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Clinical Trial Summary

To evaluate the efficacy of metronomic chemotherapy combination with tislelizumab in EGFR/ALK-negative advanced NSCLC patients intolerant to first-line standard chemotherapy.


Clinical Trial Description

This study is a clinical intervention study. The patients who comfirm the criteria will be treated with tislelizumab plus metronomic oral vinorelbine. The patients will be followed up until the tumor progressed, and the efficacy (PFS, ORR, DCR) of tumor therapy were evaluated. Drug administration regimen: tislelizumab 200mg intravenous drip once every 3 week3; Oral Vinorelbine 40mg three times a week for three weeks and Q28d for one course. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06260553
Study type Interventional
Source Fujian Cancer Hospital
Contact
Status Enrolling by invitation
Phase Phase 2
Start date February 7, 2024
Completion date August 7, 2025