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Recruiting Phase 1, Phase 2 NCT05640609

Capeox Regimen Combined With Sintilimab and Bevacizumab for Gastric Cancer

Trial Parameters

Condition Stomach Neoplasm
Sponsor West China Hospital
Study Type INTERVENTIONAL
Phase Phase 1, Phase 2
Enrollment 57
Sex ALL
Min Age 18 Years
Max Age 70 Years
Start Date 2023-03-10
Completion 2024-11-01
Interventions
Capeox regimen combined with Sintilimab and Bevacizumab

Brief Summary

The median survival time of first-line chemotherapy for advanced gastric cancer is about one year, and the treatment is still facing the bottleneck. This is a one-arm, open and prospective phase II clinical study. Recruit patients who have been diagnosed with advanced or metastatic adenocarcinoma of the stomach and gastroesophageal junction and have not received systematic treatment.

Eligibility Criteria

Inclusion Criteria: 1. Histological or cytological diagnosis confirmed adenocarcinoma of stomach and gastroesophageal junction (including signet ring cell carcinoma, mucinous adenocarcinoma, hepatoid adenocarcinoma) 2. Imaging and surgical evaluation of unresectable recurrent or metastatic patients 3. The expected survival time was more than 3 months 4. The age is between 18 and 70 years old, both male and female 5. No systematic treatment has been given to patients with advanced or metastatic gastric and esophagogastric junction adenocarcinoma.If the patients who have received adjuvant or neoadjuvant therapy (including chemotherapy, radiotherapy and chemotherapy), the last treatment must be completed at least 6 months before randomization, and there is no recurrence or disease progression at the time of treatment.Palliative radiotherapy was allowed, but it must be completed at least 2 weeks before the first study treatment.Subjects were allowed to receive anti-tumor traditional Chines

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