drugset / Trial / NCT04799548

A Phase II Study of TACE Plus PD-1 Antibody in the Locally Advanced Stomach Adenocarcinoma

NCT04799548

Phase 2 Unknown 71 enrolled Shanghai Zhongshan Hospital
NaSingle-groupOpen-labelTreatment

Summary

This study is a phase II, prospective, single-center, single-arm trial to evaluate the efficacy and safety of the combination of neoadjuvant transcatheter arterial chemoembolization (TACE) and PD-1 antibody Tislelizumab in the locally advanced stomach adenocarcinoma. The primary purpose of this study is to evaluate the pathologic complete response (pCR) rate of TACE plus Tislelizumab. The second purpose is to evaluate pathologic response rate (pRR), objective Response Rate (ORR), overall survival (OS) and progression-free survival (PFS) of the patients enrolled in this study.

Timeline

Start
2021-12-30
Primary completion
2024-12
Completion
2026-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous
Background Oxaliplatin Small molecule 85 mg/m2 Other
Background Oxaliplatin Small molecule 130 mg/m2 Other
Background S-1 Small molecule 40 mg Oral
Background S-1 Small molecule 60 mg Oral

Indications