Neoadjuvant Immunotherapy and Chemoradiotherapy for Locally Advanced Esophagogastric Junction Adenocarcinoma

Inclusion Criteria: 1. Histologically confirmed adenocarcinoma of esophagogastric junction, and Her-2 negative. 2. Clinically diagnosed stage T3+orN+M0, according to CT/MRI scan. 3. No prior anti-tumor treatment, including surgery, chemotherapy, radiotherapy, and targeted therapy. 4. Eastern Cooperative Oncology Group(ECOG) performance status(PS) 0-1. 5. At least one evaluable lesion in abdominal CT/MRI according to RESIST 1.1 is required. 6. Expected survival ≥6 months. 7. Adequate organ function, Hemoglobin ≥90g/L; White blood cells ≥3.0×109/L; neutrophil count ≥1.5×109/L; Platelets ≥100×109/L; Serum creatinine (SCr) ≤ 1.5 times the upper limit of normal (ULN) or creatinine clearance rate ≥ 50ml/min (Cockcroft-Gault formula); Total bilirubin (TBIL) ≤ 1.5 times the ULN; Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) level ≤ 2.5 times the ULN; Urine protein \< 2+; if urine protein ≥ 2+, 24-hour urine protein quantification shows that protein must be ≤ 1 g. 8. Normal coagulation function, no active bleeding and thrombotic diseases: International Standardized Ratio INR≤1.5×ULN; Partial thromboplastin time APTT≤1.5×ULN; Prothrombin time PT≤1.5ULN; 9. Previous use of anti-tumor Chinese medicines, proprietary Chinese medicines, and immunomodulators (such as thymosin, interleukin, etc.) must be ≥ 2 weeks from the start of the study medication; 10. Female patients should not be pregnant or breast feeding. Male should contraception. 11. Able and willing to give informed consent to participate. 12. Those who are expected to have good compliance. Exclusion Criteria: 1. Existence of other active malignant tumors within 5 years or at the same time. 2. Already received chemotherapy, radiation therapy, targeted or immunotherapy. 3. Have any active autoimmune disease or history of autoimmune disease. 4. Patients with congenital or acquired immunodeficiency. 5. Use of immunosuppressive drugs within 14 days before the study start. 6. Administer live attenuated vaccines within 4 weeks before the study start. 7. Suffering from uncontrolled cardiac clinical symptoms or diseases, such as (1) NYHA II and above heart failure (2) unstable angina pectoris (3) myocardial infarction within 1 year (4) poorly controlled arrhythmia. 8. Patients with past and current interstitial pneumonia, pneumoconiosis, radiation pneumonia, drug-related pneumonia, etc., and severely impaired lung function. 9. Suffering from active pulmonary tuberculosis. 10. Complicated severe infection within 4 weeks before the the study start, or unexplained fever \>38.5°C during the screening period/before the study start. 11. Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation. 13\. Allergic to any drug in this study. 14. Combined with other severe, acute and chronic diseases that may increase the risk of participating. 15.Participators who had been recruited by other clinical trial within three months.