Descrizione riassuntiva della sperimentazione (Fonte di dati: BASEC)
La présente étude a pour objectif d'évaluer l'efficacité de l'ajout de nivolumab (immunothérapie) au traitement standard de référence pour un cancer de la bouche ou de la gorge précédemment traité par chirurgie qui présente un risque élevé de rechute.
Le traitement standard combine la radiothérapie (traitement par les rayons X) et la chimiothérapie par cisplatine.
Le nivolumab est un anticorps monoclonal anti-PD-1, capable de stimuler la réponse immunitaire contre les cellules tumorales. Cette efficacité a été observée pour des cancers de la bouche ou de la gorge à un stade très avancé. Cette étude a pour but d’évaluer si un bénéfice peut aussi être observé dans une situation nettement moins évoluée.
Ainsi, l'étude comparera les données de deux groupes de patients. Le premier groupe recevra le traitement standard (radiothérapie+cisplatine) et le deuxièeme groupe recevra le traitement standard + le nivolumab. Les participants seront distribués au hasard dans l'un de ces deux groupes et en seront informés avant le début du traitement.
Malattie studiate(Fonte di dati: BASEC)
cancer épidermoïde localement avancé de la tête et du cou
Health conditions
(Fonte di dati: WHO)
Squamous Cell Carcinoma of Head and Neck
Malattia rara
(Fonte di dati: BASEC)
No
Interventi esaminati (p. es. medicamento, terapia, campagna)
(Fonte di dati: BASEC)
Traitement combinant le nivolumab (immunothérapie) au traitement standard cisplatine (chimiothérapie) + radiothérapie
- Bras A: radiothérapie+cisplatine
- Bras B: nivolumab+radiothérapie+cisplatine
Interventions
(Fonte di dati: WHO)
Drug: Cisplatin
Drug: Nivolumab
Radiation: RT
Criteri per la partecipazione alla sperimentazione
(Fonte di dati: BASEC)
- Agé de 18 à 75 ans
- Statut de performance ECOG de 0 ou 1
- Cancer épidermoïde de la tête et du cou histologiquement confirmé (cavité orale, oropharynx ou larynx)
Criteri di esclusione
(Fonte di dati: BASEC)
- Cancer du nasopharynx, des sinus paranasaux, tumeurs de la cavité nasale ou cancer de la tyroïde
- Cancer incluant des ganglions lymphatiques du cou avec un site primaire inconnu
- Cancer métastatique
Inclusion/Exclusion Criteria
(Fonte di dati: WHO)
Inclusion Criteria:
1. Age > 18 and < 75 years
2. Performance Status (PS) ECOG 0-1 (Appendix 2)
3. Written informed consent
4. Recording of alcohol consumption and smoking history
5. Stage III, stage IV (American Joint Committee on Cancer 7th edition) 38
6. Oral cavity, oropharynx, hypopharynx or larynx
7. Squamous cell carcinoma treated by primary surgery
8. Recovery from the surgical procedure allowing for cisplatin-RT
9. RT planned within 4 to 8 weeks after surgery
10. Patient/tumor carrying a high risk of relapse with:
- extra-capsular extension (ECE),
- and/or positive margins (R1 or close margin = 1 mm)
11. Availability of surgical tumour specimen (PD-L1, TILs and immune landscape ...)
12. For oropharyngeal tumor, known p16 status (by IHC)
13. Determination of patient ability to receive cisplatin 100 mg/m2 for 3 cycles:
- Calculated creatinine clearance = 60 mL/min as determined by CKD-EPI method
(Cockcroft and Gault or MDRD method allowed)
- Absolute neutrophil count =1 500/µL, platelets =100 000/µL, haemoglobin = 10
g/dL, aspartate (AST) and alanine transaminase (ALT) less than 2 times the upper
limit of the normal range (ULN), total bilirubin = 1.5 mg/dL, serum albumin >35
g/L
- Peripheral neuropathy = grade 1
- Sensorineural hearing loss (confirmed by audiogram)
- Cardiac function compatible with hyperhydration
- No administration of prophylactic phenytoin
- For ppatients aged 71-74 years, PS must be 0 and fit according to geriatric
evaluation
Exclusion Criteria:
1. Nasopharyngeal, paranasal sinuses, nasal cavity tumours or thyroid cancers
2. Squamous cell carcinoma involving cervical neck nodes with unknown primary site
3. Metastatic disease (stage IVc)
4. Active viral infection (HIV, Hepatitis B/C) or known history of positive test for HIV
5. Active autoimmune disease
6. Active immunodeficiency or ongoing immunosuppressive therapy
7. Active CNS disease
8. Interstitial lung disease
9. Active infection
10. Any prior or current treatment for invasive head and neck cancer. This will include
but is not limited to: prior tyrosine kinase inhibitors, any monoclonal antibody,
induction chemotherapy, prior RT, or use of any investigational agent
11. Concurrent treatment with any other systemic anti-cancer therapy that is not specified
in the protocol
12. Concomitant treatment with any drug on the prohibited medication list such as live
