Evidence map›Paper›PMID 30511046›Full record

ArticleBJS open2018

Effects of CDX2 on prognosis and chemotherapy responsiveness in mismatch repair-deficient colorectal cancer.

É J Ryan, B Creavin, Y L Khaw, M E Kelly, H M Mohan, R Geraghty, E J Ryan, R Kennelly, A Hanly, S T Martin and 6 more

Open access · goldAbstract read
In one paragraph

Article in BJS open, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Optimizing the Personalized Care for the Management of Rectal Cancer: A Consensus Statement.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2022
    Article
  3. Article
  4. Article
  5. Mismatch repair phenotype determines the implications of tumor grade and CDX2 expression in stage II-III colon cancer.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  6. 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

16 authors at 2 institutions in 1 country.

É J RyanDepartment of Surgery, St Vincent's University Hospital Dublin Ireland.ORCID https://orcid.org/0000-0003-2609-0836
B CreavinDepartment of Surgery, St Vincent's University Hospital Dublin Ireland.ORCID https://orcid.org/0000-0001-8209-4810
Y L KhawDepartment of Histopathology, St Vincent's University Hospital Dublin Ireland.
M E KellyDepartment of Surgery, St Vincent's University Hospital Dublin Ireland.
H M MohanDepartment of Surgery, St Vincent's University Hospital Dublin Ireland.
R GeraghtyDepartment of Histopathology, St Vincent's University Hospital Dublin Ireland.
E J RyanSchool of Medicine and Medical Sciences University College Dublin Dublin Ireland.
R KennellyDepartment of Surgery, St Vincent's University Hospital Dublin Ireland.
A HanlyDepartment of Surgery, St Vincent's University Hospital Dublin Ireland.
S T MartinDepartment of Surgery, St Vincent's University Hospital Dublin Ireland.
D FennellyDepartment of Oncology, St Vincent's University Hospital Dublin Ireland.
R McDermottDepartment of Oncology, St Vincent's University Hospital Dublin Ireland.
D GibbonsDepartment of Histopathology, St Vincent's University Hospital Dublin Ireland.
P R O'ConnellDepartment of Surgery, St Vincent's University Hospital Dublin Ireland.
K SheahanDepartment of Histopathology, St Vincent's University Hospital Dublin Ireland.
D C WinterDepartment of Surgery, St Vincent's University Hospital Dublin Ireland.
University College Dublin · IESt. Vincent's University Hospital · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCaudal-related homeobox transcription factor 2 (CDX2) is an intestine-specific transcription factor implicated in tumour differentiation, proliferation, cell adhesion and migration. Negative CDX2 status (CDX2-) is associated with worse prognosis in colorectal cancer and may identify high-risk stage II disease that benefits from adjuvant chemotherapy. This observational study investigated whether CDX2- is associated with prognosis or response to chemotherapy in the mismatch repair-deficient (dMMR) phenotype of colorectal cancer.

methodsPatients with resectable dMMR colorectal cancer were eligible for inclusion. The prognostic and predictive value of CDX2 expression on the presence of lymph node metastasis (LNM) and survival was investigated. CDX2 status was determined via immunohistochemistry using the Leica Bond™ CDX2 (clone EP25) ready-to-use primary antibody.

resultsSome 235 of 238 consecutive dMMR tumours were assessed for CDX2 status. CDX2- was observed in 15·7 per cent of colorectal cancer. Interobserver agreement was excellent (

conclusionCDX2- does not confer a worse prognosis in the dMMR phenotype of colorectal cancer. The MMR status of patients with colorectal cancer should be determined before assessing CDX2 status.

Identifiers

PMID30511046
PMCPMC6253792
OpenAlexW2883195574

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.