Role of Myostatin, Activin A and Follistatin Cachexia of ENT Cancers
NCT ID: NCT03162042
Last Updated: 2017-05-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
60 participants
OBSERVATIONAL
2015-11-02
2017-05-31
Brief Summary
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Detailed Description
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55 patients were included in the study : 32 in the cancer group (only squamous cell carcinoma) and 23 in the control group. The patients underwent a complete nutritional assessment and multiple samples : blood before and 7 days after surgery, skeletal muscle biopsies, tumor biopsies. Plasma concentrations of myostatin, activin and follistatin were measured before and after tumor removal surgery. Concentrations of myostatin, activin and follistatin were also measured in an incubation medium of a tumor biopsy. Activin A and follistatin plasma concentrations were significantly increased in the cancer group (320 vs. 203 pg/ml ; p \<0.001) (3593 vs 2148 pg/ml ; p \<0.001), while myostatin plasma concentration was significantly decreased in this group (1542 vs. 2100 pg/ml ; p = 0.010). Surprisingly, data of the 7th postoperative day showed an increase in plasma activin A concentration (379 vs 320 pg /ml ; p \<0.001) while concentrations of myostatin and follistatin were not modified. A high postoperative systemic inflammation is one hypothesis to explain these later results. Myostatin, activin A and follistatin proteins were systematically detected in the medium of tumor a 48 hour-incubation period, providing a strong proof of the tumor production of these factors by squamous cell carcinoma. The activin A/myostatin/follistatin is modified in the context of head and neck cancer. Activin A particularly seems to play a role in the occurrence of cachexia while follistatin could have a protective role for skeletal muscle mass. This system could aimed in therapeutic ways to reduce cachexia in a context of cancer in order to improve the quality of life and survival of patients.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Squamous cell carcinoma
55 patients were included in the study : 32 in the cancer group (only squamous cell carcinoma) and 23 in the control group.
Tumor removal
Surgery
Control group
55 patients were included in the study : 32 in the cancer group (only squamous cell carcinoma) and 23 in the control group.
Tumor removal
Surgery
Interventions
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Tumor removal
Surgery
Eligibility Criteria
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Inclusion Criteria
* head and neck cancer
* squamous cell carinoma only
* head and neck surgery chosen as treatment of cancer
* age 18-75
For control group :
* Neck surgery for non oncologic disease
* age 18-75
Exclusion Criteria
* cachexia for control group
18 Years
75 Years
ALL
Yes
Sponsors
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University Hospital, Clermont-Ferrand
OTHER
Responsible Party
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Locations
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CHU Clermont-Ferrand
Clermont-Ferrand, Auvergne, France
Countries
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Other Identifiers
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2015-A00833-46
Identifier Type: OTHER
Identifier Source: secondary_id
CHU-326
Identifier Type: -
Identifier Source: org_study_id
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