Sintilimab Combined With LDRT for Neoadjuvant Treatment of Locally Advanced dMMR/MSI-H Gastric Cancer

Prior treatment

• Undergoing other drug clinical trials or having participated in any drug clinical trials one month before enrollment.
• Receiving corticosteroids (\> 10mg/d prednisone or equivalent dose of steroids) or other systematic immunosuppression therapies within 14 days before enrollment, excluding the following therapies: steroid hormone replacement therapy (≤10mg/d); local steroid therapy; and short-term, prophylactic steroid therapy for preventing allergies or nausea and vomiting.
• Active or clinically significant cardiac disease:
  • Congestive heart failure \> New York Heart Association (NYHA) class 2;
  • Active coronary artery disease;
  • Arrhythmias requiring treatment other than β-blockers or digoxin;
  • Unstable angina (with angina symptoms at rest), new angina within 3 months before enrollment, or new myocardial infarction within 6 months before enrollment
• Epileptic that needs medication.
• Other antitumor therapy (chemotherapy, radiotherapy, surgery, immunotherapy, biotherapy, chemoembolization) other than investigator drugs. Palliative external irradiation for non-target lesions is allowed.
• Previously used similar immune checkpoint inhibitors.
• Major surgery 4 weeks before recruitment, open biopsy or major trauma surgery (excluding biliary stents, or percutaneous biliary drainage).
• Treatment with antitumor Chinese herbal medicine.

Other illness

• Active autoimmune disease or history of refractory autoimmune disease.
• Other tumors that have not been treated or exist at the same time, except carcinoma in situ of the cervix, treated basal cell carcinoma or superficial bladder tumor. If the tumor was cured and no evidence of disease was found for more than 3 years, the patient can be enrolled. All other tumors must be treated at least 3 years before enrollment.
• Patients with a history of HIV infection or active hepatitis B/C.
• Ongoing \> level 2 infection.
• Renal failure patients requiring blood or peritoneal dialysis.
• History of organ transplantation (including corneal transplantation).
• Allergic to research drugs or similar drugs, or suspected allergies.
• Medical, psychological or social conditions can affect the recruitment of patients and evaluation of study results.

Other

• Unable to comply with the research program or procedures.
• Symptomatic brain metastasis or meningioma.
• Unhealed wounds, ulcers or fractures.
• Active, symptomatic interstitial pneumonia, pleural or ascites that causes dyspnea (dyspnea ≥ 2 grade).
• Pregnant or lactating women.
• The investigator believes that patients who are not suitable for the study.

• Age 18-80 years.
• Histologically or cytologically confirmed diagnosis of locally advanced G/GEJ adenocarcinoma (cT2N+M0 or cT3-4aNanyM0) as assessed by exploratory laparoscopic surgery, ultrasonography and/or CT/MRI.
• Resectable G/GEJ cancer, as judged by experienced surgeons.
• dMMR and/or MSI-H.
  • 4\. Eastern Cooperative Oncology Group performance score (ECOG PS) ≤1. 5. Agree to provide blood, feces, and tissue specimens. 6. The expected survival is longer than 6 months. 7. There was no previous antitumor treatment (including chemotherapy, radiotherapy, targeted therapy, immunotherapy, interventional therapy, and other treatments with antitumor effects).
  • 8\. Adequate organ and hematological function. 9. Strict contraception. 10. Patients must be able to understand and be willing to sign the written informed consent form. A signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure.