About this trial
Immunotherapy combined with chemotherapy has become the standard first-line treatment regimen for gastric cancer. However, a subset of patients still fail to benefit or derive only limited benefit from this approach. This study aims to evaluate the addition of immunomodulatory EZH2 inhibitors or anti-angiogenic agents to the baseline regimen of immunotherapy combined with chemotherapy, in order to further improve patient treatment benefits.
Eligibility criteria
Qualifiers
Patients voluntarily agree to participate in this study and sign the informed consent form;
Age ≥ 18 years;
ECOG PS score 0-2;
Pathologically confirmed adenocarcinoma of the stomach/gastroesophageal junction;
Disqualifiers
Pregnant or lactating women;
Known HER2 positivity;
Patients with adverse events from previous treatments (except alopecia) that have not resolved to ≤ Grade 1 (CTCAE v5.0);
History of other malignant diseases within the past 5 years or concurrent malignant diseases, except for cured basal cell carcinoma of the skin and carcinoma in situ of the cervix;
Trial design
Treatments tested in this trial
- SHR1701
- SHR2554
- CAPOX
- Apatinib