Actively Recruiting

Phase 2
Age: 18Years - 75Years
All Genders
NCT06463834

A Study of Sintilimab Combined With Chemotherapy for Neoadjuvant Treatment of Esophageal Squamous Cell Carcinoma

Led by Fujian Cancer Hospital · Updated on 2024-06-18

30

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is aimed to evaluate the efficacy and safety of sintilimab combined with chemotherapy (docetaxel+cisplatin+5-fluorouracil, DCF) in neoadjuvant treatment of locally advanced esophageal squamous cell carcinoma.

CONDITIONS

Official Title

A Study of Sintilimab Combined With Chemotherapy for Neoadjuvant Treatment of Esophageal Squamous Cell Carcinoma

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 75 years
  • Diagnosis of esophageal squamous cell carcinoma confirmed by biopsy
  • Primary tumor located in the middle of the esophagus with stage T1b-3N1-3M0/M1 or T3N0M0 by CT/MRI/EUS (AJCC 8th edition)
  • At least one measurable lesion
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1
  • Adequate organ function
Not Eligible

You will not qualify if you...

  • Active cancer within the past 5 years other than the study tumor or cured localized tumors like resected basal or squamous cell carcinoma, superficial bladder cancer, cervical carcinoma in situ, or breast cancer
  • High risk of bleeding or perforation due to tumor invasion of adjacent organs such as the aorta or trachea, or presence of fistula
  • Prior anti-tumor therapy for the esophageal cancer, including radiotherapy, chemotherapy, immunotherapy, or traditional Chinese medicine therapy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Fujian Cancer Hospital

Fuzhou, Fujian, China, 350014

Actively Recruiting

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Research Team

S

Shuoyan Liu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

0

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