vaccines. Live vaccines administered more than 30 days before study entry are
permitted
13. History of other malignancy within the last 3 years (exception of in situ carcinoma,
thyroid papillary carcinoma, skin carcinomas, localized prostate carcinoma Gleason 6
and in situ breast carcinoma)
14. Pregnant, breastfeeding patients, and female patients of childbearing potential who
are unwilling or unable to use 2 highly effective methods of contraception as outlined
in the protocol for the duration of the study and for at least 6 months after the last
dose of cisplatin and 7 months after the last dose of nivolumab
15. Significant disease which, in the judgment of the investigator, as a result of the
medical interview, physical examinations, or screening investigations would make the
patient inappropriate for entry into the trial
16. Known hypersensitivity reaction to study drugs
17. Any social, personal, medical and/or psychologic factor(s) that could interfere with
the observance of the patient to the protocol and/or the follow-up and/or the
signature of the informed consent
18. Prior organ transplantation including allogenic stem-cell transplantation
19. Clinically significant (i.e., active) cardiovascular disease: cerebral vascular
accident/stroke (< 6 months prior to enrollment), myocardial infarction (< 6 months
prior to enrollment), unstable angina, congestive heart failure (= New York Heart
Association Classification Class II), or serious cardiac arrhythmia requiring
medication
20. Persisting toxicity related to prior therapy or pre-existing conditions (NCI CTCAE v.
4.03 Grade > 1) 39
21. Other severe acute or chronic medical conditions including colitis, pneumonitis,
pulmonary fibrosis or psychiatric conditions including active suicidal ideation; or
laboratory abnormalities that may increase the risk associated with study
participation and, in the judgment of the investigator, would make the patient
inappropriate for entry into this study
22. Concurrent enrolment in another clinical trial using an investigational anti-cancer
treatment within 28 days prior to the first dose of study treatment
Minimum age: 18 Years
Maximum age: 74 Years
Sex: All
-
Altre informazioni sulla sperimentazione
Data di registrazione della sperimentazione
1 giu 2018
Inserimento del primo partecipante
10 ott 2018
Stato di reclutamento
Recruiting
Titolo scientifico
(Fonte di dati: WHO)
A Phase III Randomized Trial of Post-operative Adjuvant Nivolumab and Concomitant Chemo-radiotherapy in High-risk Patients With Resected Squamous Cell Carcinoma of Head and Neck
Tipo di sperimentazione
(Fonte di dati: WHO)
Interventional
Disegno della sperimentazione
(Fonte di dati: WHO)
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
Fase
(Fonte di dati: WHO)
Phase 3
Punti finali primari
(Fonte di dati: WHO)
Disease free survival
Punti finali secondari
(Fonte di dati: WHO)
Acute toxicity
Late toxicity
Overall survival
Contatto per informazioni
(Fonte di dati: WHO)
Please refer to primary and secondary sponsors
Risultati della sperimentazione
(Fonte di dati: WHO)
Sintesi dei risultati
ancora nessuna informazione disponibile
Collegamento ai risultati nel registro primario
ancora nessuna informazione disponibile
Informazioni sulla disponibilità dei dati dei singoli partecipanti
ancora nessuna informazione disponibile
Siti di esecuzione della sperimentazione
Siti di esecuzione in Svizzera
(Fonte di dati: BASEC)
Losanna
Paesi di esecuzione
(Fonte di dati: WHO)
È possibile che la Svizzera non appaia ancora come paese di esecuzione perché non è ancora stata registrata nel registro primario dell’OMS.
France
Contatto per maggiori informazioni sulla sperimentazione
Dati della persona di contatto in Svizzera
(Fonte di dati: BASEC)
Dr Petr Szturz
+41795567667
petr.szturz@chuv.ch
Contatto per informazioni generali
(Fonte di dati: WHO)
Jean BOURHIS, Pr
(0)21 314 46 66
jean.bourhis@chuv.ch
Contatto per informazioni scientifiche
(Fonte di dati: WHO)
Joël GUIGAY, MD
04 92 03 15 01
Joel.Guigay@nice.unicancer.fr
Autorizzazione da parte della commissione d’etica (Fonte di dati: BASEC)
Nome della commissione d’etica che rilascia l’autorizzazione (nel caso di studi multicentrici solo la commissione direttiva)
Commission
cantonale d’Éthique de la Recherche sur l’être humain Vaud (CER-VD)
Data di autorizzazione da parte della commissione d’etica
10.03.2020
Altri numeri di identificazione delle sperimentazioni
Numero di identificazione della sperimentazione della commissione d’etica (BASEC-ID)
(Fonte di dati: BASEC)
2019-02292
Secondary ID (Fonte di dati: WHO)
GORTEC 2018-01
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