Italy.
Valeria SmiroldoMedical Oncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center-IRCCS Rozzano, Milan, Italy.
Lorenzo CalvettiDepartment of Oncology, General Hospital San Bortolo, Unità Locale Socio-Sanitaria 8 Berica, Vicenza, Italy.
Giuseppe AprileDepartment of Oncology, General Hospital San Bortolo, Unità Locale Socio-Sanitaria 8 Berica, Vicenza, Italy.
Lisa SalvatoreUnit of Oncology, Polyclinic GB Rossi, AOUI, Verona, Italy.
Daniele SantiniDepartment of Medical Oncology, Campus Bio-Medico University of Rome, Rome, Italy.
Giada MunariDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Roberta SalmasoSurgical Pathology & Cytopathology Unit, Department of Medicine (DIMED), University of Padua, Padua, Italy.
Vincenza GuzzardoSurgical Pathology & Cytopathology Unit, Department of Medicine (DIMED), University of Padua, Padua, Italy.
Claudia MescoliSurgical Pathology & Cytopathology Unit, Department of Medicine (DIMED), University of Padua, Padua, Italy.
Sara LonardiDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Massimo RuggeSurgical Pathology & Cytopathology Unit, Department of Medicine (DIMED), University of Padua, Padua, Italy.
Vittorina ZagonelDepartment of Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Massimo Di MaioDepartment of Oncology, University of Turin at Umberto I "Ordine Mauriziano" Hospital, Turin, Italy.
Matteo FassanSurgical Pathology & Cytopathology Unit, Department of Medicine (DIMED), University of Padua, Padua, Italy. matteo.fassan@unipd.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background

methodsData and tissue specimens from 155

resultsCDX2 loss conferred worse OS (HR = 1.72, 95%CI 1.03-2.86, p = 0.036), as well as high CK7 expression (HR = 2.17, 95%CI 1.10-4.29, p = 0.026). According to Consensus Molecular Subtypes (CMS), CMS1 patients had better OS compared to CMS2-3/CMS4 (HR = 0.37, 95%CI 0.19-0.71, p = 0.003). Samples showing less TILs had worse OS (HR = 1.72, 95%CI 1.16-2.56, p = 0.007). Progression-free survival analyses led to similar results. At multivariate analysis, CK7 and CMS subgrouping retained their significant correlation with OS.

conclusionThe present study provides new evidence on how several well-established biomarkers perform in a homogenous

Indexed as

MutationAdultAgedAged, 80 and overAnalysis of VarianceBiomarkers, TumorCDX2 Transcription FactorColorectal NeoplasmsCytoskeletal ProteinsFemaleGene DeletionGenes, MCCHumansKeratin-20Keratin-7Lymphocytes, Tumor-InfiltratingBiomarkers, TumorCDX2 protein, humanCDX2 Transcription FactorCytoskeletal ProteinsKeratin-20Keratin-7KRT20 protein, humanKRT7 protein, humanMSH2 protein, humanMutS Homolog 2 ProteinProto-Oncogene Proteins B-raf

Identifiers

PMID31474758
PMCPMC6889398

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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.