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Study identifier: NCT07549100 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Efficacy and Safety of Tislelizumab Plus Chemotherapy as Conversion Therapy in Unresectable Locally Advanced ESCC

Condition: Locally Advanced Esophageal Squamous Cell Carcinoma  ·  Sponsor: Shandong Provincial Hospital

PhaseN/A
Planned participants30
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This is a single-arm, single-center, open-label, observational clinical study. A total of 30 patients with initially unresectable locally advanced esophageal squamous cell carcinoma will be enrolled.Eligible patients will receive albumin-bound paclitaxel (260 mg/m², day 1, every 3 weeks \[Q3W\]) plus cisplatin (75 mg/m²) or carboplatin (AUC = 5), in combination with tislelizumab (200 mg, day 2, Q3W), for 2-4 cycles. Tumor staging will be reassessed thereafter, and the feasibility of surgical resection will be determined based on multidisciplinary team (MDT) discussion.The primary endpoint is the conversion rate to surgery. Secondary endpoints include pathological complete response (pCR), objective response rate (ORR), and safety.

This description comes directly from the study's public registry record.

Talk to the study team

ALei Feng  ·  +8613402214659  ·  370100668@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Shandong Provincial HospitalJinan, Shandong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07549100