A three-arm Phase III trial was started in Oct. 2014. Definitive chemoradiotherapy with cisplatin plus 5-fluorouracil is the standard in Western countries in esophagus cancer. But in China because of its toxic reaction, most of patients stop the halfway. Because low toxicity, the chemotherapy regimen of capecitabine with or without oxaliplatin are widely used in clinical. The purpose of this study is to confirm the difference of Capecitabine plus with or without oxaliplatin over cisplatin plus 5-fluorouracil with definitive chemoradiotherapy for esophagus squamous cell carcinoma. A total of 249 patients will be accrued from China within 2 years. The primary endpoints are grade 3-5 AEs and overall survival and the secondary endpoints include progression-free survival, response rate, pathologic complete response rate.
We plan to recruit the patients who were pathologically confirmed with esophageal squamous cell carcinoma from the Oct 2014. The patients will be divided into three groups.Experimental group 1 : single drug Capecitabine and concurrent radiotherapy.Experimental group 2: Capecitabine plus oxaliplatin and concurrent radiotherapy. Control group:cisplatin plus 5-fluorouracil and concurrent radiotherapy. To evaluate the adverse events and the overall survival of the three group. Also observe the patient's progression-free survival, response rate, pathologic complete response rate.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
249
capecitabine(Aibin):625mg/m2, bid d1-5; q1w, po,5 weeks in total
Oxaliplatin(Aiheng):65mg/m2,d1,8, 22, 29,I.V.
concurrent radiotherapy: 50Gy in total,2 Gy/d,5d/w,Until disease progression or unacceptable toxicity
The First Affiliated Hospital of Henan University of Science and Technology
Luoyang, Henan, China
Grade 3/5 acute toxicities
Grade 3/5 acute toxicities occurred during or within 90 days after RT
Time frame: 90 days
OS-2 year
Overall Survival rate in 2 year from Randomization
Time frame: 2 years
PFS-2 year
Progression Free Survival rate in 2 year from Randomization
Time frame: 2 years
overall remission rate, ORR
overall remission rate after CRT
Time frame: 16 weeks
quality of life, Qol
quality of life evaluation
Time frame: 16 weeks
pathologic complete response rate
pathologic complete response rate confirmed by gastroscope biopsy
Time frame: 16 weeks
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