Evidence map›Paper›PMID 42015571›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2026

Diagnostic and Prognostic Values of Bile Biomarkers for Malignant Biliary Stenosis.

E Gigante, V Untereiner, S Caruso, R Rhaiem, L Grados, C Boulagnon-Rombi, S Adam, G D Sockalingum, R Garnotel, G Thiefin

Abstract read
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Diagnostic and Prognostic Values of Bile Biomarkers for Malignant Biliary Stenosis.Liver international : official journal of the International Association for the Study of the Liver · 2026
    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

10 authors.

E GiganteCHU Reims, Service D'hépato-Gastroentérologie et De Cancérologie Digestive, Reims, France.ORCID 0000-0002-5455-2308
V UntereinerUniversité De Reims Champagne-Ardenne, URCATech, PICT, Reims, France.
S CarusoUniversité Paris Est Créteil, INSERM, IMRB, Créteil, France.
R RhaiemCHU de Reims, Service de Chirurgie Digestive, Reims, France.
L GradosCHU D'amiens, Service De Gastroentérologie Et D'oncologie Digestive, Amiens, France.
C Boulagnon-RombiCHU De Reims, Service De Pathologie; Medyc Umr 7369, Université De Reims Champagne-Ardenne, Reims, France.
S AdamUniversité De Reims Champagne-Ardenne, BioSpecT-UR7506, Reims, France.
G D SockalingumUniversité De Reims Champagne-Ardenne, BioSpecT-UR7506, Reims, France.
R GarnotelUniversité De Reims Champagne-Ardenne, BioSpecT-UR7506, Reims, France.
G ThiefinUniversité De Reims Champagne-Ardenne, BioSpecT-UR7506, Reims, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDifferentiating between malignant and benign biliary strictures remains a clinical challenge because current diagnostic tools have limited sensitivity. The detection of tumour-related biomarkers directly in bile, which is in close contact with the lesion, may enhance diagnostic accuracy. This study aimed at evaluating the diagnostic and prognostic values of biliary concentrations of VEGF, PDGF-AA, IGF and MMPs in patients with extrahepatic cholangiocarcinoma (CCA), pancreatic ductal adenocarcinoma (PDAC), or benign obstruction.

methodsA total of 100 consecutive patients undergoing ERCP for obstructive jaundice were enrolled and categorised into benign (n = 48), CCA (n = 23) and PDAC (n = 29) groups. Bile samples collected during ERCP were analysed. The diagnostic and prognostic performance of several biomarkers was assessed and, when appropriate, their incremental diagnostic value was assessed in comparison with standard bile cytology.

resultsBiliary concentrations of VEGF, MMP-1, MMP-2, MMP-7 and MMP-9 were significantly higher in malignant cases than in benign cases. VEGF demonstrated the best diagnostic accuracy (AUROC 0.86, sensitivity 87%, specificity 81%). MMP-1 and MMP-7 also showed good diagnostic values (AUROCs 0.79 and 0.81 respectively). In the multivariate analysis, VEGF was independently associated with the diagnosis of malignancy and PDAC, whereas both VEGF and MMP-2 were independently associated with CCA diagnosis. Using a predefined cut-off, bile VEGF showed a higher sensitivity than bile cytology, and their combination markedly reduced false-negative results. Regarding prognosis, higher PDGF-AA levels were independently associated with better survival rates.

conclusionBiliary VEGF is a strong independent biomarker for the diagnosis of malignant biliary obstruction, both in PDAC and CCA. MMP-2 was independently associated with CCA diagnosis. PDGF-AA is a promising prognostic biomarker for malignant biliary strictures. These findings support the clinical potential of bile-based biomarkers for improving the diagnosis and assessing the prognosis of malignant biliary strictures.

Indexed as

BileBile Duct NeoplasmsBiomarkers, TumorCarcinoma, Pancreatic DuctalCholangiocarcinomaCholestasisPancreatic NeoplasmsAgedAged, 80 and overCholangiopancreatography, Endoscopic RetrogradeFemaleHumansMaleMatrix MetalloproteinasesMiddle AgedPlatelet-Derived Growth FactorBiomarkers, TumorMatrix MetalloproteinasesPlatelet-Derived Growth Factorplatelet-derived growth factor AVascular Endothelial Growth Factor Abile biomarkerscholangiocarcinomadiagnosispancreatic adenocarciomaprognosis

Identifiers

PMID42015571
PMCPMC13100460

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.