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Clinical Trials/NCT05606523
NCT05606523RecruitingNot Applicable

Can Fecal Microbiota Transplantation of Cachectic Patients with Pancreas Cancer Impair Body Weight Gain in Germ-free Mice? the EXTRA Study

Genton Graf Laurence1 site in 1 country24 target enrollmentStarted: August 1, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
24
Locations
1
Primary Endpoint
Body weight changes in mice after fecal material transplantation.

Study Overview

Brief Summary

This monocentric study aims at evaluating the effects of fecal microbiota transplantation from newly diagnosed cachectic and non-cachectic pancreatic cancer patients, and healthy volunteers on several cachexia-related parameters of germ-free mice.

Detailed Description

Aim: Evaluating the effects of fecal microbiota transplantation (FMT) from 6 newly diagnosed cachectic and 6 non-cachectic pancreatic cancer patients, and 12 healthy age-and sex-matched volunteers on several cachexia-related parameters of 96 germ-free mice (4 per donor) over a 30-day period. The fecal material of all 12 pancreatic cancer patients will be collected at diagnosis before any cancer treatment onset.

Hypothesis

FMT of cachectic patients with pancreas cancer, naïve of any anti-cancer treatment and artificial nutrition, into germ-free mice impairs weight gain, in contrast to FMT of non-cachectic patients and healthy controls.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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 the last 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 <15 kg/m2 in women) 81, and not by CT, as it is faster and can be performed at the bedside of the patient. Non-cachectic pancreatic cancer patients (n=6)
  • Normal nutritional state: weight stability (± 2% of habitual weight) over the last 6 months, no anorexia before the diagnosis (appetite rating on a visual analogue scale of 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 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 major surgery 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

Outcomes

Primary Outcomes

Body weight changes in mice after fecal material transplantation.

Time Frame: Between days 0 and 30

Body weight (g)

Secondary Outcomes

  • Muscle mass(at diagnosis)
  • Nutritional intake(at diagnosis)
  • Homeostatic model assessment (HOMA)-score(at diagnosis)
  • Differences in fecal microbiota(at diagnosis)
  • Glycemia(at diagnosis)
  • Body weight(at diagnosis)
  • Resting energy expenditure (REE)(at diagnosis)
  • Waist-to-hip ratio(at diagnosis)
  • Fat mass(at diagnosis)
  • Fat-free mass(at diagnosis)
  • Appetite(at diagnosis)
  • Insulinemia(at diagnosis)
  • Physical activity(at diagnosis)
  • Mortality(at diagnosis)
  • Physical function(at diagnosis)
  • Quality of life(at diagnosis)
  • Epithelial permeability(at diagnosis)
  • Oral microbiota(at diagnosis)
  • GALT function and systemic inflammation(at diagnosis)

Investigators

Sponsor
Genton Graf Laurence
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Genton Graf Laurence

Principal Investigator

University Hospital, Geneva

Study Sites (1)

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