About this trial
This project proposes to elucidate the functional impact of T cells in cancer progression and treatment through a comprehensive TCR profiling study and a longitudinal cohort study in patients with advanced epithelial ovarian cancer. Our findings aim to provide clinical insights for monitoring treatment response in a non-invasive way and demonstrate the association of TCR diversity with clinical outcomes and the potential role of TCR profiling in cancer prognosis.
Eligibility criteria
Qualifiers
Newly diagnosed patients with advanced EOC, 18-75 years of age: including patients with preoperative assessment of stage III-IV EOC, who underwent initial tumour cytoreduction and 6-8 courses of postoperative chemotherapy with paclitaxel + carboplatin/docetaxel + carboplatin;
Eastern Cooperative Oncology Group (ECOG) physical strength status (PS) score of 0 or 1;
Cooperation in the treatment process by providing clinicopathological data and imaging data required for the study process;
Cooperate with follow-up visits and collection of node blood for clinical efficacy assessment, and agree to use the test data for subsequent research and product development.
Disqualifiers
Neoadjuvant chemotherapy patients;
Splenectomy patients;
Patients with contraindications to radiotherapy;
Any other patients who, in the judgement of the investigator, may have poor compliance with the procedures and requirements of the study;
Trial design
Treatments tested in this trial
- Not listed