RecruitingPhase 2NCT07067268

Tislelizumab Combined With Capecitabine for Nasopharyngeal Carcinoma With Residual EBV DNA After Radiotherapy

A Multicenter, Randomized Controlled, Phase II Trail of Tislelizumab Combined With Capecitabine for Nasopharyngeal Carcinoma Patients With Residual Epstein-Barr Virus (EBV) DNA After Radiotherapy


Sponsor

Fudan University

Enrollment

76 participants

Start Date

Sep 14, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to explore the efficacy and safety of tislelizumab combined with capecitabine in nasopharyngeal carcinoma patients with residual plasma EBV DNA after radiotherapy.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adding an immunotherapy drug (tislelizumab) and an oral chemotherapy (capecitabine) can eliminate residual cancer in people with nasopharyngeal carcinoma (a type of cancer at the back of the nose and throat) who still have detectable Epstein-Barr virus (EBV) DNA in their blood after completing radiation therapy. **You may be eligible if...** - You are 18 or older with a confirmed diagnosis of nasopharyngeal carcinoma - You have already completed radiation therapy (with or without chemotherapy) - After radiation, your blood still shows detectable EBV DNA - Your blood counts, liver, kidney, and heart function are in adequate range **You may NOT be eligible if...** - You have a specific cancer subtype called keratinizing squamous cell carcinoma (WHO type I) - Your cancer has spread to distant parts of the body - You have active autoimmune disease, active tuberculosis, hepatitis B or C, or HIV - You have significant heart disease - You are pregnant or unwilling to use contraception Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGAdjuvant therapy

Tislelizumab: 200 mg IV on day 1, every 3 weeks Capecitabine: 1000 mg/m² orally twice daily on days 1-14,every 3 weeks Treatment duration: 8 cycles


Locations(1)

Fudan Universtiy Shanghai Cancer Centre

Shanghai, China, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07067268


Related Trials