Early Screening of Pancreatic Lesions : Development of New Imaging Tools (PAIR-PANCREAS)
Pancreatic Cancer
About this trial
This is an interventional diagnostic trial for Pancreatic Cancer focused on measuring Obesity, Diabetes, metabolic syndrome, Magnetic Resonance imaging,, Pancreatic Cancer, preneoplastic lesions, acino-ductal metaplasia,
Eligibility Criteria
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:
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
Sites / Locations
- Hôpital Beaujon
- Hôpital BeaujonRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Other
Other
Other
Other
Other
Volunteer patient
Obese volunteers with indication for hepatic MRI
Obese patient
Non obese patients
Overweight patients
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.
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.
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
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
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