The purpose of this study is to evaluate the efficacy and safety of \*\*Disitamab Vedotin combined with Tislelizumab and CAPOX versus Tislelizumab combined with CAPOX\*\* as first-line treatment for patients with HER2-low advanced gastric or gastroesophageal junction adenocarcinoma.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
616
Disitamab Vedotin: 2.5 mg/kg, IV, D1, Q2W; Tislelizumab: 200 mg, IV, D1, Q3W Oxaliplatin: 100 mg/m², IV, D1, Q3W; Capecitabine: 750 mg/m², po, BID, D1-D14, Q3W
Tislelizumab: 200 mg, IV, D1, Q3W Oxaliplatin: 130 mg/m², IV, D1, Q3W; Capecitabine: 1000 mg/m², po, BID, D1-D14, Q3W
Beijing Cancer Hospital
Beijing, BJ-Beijing, China
Progression-Free Survival
Time frame: 24 months
Overall Survival
Time frame: up to 5 years
Objective Response Rate
Time frame: 24 months
Disease Control Rate
Time frame: 24 months
Duration of Response
Time frame: 24 months
Patient-Reported Outcomes
Time frame: 24 months
Adverse Events
Time frame: 24 months
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