Head and Neck Squamous Cell Carcinomas (HNSCCs) Clinical Trial
— EGéSOROfficial title:
Impact of Comprehensive Geriatric Assessment on Malnutrition, Functional Status and Survival in Elderly Patients With Head and Neck Squamous Cell Carcinomas (HNSCCs): a Randomized Controlled Multicenter Clinical Trial
| Verified date | November 2020 |
| Source | Assistance Publique - Hôpitaux de Paris |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The intervention tested in this research project aims to reduce this inequality by improving the management of elderly head and neck cancer patients with a specific management. Indeed, the treatment of elderly head and neck cancer patients has specificities concerning treatment options, their tolerance, psychological management, nutritional and functional status, and support needed at home. To assess the overall needs of the elderly patients, an assessment known as "comprehensive geriatric assessment" (CGA) can be performed by a geriatrician with extensive testing and questionnaires. This assessment is long and requires an experienced geriatrician. It leads to the development of an individualized treatment plan (physiotherapy, psychological follow-up, support at home, nutritional management ...) and follow-up to adapt the necessary cares for the duration of the cancer treatment. The CGA utility has been studied in elderly patients with nonmalignant diseases. Studies have shown that CGA allowed improving survival and maintaining the elderly at home.
| Status | Completed |
| Enrollment | 499 |
| Est. completion date | September 2020 |
| Est. primary completion date | April 2018 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 65 Years and older |
| Eligibility | Inclusion Criteria: - patients aged 65 years old and over (modified by amendment n 2 -1/07/2014) - macroscopical lesions suggesting an cancerous tumor in head and neck awaiting pathology confirmation; - support in one of ENT/Maxilla-facial surgery departments in the study; - patients insured by a social security; - patients informed of the study, and having given his non opposition verbally. Exclusion Criteria: - patients deprived of liberty or under legal protection; - presence of psychological, family, socials or geographic condition(s) that may interfere with the proper conduct of the study; - personal history of head and neck cancer except single surgery for squamos cell carcinoma without additional treatment (without curietherapy or RT) with a free interval of at least 5 years (modified by amendment n 2 -1/07/2014) - patients with cancerous tumor of sinus and salivary glands |
| Country | Name | City | State |
|---|---|---|---|
| France | Centre Hospitalier Intercommunal de Créteil / Hopital Henri Mondor | Créteil |
| Lead Sponsor | Collaborator |
|---|---|
| Assistance Publique - Hôpitaux de Paris | Cancéropole Ile De France, National Cancer Institute (NCI) |
France,
Abstracts of the 6th European Congress of Oto-Rhino-Laryngology Head and Neck Surgery, June 30-July 4, 2007, Vienna, Austria. Eur Arch Otorhinolaryngol. 2007 Jun;264 Suppl 1:S1-354. — View Citation
Homma A, Sakashita T, Oridate N, Suzuki F, Suzuki S, Hatakeyama H, Mizumachi T, Taki S, Fukuda S. Importance of comorbidity in hypopharyngeal cancer. Head Neck. 2010 Feb;32(2):148-53. doi: 10.1002/hed.21158. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Composite criteria, including: death; autonomy (if loss of two points or more in the Activity of Daily Living (ADL) compared with the initial ADL); nutritional status (if weight loss of 10% or more compared to the initial weight at diagnosis | 6 months after the randomization | ||
| Secondary | progression-free survival | 6 month, 12 month and 24 month after the randomization | ||
| Secondary | death | 6 month , 12 month and 24 month after the randomization | ||
| Secondary | total duration of hospitalization | 6 month, 12 month and 24 month after the randomization | ||
| Secondary | quality of life (QLQC30, HN35) | 6 month , 12 month and 24 month after the randomization | ||
| Secondary | costs of treatment | 6 month , 12 month and 24 month after the randomization |