About this trial
The primary objective is to compare surgery with postoperative radiotherapy (PORT) versus surgery, in terms of the overall survival time (OS) in Stage II or III squamous cell esophageal carcinoma with neoadjuvant chemoradiotherapy(nCRT).
Eligibility criteria
Qualifiers
Patients must not have received any prior anticancer therapy Histologically-confirmed squamous cell carcinoma of the esophagus;
Tumors of the esophagus are located in the thoracic cavity;
Pre-treatment stageⅡ-Ⅲ (AJCC/UICC 8th Edition)
Male or non pregnant female
Disqualifiers
Patients with non-squamous cell carcinoma histology;
Patients with advanced inoperable or metastatic esophageal cancer;
Patients with another previous or current malignant disease;
Any patient with a significant medical condition which is thought unlikely to tolerate the therapies. Such as cardiac disease;
Trial design
Treatments tested in this trial
- Neoadjuvant Radiotherapy Program:
- Neoadjuvant chemotherapy Program
- Esophagectomy program:
- Postoperative radiotherapy program