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TerminatedNCT04007640PAIR-PANCREASUpdated Aug 12, 2026

Early Screening of Pancreatic Lesions : Development of New Imaging Tools

An interventional study of MRI with additional sequences and MRI in Pancreatic Cancer, sponsored by Assistance Publique - Hôpitaux de Paris. Terminated at 1 site in France. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-12.

Sponsored by Assistance Publique - Hôpitaux de Paris · Not applicable, Interventional, and Diagnostic

Why this study was terminated
Population difficult to recruit; number of enrolled patients sufficient for analyses.
Phase
Not applicable
Study type
Interventional
Enrollment
41
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

Obesity, diabetes and metabolic syndrome (MS) have all been associated with increase of pancreatic cancer (PK) risk. The precise role of obesity and diabetes and the pathways involved in the early oncogenic phases of PK associated with MS are not well known. The investigators hypothesize that it is possible to decipher this specific "fat-fibrosis-neoplastic sequence", to develop new imaging tools adapted to follow its progression, to test the benefit of treatments to slow this sequence and prevent the development of PK in obese and diabetic patients.This project is in line with a prevention strategy, by planning to understand the physiopathological pathways involved in MS leading to PK, to develop tools useful to screen early precancerous lesions in order to diagnose and treat patients at high risk, before cancer involvement.

This clinical trial is part of the INCA PAIR PANCREAS project : Early stages of pancreatic cancer associated with obesity and metabolic syndrome:

prevention and screening tools - Imaging of fatty pancreas in humans: correlation with pathological analysis, which includes 3 main coordinated objectives an in vitro approach an in vivo approach and this study (clinical approach).

Read the detailed description

Translational approach with direct application to humans, to test specific imaging MRI sequences in obese patients.

Obesity and metabolic syndrome are a well-known risk factor of pancreatic cancer. Obesity is associated with about 30% increased risk in all studies, but the proportion of obese people varies considerably from one country to another. Therefore, the proportion of cancer attributable to obesity could range from 3% to 16%. Numerous epidemiological studies confirmed that obesity is a risk factor of pancreatic cancer in obese men and women (BMI, kg/m2≥30.0), with a relative risk estimated to 1.76 (95% CI, 0.90-3.45) and 1.70 (95% CI, 1.09-2.64), respectively. As previously demonstrated by partners 9 and 10, obesity is associated with fat pancreatic infiltration and precancerous lesions, such as PanIN lesions in humans. Pancreatic lesions such as adipose infiltration, iron deposits, extent of fibrosis, acino-ductal metaplasia and Pan-IN are involved in pancreatic oncogenesis.

The goal of this study is to be able to diagnose early precancerous states in patients, such as acino-ductal metaplasia (and also PanIN lesions which are more frequently observed in humans,) inflammatory process (iron deposits, fibrosis lesions) and adipose involvement in the context of obesity and metabolic syndrome. Investigators hypothesis is that specific MR imaging sequences, adapted from previous studies in rodents, could be a relevant tool to diagnose early pancreatic lesions and follow their evolution in the context of obesity and metabolic syndrome.

To this aim, the investigators will conduct a study to assess the relevance of MR imaging sequences to diagnose specific pancreatic lesions in obese patients, validated at the microscopic level. The investigators will analyze MR imaging of obese patients (BMI>30)/non obese patients (BMI\<25) with a planned pancreatic surgery. It will be possible to compare imaging with histology performed on resected parenchyma. The investigators propose a proof-of-concept study aiming at assessing the relevance of specific MR imaging to diagnose early pancreatic lesions in humans and in obese patients especially. MR imaging will be performed in both obese and non obese patients with a planned pancreatic surgery in hospital to resect a benign lesion (such as neuroendocrine tumour or IPMN...). MRI are performed in the normal course of care; their sequences will be adapted for this study. It will be possible to compare imaging with histology of the resected parenchyma.

