Actively Recruiting
Surgery or Chemoradiotherapy for Cervical Esophageal Cancer
Led by Cancer Institute and Hospital, Chinese Academy of Medical Sciences · Updated on 2022-04-14
192
Participants Needed
1
Research Sites
351 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To compare surgery with definitive chemoradiotherapy for patients with resectable cervical esophageal squamous cell carcinoma.
CONDITIONS
Official Title
Surgery or Chemoradiotherapy for Cervical Esophageal Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with resectable cervical esophageal squamous cell carcinoma (cT1b-T4aN0-3M0)
- Cervical esophageal cancer spreading to the hypopharynx or thoracic esophagus can be included
- Aged between 18 and 75 years
- No contraindications for surgery
- Hemoglobin level at least 90 g/L
- Leukocyte count at least 4.0 x 10^9/L
- Absolute neutrophil count at least 1.5 x 10^9/L
- Platelet count at least 100 x 10^9/L
- Total bilirubin no higher than 1.5 times the upper limit of normal (ULN)
- ALT no higher than 2.5 times ULN
- AST no higher than 2.5 times ULN
- Serum creatinine no higher than 1.5 times ULN or creatinine clearance rate at least 50 mL/min
- INR no higher than 1.5 times ULN
- APTT no higher than 1.5 times ULN
- No other malignancies
- Expected complete tumor removal (R0 resection)
- ECOG performance status 0 or 1
- Willingness to participate and signed informed consent form
You will not qualify if you...
- Presence of other malignancies
- Mental health disorders
- Hemorrhagic diseases
- Patients who cannot undergo surgery
- Pregnant or lactating women
- Allergic history to paclitaxel or cisplatin
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cancer Hospital Chinese Academy of Medical Sciences
Beijing, China
Actively Recruiting
Research Team
Z
Zhen Wang, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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