Perioperative Surufatinib Plus Sintilimab Combined With Chemotherapy in Gastric/Gastroesophageal Junction Adenocarcinoma

The incidence of gastric and gastroesophageal junction adenocarcinoma is increasing in China, and it is one of the most common malignant tumors in China. Surgery is the only possible way to cure gastric and gastroesophageal junction adenocarcinoma, however, over 70-80% of gastric/gastroesophageal junction adenocarcinoma patients in China are in advanced stage. Locally gastric/gastroesophageal junction adenocarcinoma (cT3-4bNanyM0) could be cured by multi-disciplinary therapies including surgery, immunotherapy and chemotherapy. Perioperative immunotherapy plus chemotherapy can downstage tumor T and N stage, increase the R0 resection rate, and may improve the long-term survival. However, the therapeutic effects still not satisfactory to date. Surufatinib, as the novel oral antivascular targeting drug, has been proved to be effective in neuroendocrine tumor. Combination of perioperative surufatinib and immunotherapy plus chemotherapy for locally advanced gastric/gastroesophageal junction adenocarcinoma could be a novel therapeutic strategy to increase response rate and therapeutic efficacy. This study is a monocenter, single-arm phase 2 clinical trial to evaluate tolerability, safety and efficacy of perioperative surufatinib in combination with sintilimab and chemotherapy in locally advanced gastric and gastroesophageal junction adenocarcinoma.

Inclusion criteria

• signed informed consent
• patients age 18-75 years;
• Histologically CT/MRI confirmed cT3-4bNanyM0 gastric or GEJ adenocarcinoma;
• ECOG 0-1, no surgery contraindications;
• Expected survival ≥3 months;

Exclusion criteria

• signs of distant metastases
• Prior chemotherapy, radiotherapy, surgery for gastric cancer;
• Significant cardiovascular disease
• major surgical procedure within 4 weeks prior to initiation of study treatment
• current treatment with anti-viral therapy or HBV
• pregnancy or breastfeeding
• history of malignancy within 5 years prior to screening
• Present or history of any autoimmune disease or immune deficiency;
• Prior therapy with a PD-1, anti-PD-Ligand 1 (PD-L1) or CTLA-4 agent;
• There are active gastric and duodenal ulcers, ulcerative colitis and other gastrointestinal diseases, or active bleeding in unresectable tumors.
• Poorly controlled hypertension or diabetes;