Assessment of the Prevalence of Sarcopenia by CT Scan in Patients Diagnosed With Head & Neck Cancer (SARVADS 1)
Assessment of the Prevalence of Sarcopenia by CT Scan in Patients Diagnosed With Head & Neck Carcinoma
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.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Forventet)
Kontakter og plasseringer
Studiekontakt
- Navn: Magali BALAVOINE
- Telefonnummer: 0033 241682940
- E-post: m.balavoine@weprom.fr
Studer Kontakt Backup
- Navn: Jonas DUBU
- E-post: jonas.dubu@i-l-c.fr
Studiesteder
-
-
-
Le Mans, Frankrike, 72000
- Rekruttering
- Clinique Victor Hugo / Centre Jean Bernard
-
Ta kontakt med:
- Jonas DUBU
- Telefonnummer: +33 769510938
- E-post: jonas.dubu@i-l-c.fr
-
Hovedetterforsker:
- Katell Le Dû, MD
-
Hovedetterforsker:
- Amandine RUFFIER, MD
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
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.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Observasjonsmodeller: Kohort
- Tidsperspektiver: Potensielle
Kohorter og intervensjoner
Gruppe / Kohort |
Intervensjon / Behandling |
|---|---|
|
study population
Patient diagnosed with head & neck carcinoma at diagnosis
|
evaluation of sarcopenia by CT san at the C3 vertebrae
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Assessment of the prevalence of sarcopenia by cervical CT scan (C3)
Tidsramme: 6 months
|
Number of patients with sarcopenia at diagnosis and during treatments
|
6 months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Assessment of hypoalbuminemia
Tidsramme: 6 month
|
Number of patients presenting an hypoalbuminemia.
|
6 month
|
|
De- and undernutrition
Tidsramme: 6 month
|
Number of patients with a BMI <18 and with a prescription for nutritional complements.
|
6 month
|
|
Compliance to the treatment
Tidsramme: 6 months
|
Number of patients having the complete planned treatment
|
6 months
|
|
complete response rate
Tidsramme: 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
|
6 months
|
|
Assessment of hospitalizations treatment-related complications
Tidsramme: 6 months
|
Number of hospitalizations per patient for treatment-related complications
|
6 months
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Studieleder: LE DU Katell, MD, Weprom
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- WP-2020-04
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .