SARVADS 1: Assessment of the Prevalence of Sarcopenia by CT Scan in Patients Diagnosed With Head & Neck Cancer

Sponsor
Weprom (Other)
Overall Status
Recruiting
CT.gov ID
NCT04804852
Collaborator
(none)
50
1
19
2.6

Study Details

Study Description

Brief Summary

Sarcopenia is defined by the reduction in skeletal muscle mass and physical performance. It results in a decrease in muscle strength, overall physical activity, walking and the development of balance disorders and falls. It is one of the natural consequences of aging and contributes to frailty and the appearance of geriatric syndrome (s) (Chandapasirt et al, 2015; Cruz-Jentoft et al, 2010).

Its prevalence in patients with Head & Neck cancer is 39% (Hua et al, 2020) and is associated with an increase in postoperative complications (Achim et al, 2017; Bril et al, 2019), with greater toxicity of chemotherapy. (Wendrich et al, 2017) and reduced overall survival (Hua et al, 2020).

It is measured by CT scan (assessment of muscle volume with respect to L3 using IMAGE J software) (Teigen et al, 2018) and by clinical tests (performance tests) (Swartz et al, 2016, Cruz-Jentoft et al, 2010).

Several studies have shown a possible assessment of sarcopenia by measuring skeletal muscle mass with regard to C3 (Ufuk et al, 2019; Swartz et al, 2016).

This trial aims to evaluate the prevalence of sarcopenia in head and neck cancer evaluated by CT at C3.

Condition or Disease Intervention/Treatment Phase
  • Other: sarcopenia assessment

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Assessment of the Prevalence of Sarcopenia by CT Scan in Patients Diagnosed With Head & Neck Carcinoma
Actual Study Start Date :
Oct 29, 2020
Anticipated Primary Completion Date :
May 30, 2022
Anticipated Study Completion Date :
May 30, 2022

Arms and Interventions

Arm Intervention/Treatment
study population

Patient diagnosed with head & neck carcinoma at diagnosis

Other: sarcopenia assessment
evaluation of sarcopenia by CT san at the C3 vertebrae

Outcome Measures

Primary Outcome Measures

  1. Assessment of the prevalence of sarcopenia by cervical CT scan (C3) [6 months]

    Number of patients with sarcopenia at diagnosis and during treatments

Secondary Outcome Measures

  1. Assessment of hypoalbuminemia [6 month]

    Number of patients presenting an hypoalbuminemia.

  2. De- and undernutrition [6 month]

    Number of patients with a BMI <18 and with a prescription for nutritional complements.

  3. Compliance to the treatment [6 months]

    Number of patients having the complete planned treatment

  4. complete response rate [6 months]

    Number of patients with a complete response on the end-of-treatment evaluation scanner according to the RECIST or PERCIST criteria in the numerator out of the total number of patients in the denominator

  5. Assessment of hospitalizations treatment-related complications [6 months]

    Number of hospitalizations per patient for treatment-related complications

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patient over 18 years old,

  • affiliated to the social security scheme,

  • suffering from locally advanced head & neck cancer (stages I to IVB) at diagnosis,

  • not operable,

  • justifying treatment by radiotherapy, whether or not associated with chemotherapy or targeted therapy (eg: monoclonal antibodies, immunotherapy) whatever the proposed modalities.

Exclusion Criteria:
  • patient treated by non-conservative surgery and cervical lymph node dissection making it impossible to assess muscle mass with regard to C3,

  • metastatic disease,

  • minor patient,

  • adult patient under guardianship,

  • pregnancy or breastfeeding in progress.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinique Victor Hugo / Centre Jean Bernard Le Mans France 72000

Sponsors and Collaborators

  • Weprom

Investigators

  • Study Director: LE DU Katell, MD, Weprom

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Weprom
ClinicalTrials.gov Identifier:
NCT04804852
Other Study ID Numbers:
  • WP-2020-04
First Posted:
Mar 18, 2021
Last Update Posted:
Oct 8, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 8, 2021