Evidence map›Paper›PMID 42334072›Full record

ArticleInternational journal of cancer2026

Immune Markers and Risk of Pancreatic Cancer in the European EPIC Cohort.

Verena A Katzke, Yue Chen, Srimanti Dutta, Federico Canzian, Julie Louise Munk Andersen, Agnetha Linn Rostgaard-Hansen, Léa Bouteille, Vinciane Rebours, Thérèse Truong, Matthias B Schulze and 19 more

Abstract read
In one paragraph

Article in International journal of cancer, 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. 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

29 authors.

Verena A KatzkeDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID https://orcid.org/0000-0002-6509-6555
Yue ChenDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Srimanti DuttaDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Federico CanzianGenomic Epidemiology Group, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID https://orcid.org/0000-0002-4261-4583
Julie Louise Munk AndersenDanish Cancer Institute, Copenhagen, Denmark.
Agnetha Linn Rostgaard-HansenDanish Cancer Institute, Copenhagen, Denmark.
Léa BouteilleParis-Saclay University, UVSQ, Inserm, Gustave Roussy, CESP, Villejuif, France.
Vinciane ReboursDepartment of Pancreatology and Digestive Oncology, Beaujon Hospital, AP-HP, Paris-Cité University, Clichy, France.
Thérèse TruongParis-Saclay University, UVSQ, Inserm, Gustave Roussy, CESP, Villejuif, France.ORCID https://orcid.org/0000-0002-2943-6786
Matthias B SchulzeDepartment of Molecular Epidemiology, German Institute of Human Nutrition Potsdam-Rehbruecke, Nuthetal, Germany.
Benedetta BendinelliClinical Epidemiology Unit, Institute for Cancer Research, Prevention and Clinical Network-ISPRO, Florence, Italy.ORCID https://orcid.org/0000-0002-4796-1517
Valeria PalaEpidemiology and Prevention Unit, Fondazione IRCCS Istituto Nazionale Dei Tumori di Milano, Milan, Italy.ORCID https://orcid.org/0000-0001-5438-970X
Vittorio SimeonMedical Statistics Unit, University "L. Vanvitelli", Naples, Italy.
Rosario TuminoHyblean Association for Epidemiology Research, A.I.R.Ep. ETS, Ragusa, Italy.
Carlotta SacerdoteCentre for Biostatistics, Epidemiology, and Public Health (C-BEPH), Department of Clinical and Biological Sciences, University of Turin, Turin, Italy.
Roel VermeulenDivision of Environmental Epidemiology and Veterinary Public Health, Institute for Risk Assessment Sciences, Utrecht University, Utrecht, the Netherlands.
P Martijn KolijnDivision of Environmental Epidemiology and Veterinary Public Health, Institute for Risk Assessment Sciences, Utrecht University, Utrecht, the Netherlands.
Sjoerd G EliasDepartment of Epidemiology and Health Economics, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Marta Crous-BouUnit of Nutrition and Cancer, Cancer Epidemiology Research Program, Catalan Institute of Oncology (ICO)-Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Maria-José SánchezEscuela Andaluza de Salud Pública (EASP), Granada, Spain.
Ana Jimenez-ZabalaBiogipuzkoa Health Research Institute, Group of Epidemiology of Chronic and Communicable Diseases, San Sebastian, Gipuzkoa, Spain.
José María HuertaCentro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Marcela GuevaraCentro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Nick WarehamMRC Epidemiology Unit, University of Cambridge School of Clinical Medicine, Institute of Metabolic Science, Cambridge, UK.
Marie BreeurCancer Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Mattias JohanssonEarly Detection, Prevention, and Infections Branch (EPR), International Agency for Research on Cancer (IARC/WHO), Lyon, France.
James YarmolinskyImperial College London, London, UK.
Daniele CampaDepartment of Biology, University of Pisa, Pisa, Italy.ORCID https://orcid.org/0000-0003-3220-9944
Rudolf KaaksDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID https://orcid.org/0000-0003-3751-3929

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The immune system is a major driver in pancreatic cancer development. Several prospective cohort studies have found associations for single immune system-derived proteins such as IL6 or CRP, but results are inconclusive, and Omics-based research is scarce. Hence, we aimed to investigate associations of a comprehensive protein panel with the risk of pancreatic cancer. Within the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort, 92 immune proteins were measured in baseline blood samples of 406 incident pancreatic cancer cases and 406 sex- and age-matched controls, using the Olink Immuno-Oncology panel. Multivariable adjusted conditional logistic regression was used to estimate odds ratios (OR, 95% CI) for protein levels in association with pancreatic cancer risk. Eight biomarkers were associated with pancreatic cancer risk (MMP12, LAMP3, CD28, IL-6, IL-12, FASLG, PD-L2, and PDCD1) but only MMP12 was significantly associated after multivariable adjustments for confounders and the seven proteins, with OR = 1.56 (95% CI: 1.20-2.03) for a doubling in protein concentration. After correction for multiple testing, none of the proteins were associated with risk. Restricting analyses to cases diagnosed within the first 4 years and 4-8 years after recruitment resulted in OR of 1.89 (95% CI: 1.28-2.80) and 1.37 (95% CI: 1.01-1.86) for MMP12, respectively. Higher levels of MMP12 were associated with pancreatic cancer risk specifically in those diagnosed shortly after recruitment, while other immune-related factors were not associated with risk. Further cohort studies are needed to confirm our initial findings.

Indexed as

Biomarkers, TumorPancreatic NeoplasmsAgedCase-Control StudiesCohort StudiesEuropeFemaleHumansMaleMiddle AgedProspective StudiesRisk FactorsBiomarkers, TumorcohortEPICimmune markersimmune‐oncologyinflammationOlinkproteins

Identifiers

PMID42334072
PMCPMC13547983

What OpenQuestion holds

Textmetadata
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.