About this trial
Esophageal cancer is one of the most common malignancies in China, and esophageal squamous cell carcinoma (ESCC) is the predominant histological type. Surgical resection is still a standard therapeutic approach for patients with resectable ESCC, but the prognosis is still disappointing. Although neoadjuvant chemoradiotherapy plus surgery is currently recommended for patients with locally advanced ESCC, it is still an infrequently used procedure in China. The efficacy of adjuvant therapy on ESCC is still controversial. Recently, the CheckMate 577 trial showed that adjuvant nivolumab therapy could improve DFS for patients with residual disease after neoadjuvant chemoradiotherapy plus surgery. However, no optimal postoperative adjuvant therapy was recommended for patients with ESCC received upfront surgery. We designed a prospective randomized controlled tial to study whether immunotherapy could be used with chemotherapy after surgery to improve overall survival in these patients. The primary endpoint of the study is disease free survival, with secondary endpoints of overall survival, safety and toxicity, and quality of life.
Eligibility criteria
Qualifiers
Aged between 18 and 70 years
Untreated before surgery (e.g. radiotherapy, chemotherapy, target therapy and immunotherapy)
Histologically documented squamous cell carcinoma of the thoracic esophagus with positive lymph nodes (T1-3N1-3M0)
undergoing radical esophagectomy
Disqualifiers
previous or concurrent malignancy
Interstitial lung disease
Requiring systemic treatment with either corticosteroids or other immunosuppressive medications
Known or suspected allergy to chemotherapeutic drugs or Tislelizumab
Trial design
Treatments tested in this trial
- Tislelizumab