Evidence map›Paper›PMID 40180412›Full record

Observational studyBMJ open2025

European Registry of Hereditary Pancreatic Diseases (EUROPAC): protocol for primary and secondary screening in individuals with inherited pancreatic disease syndromes for pancreatic ductal adenocarcinoma and complications of other pancreatic diseases.

Annabelle Boughey, Phil Hopley, Ioannis Sarantitis, Paul Thomas, Beata Gubacsi, Kayleigh Jevons, Emma Crowe, Eleri Hughes, Isobel Quinn, Liam Royle and 3 more

Abstract readObservational Study
In one paragraph

Observational study in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

13 authors.

Annabelle BougheyMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Phil HopleyMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Ioannis SarantitisMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Paul ThomasMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Beata GubacsiMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Kayleigh JevonsMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Emma CroweMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Eleri HughesMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Isobel QuinnMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Liam RoyleMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Richard J JacksonLiverpool Clinical Trials Centre, University of Liverpool, Liverpool, UK.
William GreenhalfMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Chris HalloranMolecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK halloran@liverpool.ac.uk.ORCID http://orcid.org/0000-0002-5471-4178

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPancreatic cancer is a devastating disease and one of the top causes of cancer death worldwide. Over 30% of cases are potentially avoidable, and while screening for this disease should be possible, the current methods, without risk stratification to detect high-risk groups, are unlikely to detect these individuals. A tailored screening pathway could be applied to individuals with a germline genetic cause of pancreatic cancer, which may account for around 10% of cases. METHODS AND ANALYSIS: EUROPAC, although having international reach, is described here in relation to the UK only. This national prospective observational study has run for several decades but was modified into the current trial in 2019, which aims to recruit and screen 10 000 individuals with either familial pancreatic cancer or hereditary pancreatitis (HP). Applicants are assessed for eligibility by generating an individual pedigree and by attributing a family risk score (FR). Individual risk is assessed according to age. Individuals over 40 with an FR >30 are offered baseline imaging and then three yearly triplets of annual endoscopic ultrasound (EUS) and an MRI (in the third year). Those with an FR >60 are offered both EUS and MRI yearly. HP patients are screened by CT and/or MRI dependent on risk stratification using the presence of diabetes, smoking or alcohol consumption. Low-risk (absence of these factors) patients have a CT every 2 years, and high-risk (one or more of the above factors) patients have alternate yearly screening with CT, then MRI. Biospecimens are collected at pragmatic intervals with first sampling at registration to support future biomarker development to detect pancreatic cancer early. Detection of early-stage pancreatic cancer and actionable lesions will be evaluated. ETHICS AND DISSEMINATION: The EUROPAC study has been reviewed and approved by the Yorkshire and Humber Research Ethics Committee (Ref 19/YH/0250). Study results will be disseminated through national and international symposium presentations and published in peer-reviewed, open-access journals. All participants provided informed consent prior to entering the study. TRIAL REGISTRATION NUMBER: ISRCTN62546421.

Indexed as

Carcinoma, Pancreatic DuctalEarly Detection of CancerPancreatic NeoplasmsPancreatitisAdultCarcinomaEndosonographyEuropeFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedPancreatitis, ChronicProspective StudiesRegistriesCancer geneticsPancreatic diseasePancreatic surgeryREGISTRIES

Identifiers

PMID40180412
PMCPMC11969613

What OpenQuestion holds

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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.