Perioperative Treatment of Combined Radiotherapy With SOX, Apatinib and Camrelizumab for Oesophagogastric Cancer
- Sponsor
- Ruijin Hospital
- Study ID
- NCT07026149
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Gastric and Gastroesophageal Junction (GEJ) Adenocarcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Apatinib+Camrelizumab+SOX — DRUGApatinib 250mg+Camrelizumab 200mg +S-1, Oxaliplatin, q3w
- Preoperative Radiotherapy — RADIATIONRadiotherapy was administered using IMPT or IMRT. The target volume includes the gastric lesion, and regional lymph nodes. A regimen of 41.4 Gy in 23 fractions is preferred.
Study Details
The study is being conducted to evaluate the efficacy, safety and tolerability of radiotherapy and chemotherapy, apatinib with camrelizumab in the neoadjuvant (prior to surgery) and adjuvant (after surgery) treatment of previously untreated adults with gastric and gastroesophageal junction (GEJ) adenocarcinoma.
Key Dates
- Start date
- Jun 8, 2025
- Status verified
- Jun 2025
- Primary completion
- Sep 1, 2025
- Completion
- May 31, 2030
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm 1Radiotherapy and Apatinib and Camrelizumab and S-1 and Oxaliplatin
Primary Outcome Measure
Pathological Complete Response [ Time Frame: Up to 6 weeks after completion of radiotherapy and 3 cycles (each cycle is 21 days) of neoadjuvant drug treatment ]
Central Contacts
- Shu-Bei Wang, MD+86-021-64370045
- Gang Cai, MD+86-021-64370045
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