RecruitingPhase 2NCT05515315

Induction Tislelizumab Combined With Chemotherapy Followed by Definitive Chemoradiotherapy in the Treatment of Locally Unresectable Esophageal Squamous Cell Carcinoma


Sponsor

Fuzhou General Hospital

Enrollment

93 participants

Start Date

May 31, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

To explore the efficacy of Tislelizumab combined with chemotherapy in the treatment of locally unresectable esophageal squamous cell carcinoma (ESCC)


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether adding tislelizumab (an immunotherapy drug) to standard chemotherapy before definitive chemoradiation improves outcomes for patients with locally advanced esophageal squamous cell carcinoma (ESCC) that cannot be surgically removed. This approach — induction therapy followed by definitive concurrent chemoradiotherapy — aims to shrink the tumor first, then eliminate it with combined treatment. **You may be eligible if...** - You are between 18 and 70 years old - You have confirmed ESCC at stage II–IVA that is inoperable (either medically unfit for surgery or choosing non-surgical treatment) - You have not received prior treatment for esophageal cancer - Your ECOG performance score is 0 or 1 (able to care for yourself) - Your blood counts and organ function meet the study requirements **You may NOT be eligible if...** - Your cancer has spread to distant organs - You have had prior treatment for esophageal cancer - You have an active autoimmune disease - You are taking long-term steroids or immune-suppressing medications - You are pregnant or breastfeeding 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.

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Interventions

DRUGTislelizumab

Participants will receive Tislelizumab, 200mg, intravenously over 30 - 60 minutes, day 1 of every 3 weeks

DRUGAlbumin paclitaxel

Participants will receive Albumin paclitaxel 260 mg/m2 , day 1 of every 3 weeks

DRUGNedaplatin

Participants will receive Nedaplatin 80 mg/m2 , day 1 of every 3 weeks

RADIATIONradiotherapy

50-60Gy/25-30f


Locations(1)

Ye zai sheng

Fuzhou, Fujian, China

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NCT05515315