About this trial
To observe the efficacy and toxicities of heavy ion radiation therapy for locally advanced or advanced primary thymic epithelial malignant tumor received R2 resection. The primary endpoint was progression-free survival and toxicities, and the secondary endpoint was local relapse-free survival, overall survival and cause-specific survival.
Eligibility criteria
Qualifiers
Patients with stage II-IV (Masaoka-Koga) thymus epithelial malignancies without a history of thoracic radiotherapy who had undergone radical surgery (R2 resection, visible residual tumor) and had a definite pathological diagnosis.
Sign informed consent.
Between the ages of 18 and 70.
ECOG general status score of 0-2.
Disqualifiers
Complicated with other malignant tumors that have not been controlled.
Have large quantity of pleural or pericardial effusion.
Patient whose particle radiotherapy plan cannot meet the minimum target dose coverage and dose volume limitation requirements, or cannot meet the dose constrains of normal tissue or organs.
Chest radiation therapy or radioactive particle implantation history.
Trial design
Treatments tested in this trial
- Carbon ion radiotherapy
- combined with platinum-based regimen
Treatment groups
Locations
1Sponsors and collaborators
Jian Chen
Lead sponsor
Shanghai Proton and Heavy Ion Center
Sponsor institution