Evidence map›Paper›PMID 30106834›Full record

Trial reportJournal of clinical gastroenterology2019

The Diagnostic Yield of Malignancy Comparing Cytology, FISH, and Molecular Analysis of Cell Free Cytology Brush Supernatant in Patients With Biliary Strictures Undergoing Endoscopic Retrograde Cholangiography (ERC): A Prospective Study.

Vladimir M Kushnir, Daniel K Mullady, Koushik Das, Gabriel Lang, Thomas G Hollander, Faris M Murad, Sara A Jackson, Nicole A Toney, Sydney D Finkelstein, Steven A Edmundowicz

Abstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical gastroenterology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Observational
  9. Article
  10. Review
  11. Review
  12. The Diagnostic Dilemma of Malignant Biliary Strictures.Diagnostics (Basel, Switzerland) · 2020
    Review
  13. Review
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

10 authors.

Vladimir M KushnirDepartment of Medicine, Division of Gastroenterology, Washington University School of Medicine, St Louis, MO.
Daniel K MulladyDepartment of Medicine, Division of Gastroenterology, Washington University School of Medicine, St Louis, MO.
Koushik DasDepartment of Medicine, Division of Gastroenterology, Washington University School of Medicine, St Louis, MO.
Gabriel LangDepartment of Medicine, Division of Gastroenterology, Washington University School of Medicine, St Louis, MO.
Thomas G HollanderDepartment of Medicine, Division of Gastroenterology, Washington University School of Medicine, St Louis, MO.
Faris M MuradDepartment of Medicine, Division of Gastroenterology, Washington University School of Medicine, St Louis, MO.
Sara A JacksonInterpace Diagnostics Corporation, Pittsburgh, PA.
Nicole A ToneyInterpace Diagnostics Corporation, Pittsburgh, PA.
Sydney D FinkelsteinInterpace Diagnostics Corporation, Pittsburgh, PA.
Steven A EdmundowiczDepartment of Medicine, Division of Gastroenterology, Washington University School of Medicine, St Louis, MO.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRoutine cytology of biliary stricture brushings obtained during endoscopic retrograde cholangiopancreatography (ERCP) has suboptimal sensitivity for malignancy. We compared the individual and combined ability of cytology, fluorescence in situ hybridization (FISH) analysis and PCR-based mutation profiling (MP) to detect malignancy in standard biliary brushings.

methodsWe performed a prospective study of patients undergoing ERCP using histology or 1 year follow-up to determine patient outcomes. MP was performed on free-DNA from biliary brushing specimens using normally discarded supernatant fluid. MP examined KRAS point mutations and tumor suppressor gene associated loss of heterozygosity mutations at 10 genomic loci. FISH examined chromosome specific gains or losses.

resultsA total of 101 patients were included in final analysis and 69% had malignancy. Cytology had 26% sensitivity and 100% specificity for malignancy. Using either FISH or MP in combination with cytology increased sensitivity to 44% and 56%, respectively. The combination of all 3 tests (cytology, FISH, and MP) had the highest sensitivity for malignancy (66%). There was no difference in the specificity of cytology, FISH or MP testing when examined alone or in combination. MP improved diagnostic yield of each procedure from 22% to 100%; FISH improved yield to 90%. MP detected 21 malignancies beyond that identified by cytology; FISH detected an additional 13. The combination of FISH and MP testing detected an additional 28 malignancies.

conclusionsBoth MP and FISH are complimentary molecular tests that can significantly increase detection of biliary malignancies when used in combination with routine cytology of standard biliary brush specimens.

Indexed as

Cholangiopancreatography, Endoscopic RetrogradeAdultAgedAged, 80 and overBiliary Tract NeoplasmsCell-Free SystemCholestasisCytodiagnosisFemaleHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedMutationPolymerase Chain ReactionProspective Studies

Identifiers

PMID30106834
PMCPMC6768606

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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.