Phase
Condition
Pancreatic Cancer
Cancer
Digestive System Neoplasms
Treatment
N/AClinical Study ID
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients with pancreatic cancer (n=12)
≥18 years and
Newly diagnosed of pancreatic adenocarcinoma (local or metastatic) and
Tube feeding or parenteral nutrition ≤ 14 days
Cachectic pancreatic cancer patients (n=6)
Cachexia according to the Fearon criteria 1: involuntary weight loss >5% over thelast 6 months, or any level of weight loss >2% and a BMI <20 kg/m2 or sarcopenia.Sarcopenia will be diagnosed by BIA (fat-free mass index is <17 kg/m2 in men and <15kg/m2 in women) 81, and not by CT, as it is faster and can be performed at thebedside of the patient. Non-cachectic pancreatic cancer patients (n=6)
Normal nutritional state: weight stability (± 2% of habitual weight) over the last 6months, no anorexia before the diagnosis (appetite rating on a visual analogue scaleof 100mm), no known impaired glucose tolerance.
Healthy matched subjects (n=12)
≥18 years and
BMI between 18.5 and 30 kg/m2 and
Absence of chronic or acute disease and
Matching for gender and age (± 5 years) with an included pancreatic cancer patient
Exclusion
Exclusion Criteria:
< 18 years or
Inability to give consent or
Insufficient knowledge of project language (French, German) or
Pancreatic adenocarcinoma already treated by chemo- or radiotherapy, or majorsurgery as duodenopancreatectomy or biliary diversion
Known rheumatologic or immunologic diseases
Therapeutic antibiotics or immunosuppressive drugs (for instance glucocorticoids,cytostatics, antibodies) in the 30 days preceding the inclusion
Study Design
Study Description
Connect with a study center
Geneva University Hospitals
Geneva, 1211
SwitzerlandActive - Recruiting
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