This is a single-center, retrospective clinical study to evaluate the efficacy and safety of tislelizumab combined with first-line chemotherapy in the treatment of HER2-negative advanced gastric cancer.
This study aims to include 60 HER-2 negative advanced gastric cancer patients who received first-line treatment with tislelizumab combined with chemotherapy in our hospital from November 1, 2020 to November 1, 2021. Clinicopathological data, blood tests and imaging data of the patients were collected. The primary endpoints evaluated were PFS and OS, and the secondary endpoints were ORR and safety. At the same time, ctDNA and peripheral cytokine status of patients as well as second-generation sequencing of tumor tissues at baseline were collected for the exploration of therapeutic efficacy related biomarkers.
Study Type
OBSERVATIONAL
Enrollment
60
Tislelizumab:200mg, iv, d1, 21 days per cycle, until disease progression or intolerable toxicity
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Beijing, China
PFS
Progression-free Survival
Time frame: 2 years
OS
Overall Survival
Time frame: 3 years
ORR
Objective Remission Rate
Time frame: 2 years
DCR
Disease Control Rate
Time frame: 2 years
DOR
Duration of Remission
Time frame: 2 years
Safety and Tolerability
Incidence of Treatment-Emergent Adverse Events
Time frame: 2 years
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