HNSCC
Conditions
Keywords
salivary glands, sinus carcinoma, radiochemotherapy concomitant, cisplatin, protontherapy
Brief summary
A phase III, multicenter, randomized, open-label, french study comparing: * Arm A : Radiotherapy alone (66 to 70 Gy; 5 fractions/week; 1fraction/day; 2 Gy/fraction) (IMRT or protontherapy) * Arm B: Radiotherapy (66 to 70 Gy; 5 fractions/week; 1fraction/day; 2 Gy/fraction; IMRT or protontherapy) + concomitant cisplatin 100 mg/m2 IV on day 1 - J22 - 43 (3 cycles)
Detailed description
Carcinomas of the sinuses and the salivary glands are rare. They are heterogeneous in terms of anatomical sites and histology subtypes. For this reason and in the absence of prospective study, their treatment is still largely extrapolated from data of frequent carcinomas of the upper digestive tract. These tumors are most often diagnosed lately. Their treatment is based on a multimodal management of care, with a central place for the surgery and radiotherapy (Proof level Grade C). Despite the advances in surgical techniques, and the addition of radiation therapy, the 5-year overall survival probability does not exceed 65% mainly due to a loco regional development. In this context, a chemotherapy administered concomitantly to radiotherapy, could increase the efficacy of the locoregional treatment by a radiosensibilization process and regardless of the histology. This point is regularly discussed in multidisciplinary concertation meeting, including bi-monthly national REFCOR meeting (network of French Expertise on rare Cancers of the head and neck). At present, the lack of data brings even to discuss the addition of cisplatin to exclusive irradiation of unresectable or not operable tumors. No randomized study has been published in this context. The first comparative prospective study addressing the addition of weekly cisplatin to the adjuvant irradiation of salivary, is a phase II randomized study (Radiation Therapy Oncology Group - RTOG 1008) currently enrolling patients in the United States of America. The Sponsor propose to conduct a phase III randomized study evaluating the impact of the addition of cisplatin to a treatment by radiotherapy in adjuvant setting (≥ 65 Gy) in case of a high risk of recurrence: case of radioresistant histologies (e.g. cystic fibrosis adenoids carcinomas), or case of unfavourable histo-prognostic criteria (incomplete resection, presence of emboli, etc.) in this population.
Interventions
DRUGCisplatin
intravenous, concomitant to irradiation
RADIATIONradiotherapy
66 à 70 Gy per fractions of 2 Gy, 1 fraction/day, 5 fractions/week
Sponsors
National Cancer Institute, France
Groupe Oncologie Radiotherapie Tete et Cou
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
\- Resected tumors of the sinus or the salivary glands T3-4, N1-3 or T1-2 N0, with overgrown banks or positive margins (\< 5 mm) or Unresectable or not operable tumors of salivary glands or sinuses * Carcinomas of the main salivary glands (parotid, submandibular or sublingual glands) and accessories or Malignant sinus tumors with any histological type except melanoma, lymphoma, mesenchymal tumor (sarcoma type), squamous cell carcinoma and nasopharyngeal carcinoma type 1, 2, 3. * Age ≥ 18 years * Performance status 0 -2 (WHO criteria) * For patients ≥ 70 years, the score to the G8 questionnaire must be \> 14 with no fall in the previous 12 months or with a geriatric assessment consistent with the administration of chemotherapy * Estimated life expectancy greater than or equal to 6 months * Neutrophils \> 1.5 x 109/l, platelets \> 100 x 109/l, hemoglobin ≥ 9.5 g/dl, bilirubin ≤ 3 x upper normal value (ULN), AST/ALT \< 5 ULN, PAL \< 3 ULN * Creatinin Clearance ≥ 60 mL/min (Cockroft formula) * Adequate cardiac function according to the investigator, compatible with the administration of cisplatin 100 mg/m² * Affiliation to a social insurance or beneficiary of such a regimen * Patient having given his written consent signed before any study specific procedure.
Exclusion criteria
* History of radiotherapy in the ENT region and/or neoadjuvant chemotherapy for the pathology concerned * Synchronous metastases * Contraindications for administration of cisplatin or carboplatin * Allergy to cisplatin and/or its excipients * Vaccination against yellow fever, recent or planned * Administration of phenytoin with prophylactic purpose * Other cancer, except for cancer in situ of the cervix, skin Carcinoma (except melanoma) or cancer controlled for more than 5 years * Pregnant, breastfeeding or without birth control woman. Woman having the ability to procreate should have (serum or urinary) negative pregnancy test within 14 days prior to study treatment decision-making. (Men or women) patients should use a reliable contraceptive method throughout the treatment and at least 6 months after the end of chemotherapy. * Persons deprived of liberty under supervision or under curatorship, or unable to adhere to medical follow-up of the study for geographical, social or psychological reasons.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free survival | From date of randomization to date of disease progression or death, which occur first, assessed during 62 months | Compare progression-free survival between the 2 treatment arms: radiation therapy alone versus radiochimiotherapy in adjuvant patients treatment operated. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall Survival | From date of randomization to date of death, assessed during 62 months | Compare the 2 arms of treatment in operated patients in terms of overall survival |
Other
| Measure | Time frame | Description |
|---|---|---|
| Assessment of quality of Life: QLQC30 overall score | From date of randomization to end of study or death or progression (the first occurred), assessed during 62 months | Compare quality of life (QLQC30 overall score) between arms |
Countries
France
Outcome results
None listed