02

Conditions studied

  • Pancreatic Cancer

Keywords

  • Obesity
  • Diabetes
  • metabolic syndrome
  • Magnetic Resonance imaging,
  • Pancreatic Cancer
  • preneoplastic lesions
  • acino-ductal metaplasia,
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In context

Pancreatic Neoplasms

3,235 studies on the registry are indexed under Pancreatic Neoplasms; 899 are open to participants now.

This study's enrollment of 41 is below the median of 46 across 2,424 interventional studies indexed under Pancreatic Neoplasms.

Browse Pancreatic Neoplasms studies →

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,505 studies on the registry; 1,006 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 1st stage : Volunteers without history of known pancreatic disorders

    - Adults

  • 2nd stage : Obese Volunteers

    • Adults with planned hepatic MRI
    • Obese (BMI ≥30)
  • 3rd stage : Patients

    • Adults (aged 18-65 years) with a planned pancreatic surgery for benign pancreatic lesions (IPMN, cystic lesions or neuroendocrine tumors)
    • Obese (BMI≥30), overweight (25≤BMI≤29.9) or non-obese patients (18.5\<BMI\<24.9)

Exclusion criteria

Exclusion Criteria:

For volunteers without history of known pancreatic disorders (1st stage):

- Symptoms or past medical history suggesting pancreatic disorders

For all participants (1st, 2nd and 3rd stages) :

  • Patients with contraindication to MRI (pacemaker, claustrophobia…)
  • Inability to undergo MRI due to weight excess
  • Pregnant or breastfeeding woman
  • Absence of free and informed consent
  • Non affiliation to a social security regime or CMU
  • Subject deprived of freedom, subject under a legal protective measure
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
41 participants (actual)

Study arms

  • Other
    Volunteer patient

    1st stage: To adjust the transducer, test and validate pancreatic MRI sequences on volunteers without history of known pancreatic disorders. Adjustment of MRI parameters is needed to optimize data acquisition, especially in obese patients. Moreover, an external material (transducer) has to be applied on the abdomen. The right position has to be tested and specified before stages 2 and 3 of the study. We aim to include volunteers without history of known pancreatic disorders for the Stage 1, meaning volunteers without personal history or symptoms suggesting pancreatic disorders.

    Radiation: MRI

  • Other
    Obese volunteers with indication for hepatic MRI

    2nd stage: To validate and assess pancreatic MRI sequences on obese volunteers with indication for hepatic MRI , in relation with acceptable resolution and field of view criteria applicable to the typical anteroposterior diameters found in obese persons. For Magnetic Resonance Elastography (MRE), the amplitude setting of the MRE transducer will be adapted to the size of obese patients, in addition to the aforementioned adjustments to spatial resolution and field of view sizes. The effect of frequency on MRE data quality will be investigated. The effects of respiratory motion will be investigated; indeed in obese patients respiration amplitude is typically low and this enables to acquire data in free breathing mode over long periods of time, which offers more possibilities (notably in terms of averaging, spatial resolution, mechanical wave sampling rate) than when constraining acquisition parameters with a maximum breath hold time of less than 20s.

    Radiation: MRI with additional sequences

  • Other
    Obese patient

    3rd stage: To assess the relevance of MRI to diagnose specific pancreatic lesions in obese patients validated at the microscopic level. We will analyze MRI of obese patients and non-obese patients with a planned pancreatic surgery. It will be possible to compare imaging with histology performed on resected parenchyma

    Procedure: Left pancreatectomy or pancreaticoduodenectomy · Radiation: MRI with additional sequences

  • Other
    Non obese patients

    3rd stage: To assess the relevance of MRI to diagnose specific pancreatic lesions in obese patients validated at the microscopic level. We will analyze MRI of obese patients and non-obese patients with a planned pancreatic surgery. It will be possible to compare imaging with histology performed on resected parenchyma

    Procedure: Left pancreatectomy or pancreaticoduodenectomy · Radiation: MRI with additional sequences

