Evidence map›Paper›PMID 24721904›Full record

ArticleGut2015

The combination of autofluorescence endoscopy and molecular biomarkers is a novel diagnostic tool for dysplasia in Barrett's oesophagus.

Massimiliano di Pietro, David F Boerwinkel, Mohammed Kareem Shariff, Xinxue Liu, Emmanouil Telakis, Pierre Lao-Sirieix, Elaine Walker, George Couch, Leanne Mills, Tara Nuckcheddy-Grant and 9 more

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Gut, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

24 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Review
  3. Agrin Loss in Barrett's Esophagus-Related Neoplasia and Its Utility as a Diagnostic and Predictive Biomarker.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. A biomarker panel predicts progression of Barrett's esophagus to esophageal adenocarcinoma.Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus · 2019
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Role of endoscopy in early oesophageal cancer.Nature reviews. Gastroenterology & hepatology · 2016
    Review
  15. Endoscopic modalities for the diagnosis of Barrett's oesophagus.United European gastroenterology journal · 2016
    Review
  16. Article
  17. Article
  18. Review
  19. Article
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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

19 authors at 5 institutions in 2 countries.

Massimiliano di PietroMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
David F BoerwinkelDepartment of Gastroenterology, Academic Medical Centre, Amsterdam, The Netherlands.
Mohammed Kareem ShariffMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
Xinxue LiuMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
Emmanouil TelakisMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK Department of Gastroenterology, Academic Medical Centre, Amsterdam, The Netherlands Digestive Disease Centre, NIHR Biomedical Research Unit, Nottingham University Hospitals NHS trust, Nottingham, UK Department of Pathology, Academic Medical Center, Amsterdam, The Netherlands Department of Pathology, Nottingham University Hospitals NHS Trust, Nottingham, UK Biostatistics Unit, Medical Research Council, Cambridge, UK.
Pierre Lao-SirieixMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
Elaine WalkerMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
George CouchMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
Leanne MillsMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
Tara Nuckcheddy-GrantMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
Susan SliningerDigestive Disease Centre, NIHR Biomedical Research Unit, Nottingham University Hospitals NHS trust, Nottingham, UK.
Maria O'DonovanMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
Mike VisserDepartment of Pathology, Academic Medical Center, Amsterdam, The Netherlands.
Sybren L MeijerDepartment of Pathology, Academic Medical Center, Amsterdam, The Netherlands.
Philip V KayeDepartment of Pathology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Lorenz WernischBiostatistics Unit, Medical Research Council, Cambridge, UK.
Krish RagunathDigestive Disease Centre, NIHR Biomedical Research Unit, Nottingham University Hospitals NHS trust, Nottingham, UK.
Jacques J G H M BergmanDepartment of Gastroenterology, Academic Medical Centre, Amsterdam, The Netherlands.
Rebecca C FitzgeraldMedical Research Council, Cancer Unit, University of Cambridge, Cambridge, UK.
Medical Research Council · GBAcademic Medical Center · NLUniversity of Cambridge · GBNottingham University Hospitals NHS Trust · GBMRC Cancer Unit · GB

Funding

Department of Health NIHR-RP-02-12-011Medical Research Council MC_U105260799Medical Research Council MC_U105365007Medical Research Council MC_UU_12022/2
6 · The paper itself

Abstract

objectiveEndoscopic surveillance for Barrett's oesophagus (BO) is limited by sampling error and the subjectivity of diagnosing dysplasia. We aimed to compare a biomarker panel on minimal biopsies directed by autofluorescence imaging (AFI) with the standard surveillance protocol to derive an objective tool for dysplasia assessment.

designWe performed a cross-sectional prospective study in three tertiary referral centres. Patients with BO underwent high-resolution endoscopy followed by AFI-targeted biopsies. 157 patients completed the biopsy protocol. Aneuploidy/tetraploidy; 9p and 17p loss of heterozygosity; RUNX3, HPP1 and p16 methylation; p53 and cyclin A immunohistochemistry were assessed. Bootstrap resampling was used to select the best diagnostic biomarker panel for high-grade dysplasia (HGD) and early cancer (EC). This panel was validated in an independent cohort of 46 patients.

resultsAneuploidy, p53 immunohistochemistry and cyclin A had the strongest association with dysplasia in the per-biopsy analysis and, as a panel, had an area under the receiver operating characteristic curve of 0.97 (95% CI 0.95 to 0.99) for diagnosing HGD/EC. The diagnostic accuracy for HGD/EC of the three-biomarker panel from AFI+ areas was superior to AFI- areas (p<0.001). Compared with the standard protocol, this panel had equal sensitivity for HGD/EC, with a 4.5-fold reduction in the number of biopsies. In an independent cohort of patients, the panel had a sensitivity and specificity for HGD/EC of 100% and 85%, respectively.

conclusionsA three-biomarker panel on a small number of AFI-targeted biopsies provides an accurate and objective diagnosis of dysplasia in BO. The clinical implications have to be studied further.

Indexed as

EsophagoscopyAdultAgedAged, 80 and overBarrett EsophagusBiomarkersCross-Sectional StudiesFemaleHumansImage-Guided BiopsyMaleMiddle AgedOptical ImagingProspective StudiesBiomarkersBarrett's OesophagusDysplasiaEndoscopyOesophageal CancerSurveillance

Identifiers

PMID24721904
PMCPMC4283667
OpenAlexW2154123622

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.