About this trial
To explore the non-inferiority of the 2y-OS rate of tislelizumab combined with chemotherapy after sequential CRT in the treatment of resectable esophageal squamous cell carcinoma compared with the surgical group
Eligibility criteria
Qualifiers
The subjects were included in this study and signed the informed consent form.
Male or female patients aged between 18 and 75 years old;
Patients diagnosed with esophageal squamous cell carcinoma by histopathology;
According to the 8th edition of the AJCC Esophageal cancer TNM staging system, it is located in cT2N+ or cT3-4aNanyM0 (confirmed by enhanced CT/MRI of the chest and abdomen), and the lesion is located in the thoracic segment.
Disqualifiers
There are clinically uncontrolled pleural effusions, pericardial effusions or ascites that require repeated drainage or medical intervention (within 2 weeks before randomization);
It is known that there is intolerance or resistance to the chemotherapy specified in the trial protocol;
Have received any other ESCC anti-tumor treatments (e.g., targeted treatments for PD-1, PD-L1, PD-L2, or other tumor immunotherapy, radiotherapy, targeted therapy, ablation, or other systemic or local anti-tumor treatments);
Patients with active autoimmune diseases or a history of autoimmune diseases that may recur, or a known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation;
Trial design
Treatments tested in this trial
- Tislelizumab
- Albumin-Bound Paclitaxel
- cis-platinum
- Surgery
- Radiation
- Nedaplatin
- Carboplatin