  • Other
    Overweight patients

    3rd stage: To assess the relevance of MRI to diagnose specific pancreatic lesions in obese patients validated at the microscopic level. We will analyze MRI of obese patients and non-obese patients with a planned pancreatic surgery. It will be possible to compare imaging with histology performed on resected parenchyma

    Procedure: Left pancreatectomy or pancreaticoduodenectomy · Radiation: MRI with additional sequences

Interventions

  • RadiationMRI with additional sequences

    MRI with 15 min additional sequences to validate and assess pancreatic MRI sequences

  • RadiationMRI

    MRI with 15 min additional sequences to validate and assess pancreatic MRI sequences

  • ProcedureLeft pancreatectomy or pancreaticoduodenectomy

    Histological analysis :

  • RadiationMRI with additional sequences

    MRI with 15 min additional sequences to assess the relevance of MRI to diagnose specific pancreatic lesions in obese patients

06

What researchers measure

Primary outcomes

  1. Quantitative MRI parameters

    Pancreatic fat content

    Time frame: Day 1

  2. Quantitative MRI parameters

    Diffusion coefficients (10-4 mm2/s)

    Time frame: Day 1

  3. Quantitative MRI parameters

    transverse magnetization relaxation rate

    Time frame: Day 1

  4. Quantitative MRI parameters

    longitudinal relaxation rate

    Time frame: Day 1

  5. Quantitative MRI parameters

    visco-elastic parameters by measure of tissue stiffness (kPa)

    Time frame: Day 1

  6. fibroinflammatory lesions at histology in obese patients

    % surface of fibrosis

    Time frame: 2 months

  7. fibroinflammatory lesions at histology in obese patients

    % surface of acinoductal metaplasia

    Time frame: 2 months

  8. fibroinflammatory lesions at histology in obese patients

    number of acinoductal metaplasia lesions

    Time frame: 2 months

Secondary outcomes

  1. Histologic parameters

    % surface of fat pancreatic infiltration

    Time frame: 2 months

  2. Histologic parameters

    % surface of iron deposit

    Time frame: 2 months

  3. Histologic parameters

    % surface of fibrosis

    Time frame: 2 months

  4. Histologic parameters

    % surface of acinoductal metaplasia

    Time frame: 2 months

  5. Histologic parameters

    number of PanIN lesions

    Time frame: 2 months y

  6. MRI parameters

    pancreatic fat content

    Time frame: Day 1

  7. MRI parameters

    Diffusion coefficients (10-4 mm2/s)

    Time frame: Day 1

  8. MRI parameters

    transverse magnetization relaxation rate

    Time frame: Day 1I

  9. MRI parameters

    longitudinal magnetization relaxation rate

    Time frame: Day 1

  10. MRI parameters

    visco-elastic parameters by measure of tissue stiffness (kPa)

    Time frame: Day 1

  11. Biomarkers of pathways activation measured by immunohistochemistry on resected pancreatic parenchyma

    % expression of molecules involved in TGFb and orexin signaling

    Time frame: 2 months

  12. Biomarkers of pathways activation measured by immunohistochemistry on resected pancreatic parenchyma

    % expression of the markers in inflammatory cells (CD8, IL6, Caspase, HNF6)

    Time frame: 2 months

  13. Biomarkers of pathways activation measured by immunohistochemistry on resected pancreatic parenchyma

    % surface of acinoductal metaplasia

    Time frame: 2 months

  14. Biomarkers of pathways activation measured by immunohistochemistry on resected pancreatic parenchyma

    % of stained cells

    Time frame: 2 months

07

Study locations

1 site
  • Hôpital Beaujon
    Clichy, France
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04007640
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
National Cancer Institute, France, Ligue contre le cancer, France, Fondation ARC
Responsible party
Sponsor
First posted
Jul 5, 2019
Start date
Jun 18, 2019
Primary completion
May 31, 2023
Completion
May 31, 2023
Last update
Aug 12, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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