Study at the Man of the Profile of Chimiokines in the Anorexia Bound to the Cancerous Cachexy (CHIMIOKINES)

October 24, 2022 updated by: Centre Hospitalier Universitaire de Nice

Study at the Man of the Profile of Chimiokines in the Anorexia Bound to the Cancerous Cachexy.

The syndrome of anorexia-cachexie, which accompanies numerous cancers is a major comorbidity which compromises the forecast of these patients. Several cytokines pro-inflammatory as interleukines IL1 ß, IL6 or TNFa participate in the physiopathology of this syndrome at the man and the animal. Besides, it is now established that different neuronal populations, localized in the hypothalamus, are nerve centers of the control of the appetite and the energy homéostasie. However, there is not enough evidence of a direct action of cytokines on these neurones, suggesting the participation of intermediate molecules as chimiokines, inflammatory molecules produced in reaction to an immunological stress by gliales cells and acting directly on the surrounding neurones. The implication of chimiokines in the syndrome of anorexia-cachexie associated with the cancer thus seems very likely Among these, chimiokines " Monocyte Chemoattractant Proteins 1-3 " or MCPs represent obvious candidates because they are produced by multiple tumors. Furthermore, to the mouse, the intellectual expression of MCP1 is correlated in the anorexia led by peripheral injections of a bacterial by-product, the lipopolysaccharide (LPS).

The investigators' main objective is to test at the Man's, in situation of cancer of the pancreas any confused stages, the degree of prédictivité of the chimiokine MCP1 towards the syndrome of anorexia-cachexie associated with the cancer. The investigator also suggest describing: i) the link between rate plasmatique of MCP1 and energy metabolism on one hand, physical composition on the other hand;; ii) the impact of the other chimiokines, particularly those of the family of the MCPs, on the anorexia-cachexie bound to the cancer, iii) the correlation enters their profile of expression plasmatique and the severity of the anorexia, the energy metabolism and the physical composition; iv) the same research on the other inflammatory factors plasmatiques, of nature different from chimiokines; v) the correlation between thin mass and anorexia; vi) the evolution of the chimiokines various and inflammatory factors after surgical treatment or chemotherapy with curative aim in 6 months.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Nice, France, 06000
        • CHU de Nice

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Group 1 {cancer of the pancreas WITH syndrome of anorexia-cachexie}

Inclusion Criteria:

  • Patient to hospitalize in the unit of digestive cancer research.
  • Patient ≥ 18 years.
  • Patient carrier of an adénocarcinome of the pancreas of novo, any stadium confused, diagnosed by imaging and/or histology.
  • Existence of at least one of the criteria following to hold(retain) the diagnosis of cachexie cancer patient: not deliberate loss of weight > in 5 % over the last 6 months OR(WHERE) IMC(CEREBRAL-MOTOR HANDICAPPED) < 20 kg / m ² with a loss of minimum weight > 2 % OR(WHERE) scrawny muscular index appendiculaire respectively < 7,26 kg / m ² at the man and < 5,45 kg / m ² at the woman with a minimal weight loss > 2 %.
  • Patient having signed the enlightened consent.

Exclusion Criteria:

  • Patient having a tumor other one than the pancreatic adénocarcinome.
  • Patient having a second offense of adénocarcinome pancreatic.
  • Patient carrier of a pancreatic adénocarcinome in the course of a treatment by chemotherapy.
  • Patient having a severe psychiatric comorbidity except TCA who can be responsible for food disorders.
  • Patient carrier of an evolutionary inflammatory disease other one than the cancer being able to interfere on the inflammatory status.

Groupe 2 {cancer du pancréas SANS syndrome d'anorexie-cachexie}

Inclusion Criteria:

  • Patient to hospitalize in the(unit) of digestive cancer research.
  • Patient ≥ 18 years.
  • Patient carrier of an adénocarcinome of the pancreas of novo, any stadium confused, diagnosed by imaging and/or histology.
  • Patient having signed a enlightened consent.

Exclusion Criteria:

  • Patient having a tumor other one than the pancreatic adénocarcinome.
  • Patient having a second offense(recurrence) of adénocarcinome pancreatic.
  • Patient carrier of a pancreatic adénocarcinome in the course of a treatment by chemotherapy.
  • Existence of at least one of the criteria in favour of the diagnosis of cachexie cancer patient: not deliberate loss of weight > in 5 % over the last 6 months OR(WHERE) IMC(CEREBRAL-MOTOR HANDICAPPED) < 20 kg / m ² with a loss of minimum weight > 2 % OR(WHERE) scrawny muscular index appendiculaire respectively < 7,26 kg / m ² at the man and < 5,45 kg / m ² at the woman with a minimal weight loss > 2 %.
  • Patient having a severe psychiatric comorbidity except TCA who can be responsible for food disorders.
  • Patient carrier of an evolutionary inflammatory disease other one than the cancer being able to interfere on the inflammatory status.
  • Patient refusing to participate in the study
  • Under guardianship patient or guardianship.

Group 3 {pure food limitation typifies restrictive anorexia nervosa}

Inclusion Criteria:

  • Patient seen in consultation in the unit of nutritional support(medium)
  • Patient ≥ 18 years.
  • Patient carrier of an eating disorder of type pure restrictive anorexia nervosa (according to criterion diagnosis of the WHO)
  • Patient having signed a enlightened consent.

Exclusion Criteria:

  • Patient having any evolutionary organic pathology source of a decrease of the oral contributions and/or the interference on the inflammatory status, and responsible for a loss of weight
  • Patient refusing to participate in the study
  • Under guardianship patient or guardianship.

Group 4 {unhurt individual of any appetite-suppressing evolutionary disease and cachectisante}

Inclusion Criteria:

  • Patient seen in consultation of hepatogastroenterology
  • Patient ≥ 18 years.
  • Unhurt patient of any organic or psychic, evolutionary pathology, cachectisante
  • Patient having signed a enlightened consent.

Exclusion Criteria:

  • Patient refusing to participate in the study
  • Under guardianship patient or guardianship.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: groupe1
cancer of the pancreas WITH syndrome of anorexia-cachexie Dosage of chimiokines
Other: groupe2
cancer of the pancreas WITHOUT syndrome of anorexia-cachexie Dosage of chimiokines
Other: groupe3
pure food limitation typifies restrictive anorexia nervosa Dosage of chimiokines
Other: groupe4
unhurt individual of any appetite-suppressing evolutionary disease and cachectisante Dosage of chimiokines

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
chimiokine MCP1 expression
Time Frame: change from baseline to 180 days
Study at the Man's, in situation of cancer of the pancreas, diagnosed of novo and any confused stages, the prediction of the chimiokine MCP1 towards the syndrome of anorexia-cachexie associated with the cancer
change from baseline to 180 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Stéphane SCHNEIDER, Pr, Centre Hospitalier Universitaire de Nice

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2012

Primary Completion (Actual)

December 2, 2013

Study Completion (Actual)

December 24, 2019

Study Registration Dates

First Submitted

July 20, 2012

First Submitted That Met QC Criteria

July 8, 2016

First Posted (Estimate)

July 13, 2016

Study Record Updates

Last Update Posted (Actual)

October 26, 2022

Last Update Submitted That Met QC Criteria

October 24, 2022

Last Verified

October 1, 2022

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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