Docetaxol Plus Cisplatin Versus 5-Fu Plus Cisplatin as 1st-line Chemotherapy in Advanced ESCC Patients
Launched by SUN YAT-SEN UNIVERSITY · Dec 20, 2016
Trial Information
Current as of August 02, 2025
Unknown status
Keywords
ClinConnect Summary
Esophageal cancer is the 6th most common cause of cancer deaths worldwide and it is an endemic in many parts of the world, particularly in the developing countries, including China. Histologically, esophageal cancer can be classified as adenocarcinoma and esophageal squamous cell. carcinoma (ESCC) which is the most common histology in Asia. For locally advanced or metastatic ESCC patients, chemotherapy can improve overall survival (OS) and progression free survival (PFS). There is no standard first-line chemotherapy for ESCC patients. Cisplatin (DDP) plus fluorouracil is the most common use...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients must give written informed consent signed voluntarily by patients themselves or their supervisors witted by doctors.
- • 2. Patients must have histologically confirmed esophageal squamous cell carcinoma without prior treatments including surgery, chemotherapy, radiotherapy, and targeting treatment. Patients were allowed to have palliative radiotherapy 3 months before the enrollment and the target lesions should not be within the radiotherapy region. The last date of adjuvant therapy should be over 6 months before the enrollment.
- • 3. With measurable or evaluable disease according to the Response Evaluation Criteria in Solid Tumors (RECIST) criteria.
- • 4. With an expected life expectancy of ≥ 3 months.
- • 5. With a performance status of 0-1 on the Eastern Cooperative Oncology Group (ECOG) scale.
- • 6. Without serious system dysfunction and could tolerate chemotherapy.
- • 7. Patients must have normal bone marrow function with a hemoglobin (HGB) of ≥90g/L, an white blood cell (WBC) counts of ≥4.0×10\^9/L,a neutrophil count of ≥2.0×10\^9/L, , a platelet count of ≥100×10\^9/L.
- • 8. Patients must have normal liver and renal function with a total bilirubin (TBil) of ≤1.5 upper normal limitation (UNL), a creatinine (Cr) of ≤ 1.0 UNL, alanine aminotransferase (ALAT) and aspartate aminotransferase (ASAT) of ≤2.5 UNL.
- • 9. Patients must have normal electrocardiogram results and no history of congestive heart failure.
- • 10. Women of childbearing age should voluntarily take contraceptive measures. Without drug addition
- • 11. Patients must be with good compliance and agree to accept follow-up of disease progression and adverse events.
- Exclusion Criteria:
- • 1. Allergic to known drug
- • 2. Patients who have received prior treatment including chemotherapy, radiotherapy and surgery for the advanced or metastatic diseases.
- • 3. Receive docetaxel within 6 months as adjuvant or neoadjuvant chemotherapy.
- • 4. Brain metastasis.
- • 5. Without measurable or evaluable disease.
- • 6. With history of other tumors except for those of cervical carcinoma in situ or skin basal cell carcinoma who had been completely treated and without relapse in last 5 years.
- • 7. With serious diseases such as congestive heart failure, uncontrolled myocardial infarction and arrhythmia, liver failure and renal failure.
- • 8. With neurological or psychiatric abnormalities that affect cognitive.
- • 9. Pregnant or lactated women (premenopausal women must give urine pregnancy test before enrollment)
About Sun Yat Sen University
Sun Yat-sen University, a prestigious institution located in Guangzhou, China, is dedicated to advancing medical research and healthcare innovations. As a leading clinical trial sponsor, the university leverages its extensive academic resources and collaboration with top-tier medical professionals to conduct rigorous clinical studies. Committed to improving patient outcomes and contributing to global health knowledge, Sun Yat-sen University focuses on a wide range of therapeutic areas, employing cutting-edge methodologies to ensure the integrity and efficacy of its research initiatives. Through its clinical trials, the university aims to foster scientific advancements and enhance the quality of care provided to patients both locally and internationally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Guangzhou, Guangdong, China
Patients applied
Trial Officials
Rui-Hua Xu, MD, PhD
Principal Investigator
Sun Yat-sen University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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