Tests carbon ion radiotherapy against standard radiation for hard-to-treat tumors

Trial details

Who runs it

Hospices Civils de Lyon

Trial code

NCT02838602

Record updated

2 September 2021

Original description

This is a transnational prospective randomized trial comparing definitive carbon ion therapy versus photon or combined photon and protontherapy as standard treatment for unresectable or macroscopically uncompleted resected radioresistant tumors. Eligible tumors are axial chordoma (except of base of skull), adenoid cystic carcinoma of head and neck (except of trachea) and sarcomas of any site (except chondrosarcoma of the skull base), non previously irradiated and without pre-planned surgery or chemotherapy after the clinical trial procedure. Randomization is balanced 1 for 1. Patients of the experimental arm are treated in carbon ions centers in Europe and patients of the standard arm are treated in France in their closest participating radiotherapy center. An accrual of 250 patients is needed and an absolute difference of 20% of relapse free survival at five years is awaited. The main endpoint is the progression free survival at five years. The trial is supported by the French program of clinical research and the national health insurance. Two associated studies are carried out: a radiobiological one looking for radioresistance markers in the sarcomas biopsies, and the second one is about medico economics.Read full original descriptionShow less

Transnational Randomized Study Comparing Carbon Ions Therapy Versus Conventional Radiotherapy - Including Protontherapy - for the Treatment of Radioresistant Tumors

This is a transnational prospective randomized trial comparing definitive carbon ion therapy versus photon or combined photon and protontherapy as standard treatment for unresectable or macroscopically uncompleted resected radioresistant tumors. Eligible tumors are axial chordoma (except of base of skull), adenoid cystic carcinoma of head and neck (except of trachea) and sarcomas of any site (except chondrosarcoma of the skull base), non previously irradiated and without pre-planned surgery or chemotherapy after the clinical trial procedure. Randomization is balanced 1 for 1. Patients of the experimental arm are treated in carbon ions centers in Europe and patients of the standard arm are treated in France in their closest participating radiotherapy center. An accrual of 250 patients is needed and an absolute difference of 20% of relapse free survival at five years is awaited. The main endpoint is the progression free survival at five years. The trial is supported by the French program of clinical research and the national health insurance. Two associated studies are carried out: a radiobiological one looking for radioresistance markers in the sarcomas biopsies, and the second one is about medico economics.

Inclusion: age ≥ 18 years; No severe comorbidity, life expectancy above 10 years; Unresectable or inoperable or R2 resection of the tumor; Eligible radioresistant tumor according to the limitative list as following:; adenoid cystic carcinoma of head and neck (larynx and trachea excluded); soft tissue sarcoma; pleomorphic rhabdomyosarcoma only (alveolar and embryonal forms excluded); retroperitoneal sarcoma under condition of technical feasibility (movement); osteosarcoma of any grade and localisation (Ewing excluded); chondrosarcoma (except of skull base) OMS grade >= 2; chordoma axial skeleton or pelvis (except of skull base); angiosarcoma; Absence of epidermal invasion (a hypodermic invasion is accepted with fixity of cutaneous plan but not true epidermal permeation); Larger volume to be irradiated (PTV) less than 25 cm; ECOG Performance Status ≤ 2 or Karnovsky index ≥ 60; no pregnancy of possibility of pregnancy during the treatment; having an health insurance; signature of a written informed consent; validation of the randomization criteria: namely, a carbon ions therapy indication assessed by the medical team of a hadrontherapy center and able to by treated within two month from registration.

Exclusion: Complete macroscopic or microscopic surgical resection (R0 or R1); previous irradiation in the volume to be treated; any contra-indication to undergo a radiation therapy by Xray or particle therapy; planned surgery or chemotherapy to take place after completion of radiotherapy (example : absence of enough space between an organ risk and the target volume (at least 5 mm) except the possibility of a spacer insertion); planned surgery or chemotherapy after radiotherapy; metastatic disease; disease not candidate to a curative approach (example accelerated progressive diseaseresistant to nay medical treatment especially for sarcoma); history of concomittant (except in situ cervix carcinoma; or any cured basocellular cutaneous cancer tor any cured cancer with no sign of relapse during 5 years)); Presence in the target volume of metallic material which cannot be removed (carbon fibres matreial authorized); impossible follow-up over 5 years.

ClinicalTrials.gov NCT02838602