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临床试验/NCT03365765
NCT03365765已完成3 期

Exploratory Study on the Efficacy and the Safety of mFOLFOX6 Chemotherapy With Apatinib as Postoperative Treatment in Stage IIIB or IIIC Colorectal Cancer

Huashan Hospital1 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2018年2月12日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
63
试验地点
1
主要终点
disease-free survival

研究概览

简要总结

This study will focus on postoperative patients of stage IIIB or stage IIIC colorectal cancer. These patients will start to accept chemotherapy in 3-4 weeks after operation, these patients were randomly divided into two groups, one group will accept adjuvant chemotherapy of mFOLFOX6; another group will use mFOLFOX6 combined with apatinib. The efficacy and safety of adjuvant chemotherapy will be compared between the two groups. Disease-free survival, overall survival, incidence of adverse reaction of chemotherapy and postoperative quality of life will be recorded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • signed informed consent form;
  • confirmed as colorectal cancer by pathology, and the stage is IIIB /IIIC according to the NCCN guidelines;
  • patients with primary colorectal cancer;
  • radical resection of colon cancer (CME) or radical resection of rectal cancer (TME) has done;
  • 3~4 weeks after radical resection ;
  • patients did not receive any radiotherapy and chemotherapy before operation

排除标准

  • emergency operation for colorectal cancer patients;
  • the situation after operation can not tolerance for systemic adjuvant chemotherapy (hemoglobin <95g/L, white blood cell <3 * 109/L, granulocyte <1.5 * 109/L and platelet <75 * 109/L, bilirubin>2.5N, alanine aminotransferase >2.5N, alkaline phosphatase >2.5N, urea nitrogen >2.5N, creatinine >2.5N, proteinuria, hematuria, temperature of >38 degree);
  • serious diseases such as cardiac insufficiency, respiratory insufficiency, liver and kidney dysfunction, serious blood diseases;
  • patients participated in other clinical trials at the same time;
  • pregnant or perinatal women;
  • combined with other malignant tumors;
  • a history of neuropsychiatric disorders;
  • patients have used anti angiogenesis targeted drugs (such as bevacizumab, cetuximab);
  • patients had a history of severe trauma within 4 weeks before admission;
  • allergic to chemotherapy drugs or apatinib;
  • active bleeding, ulcers, intestinal perforation, intestinal obstruction, hypertension

研究组 & 干预措施

mFOLFOX6 & apatinib

Experimental

oxaliplatin 85mg/m2 intravenous infusion for 2 hours, intravenous infusion of leucovorin 400mg/m2 for 2 hours, intravenous infusion of 5- fluorouracil 400mg/m2, first days; 5- fluorouracil 2400mg/m2 continuous intravenous infusion for 46-48 hours, repeated 1 time every two weeks, a total of 12 cycles, 24 weeks. Patients also take apatinib, 1 time daily, 500mg each time, lasting 1 year, from the first chemotherapy of mFOLFOX6.

干预措施: Apatinib (Drug)

mFOLFOX6 & apatinib

Experimental

oxaliplatin 85mg/m2 intravenous infusion for 2 hours, intravenous infusion of leucovorin 400mg/m2 for 2 hours, intravenous infusion of 5- fluorouracil 400mg/m2, first days; 5- fluorouracil 2400mg/m2 continuous intravenous infusion for 46-48 hours, repeated 1 time every two weeks, a total of 12 cycles, 24 weeks. Patients also take apatinib, 1 time daily, 500mg each time, lasting 1 year, from the first chemotherapy of mFOLFOX6.

干预措施: Oxaliplatin (Drug)

mFOLFOX6 & apatinib

Experimental

oxaliplatin 85mg/m2 intravenous infusion for 2 hours, intravenous infusion of leucovorin 400mg/m2 for 2 hours, intravenous infusion of 5- fluorouracil 400mg/m2, first days; 5- fluorouracil 2400mg/m2 continuous intravenous infusion for 46-48 hours, repeated 1 time every two weeks, a total of 12 cycles, 24 weeks. Patients also take apatinib, 1 time daily, 500mg each time, lasting 1 year, from the first chemotherapy of mFOLFOX6.

干预措施: 5-fluorouracil (Drug)

mFOLFOX6

Active Comparator

oxaliplatin 85mg/m2 intravenous infusion for 2 hours, intravenous infusion of leucovorin 400mg/m2 for 2 hours, intravenous infusion of 5- fluorouracil 400mg/m2, first days; 5- fluorouracil 2400mg/m2 continuous intravenous infusion for 46-48 hours, repeated 1 time every two weeks, a total of 12 cycles, 24 weeks.

干预措施: Oxaliplatin (Drug)

mFOLFOX6

Active Comparator

oxaliplatin 85mg/m2 intravenous infusion for 2 hours, intravenous infusion of leucovorin 400mg/m2 for 2 hours, intravenous infusion of 5- fluorouracil 400mg/m2, first days; 5- fluorouracil 2400mg/m2 continuous intravenous infusion for 46-48 hours, repeated 1 time every two weeks, a total of 12 cycles, 24 weeks.

干预措施: 5-fluorouracil (Drug)

结局指标

主要结局

disease-free survival

时间窗: 5 years

observe the recurrence of colorectal cancer after operation

次要结局

  • incidence of adverse reactions after chemotherapy(one year)
  • overall survival(5 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jianbin Xiang

professor

Huashan Hospital

研究点 (1)

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