New Onset of DiabetEs in aSsociation with pancreatic ductal adenocarcinoma (NODES Trial): protocol of a prospective, multicentre observational trial.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
19 11 2020
Historique:
entrez: 14 1 2021
pubmed: 15 1 2021
medline: 11 3 2021
Statut: epublish

Résumé

Pancreatic ductal adenocarcinoma (PDAC) has a dismal prognosis with an overall 5-year survival of approximately 8%. The success in reducing the mortality rate of PDAC is related to the discovery of new therapeutic agents, and to a significant extent to the development of early detection and prevention programmes. Patients with new-onset diabetes mellitus (DM) represent a high-risk group for PDAC as they have an eightfold higher risk of PDAC than the general population. The proposed screening programme may allow the detection of PDAC in the early, operable stage. Diagnosing more patients in the curable stage might decrease the morbidity and mortality rates of PDAC and additionally reduce the burden of the healthcare. This is a prospective, multicentre observational cohort study. Patients ≥60 years old diagnosed with new-onset (≤6 months) diabetes will be included. Exclusion criteria are (1) Continuous alcohol abuse; (2) Chronic pancreatitis; (3) Previous pancreas operation/pancreatectomy; (4) Pregnancy; (5) Present malignant disease and (6) Type 1 DM. Follow-up visits are scheduled every 6 months for up to 36 months. Data collection is based on questionnaires. Clinical symptoms, body weight and fasting blood will be collected at each, carbohydrate antigen 19-9 and blood to biobank at every second visit. The blood samples will be processed to plasma and analysed with mass spectrometry (MS)-based metabolomics. The metabolomic data will be used for biomarker validation for early detection of PDAC in the high-risk group patients with new-onset diabetes. Patients with worrisome features will undergo MRI or endoscopic ultrasound investigation, and surgical referral depending on the radiological findings. One of the secondary end points is the incidence of PDAC in patients with newly diagnosed DM. The study has been approved by the Scientific and Research Ethics Committee of the Hungarian Medical Research Council (41085-6/2019). We plan to disseminate the results to several members of the healthcare system includining medical doctors, dietitians, nurses, patients and so on. We plan to publish the results in a peer-reviewed high-quality journal for professionals. In addition, we also plan to publish it for lay readers in order to maximalise the dissemination and benefits of this trial. ClinicalTrials.gov NCT04164602.

Identifiants

pubmed: 33444177
pii: bmjopen-2020-037267
doi: 10.1136/bmjopen-2020-037267
pmc: PMC7678370
doi:

Banques de données

ClinicalTrials.gov
['NCT04164602']

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e037267

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: BK and AMG are employees of Metanomics Health GmbH, Germany.

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Auteurs

Dóra Illés (D)

First Department of Medicine, University of Szeged Faculty of Medicine, Szeged, Hungary.

Emese Ivány (E)

First Department of Medicine, University of Szeged Faculty of Medicine, Szeged, Hungary.

Gábor Holzinger (G)

First Department of Medicine, University of Szeged Faculty of Medicine, Szeged, Hungary.

Klára Kosár (K)

First Department of Medicine, University of Szeged Faculty of Medicine, Szeged, Hungary.

M Gordian Adam (MG)

Tegeler Weg 33, 10589, Metanomics Health GmbH, Berlin, Germany.

Beate Kamlage (B)

Tegeler Weg 33, 10589, Metanomics Health GmbH, Berlin, Germany.

Gábor Zsóri (G)

First Department of Medicine, University of Szeged Faculty of Medicine, Szeged, Hungary.

Máté Tajti (M)

First Department of Medicine, University of Szeged Faculty of Medicine, Szeged, Hungary.

Márk M Svébis (MM)

Department of Internal Medicine, Semmelweis University of Medicine, Budapest, Hungary.

Viktor Horváth (V)

Department of Internal Medicine, Semmelweis University of Medicine, Budapest, Hungary.

Ilona Oláh (I)

Ilona Tóth Outpatient Clinic, Budapest, Hungary.

Katalin Márta (K)

Institute for Translational Medicine, University of Pécs Medical School, Pécs, Hungary.
János Szentágothai Research Center, University of Pécs, Pécs, Hungary.

Szilárd Váncsa (S)

Institute for Translational Medicine, University of Pécs Medical School, Pécs, Hungary.
János Szentágothai Research Center, University of Pécs, Pécs, Hungary.

Noémi Zádori (N)

Institute for Translational Medicine, Pecsi Tudomanyegyetem Altalanos Orvostudomanyi Kar, Pecs, Hungary.

Andrea Szentesi (A)

Institute for Translational Medicine, Pecsi Tudomanyegyetem Altalanos Orvostudomanyi Kar, Pecs, Hungary.
MTA-SZTE Translational Gastroenterology Research Group, Szegedi Tudomanyegyetem, Szeged, Hungary.

Bálint Czakó (B)

Medical School, University of Szeged Faculty of Medicine, Szeged, Hungary.

Péter Hegyi (P)

Institute for Translational Medicine, Pecsi Tudomanyegyetem Altalanos Orvostudomanyi Kar, Pecs, Hungary.

László Czakó (L)

First Department of Medicine, University of Szeged, Szeged, Hungary czako.laszlo@med.u-szeged.hu.

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