Evaluation of the Efficacy and Safety of Local Cryotherapy Treatment of Recurrent Head and Neck Cancer in Irradiated Areas: a Pilot Study (CRYORL)
Recurrent Head and Neck Cancer, Local Cryotherapy Treatment
About this trial
This is an interventional treatment trial for Recurrent Head and Neck Cancer
Eligibility Criteria
Inclusion Criteria: Malignant head/neck tumor Unresectable locoregional recurrence in a previously irradiated area Contraindication to re-irradiation Age > 18 years Performance index ≤ 2 (WHO) Life expectancy > 12 weeks Absence of hemostasis disorders Renal function: creatinine clearance ≥ 30 mL/min by CKD-EPI method (Cockcroft-Gault formula or MDRD) Subject affiliated to a social security health insurance plan Subject able to understand the objectives and risks of the research and to give dated and signed informed consent For a woman of childbearing age, negative blood pregnancy test at the inclusion visit Exclusion Criteria: Stage IV with distant metastases or multiple tumors Melanoma, sarcoma, and lymphoma Participants who have received chemotherapy or radiation therapy within 4 weeks Other active cancer within the past 2 years (patients with carcinoma in situ, papillary thyroid carcinoma, basal cell skin carcinoma, localized Gleason 6 prostate cancer, or breast cancer in situ are allowed) Concomitant therapy with any other systemic anticancer treatment Contraindication of anaesthesiology character Contraindication to MRI Participation in another clinical study Any social, medical or psychological condition that may prevent the patient from complying with the constraints of the protocol Any significant pathology that may interfere with the patient's participation in the study Subject under court protection Subject under guardianship or curatorship Pregnant or breastfeeding women
Sites / Locations
- Hôpitaux Universitaires de Strasbourg
Arms of the Study
Arm 1
Experimental
local cryotherapy treatment