Concurrent Chemoradiotherapy Combined With Sintilimab as Neoadjuvant Therapy for Advanced Gastric Cancer Patients With Para-aortic Lymph Node Metastasis: a Single-arm, Phase II, Exploratory Study.
Overview
- Phase
- Phase 2
- Intervention
- Sintilimab
- Conditions
- Gastric Cancer
- Sponsor
- The First Affiliated Hospital with Nanjing Medical University
- Enrollment
- 40
- Locations
- 1
- Primary Endpoint
- Recurrence free survival (RFS)
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
This trial is a prospective, single arm, single center, phase II clinical study aimed at subjects with advanced gastric cancer and para aortic lymph node metastasis, exploring the feasibility and safety of Sintilimab Injection combined with synchronous chemo-radiotherapy as neoadjuvant therapy.
Patients will receive sintilimab Injection (200mg iv q3w d1) combined with concurrent radiotherapy and chemotherapy. The chemotherapy regimen will use oxaliplatin 130mg/m2+S-1 40mg/m2 bid d1-14. Radiotherapy is performed using intraperitoneal radiation therapy, once a day, five times a week, at a dose of 1.8-2 Gy/f, for a total of 45-50.4 Gy (60-66 Gy for lymph node lesions). Radiation therapy starts from the second cycle of Sintilimab Injection combined with chemotherapy. The subjects underwent imaging evaluation after completing 4 cycles of combination chemotherapy and radiation therapy with Sintilimab Injection. Evaluated as a surgical subject (surgical conditions: imaging evaluation of enlarged lymph nodes adjacent to the abdominal aorta with PR or no significant activity), radical surgery will be performed within 4 weeks after the last study drug treatment. After surgery, the researcher will determine the necessity of adjuvant treatment and develop an adjuvant treatment plan based on the subject's condition. Subjects evaluated as inoperable will have their best follow-up treatment plan determined by the researcher.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Arms & Interventions
combination therapy
sintilimab combined with chemotherapy and radiotherapy
Intervention: Sintilimab
combination therapy
sintilimab combined with chemotherapy and radiotherapy
Intervention: Extraperitoneal radiation therapy
combination therapy
sintilimab combined with chemotherapy and radiotherapy
Intervention: Oxaliplatin
combination therapy
sintilimab combined with chemotherapy and radiotherapy
Intervention: S-1
Outcomes
Primary Outcomes
Recurrence free survival (RFS)
Time Frame: 24 months
Recurrence free survival of patients undergoing surgery after Sintilimab Injection combined with concurrent chemoradiotherapy
Secondary Outcomes
- Adverse reactions(24 months)
- Overall survival (OS)(24 months)
- R0 resection rate(12 months)
- Major pathological response rate (MPR)(12 months)
- Objective response rate (ORR)(24 months)