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临床试验/NCT04521491
NCT04521491Unknown不适用

A Randomized Controlled Study on the Effect of Postoperative Adjuvant Chemotherapy With FOLFOX4 After Hepatocarcinoma Resection Based on Folate Receptor-positive Circulating Tumor Cells

Eastern Hepatobiliary Surgery Hospital1 个研究点 分布在 1 个国家目标入组 184 人开始时间: 2020年12月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
184
试验地点
1
主要终点
Recurrence free survival(RFS)

研究概览

简要总结

The aim of this study is to analyze the therapeutic effect of postoperative adjuvant chemotherapy with FOLFOX4 after hepatocarcinoma resection based on folate receptor-positive circulating tumor cells. Patients receiving curative resection (R0) were randomized to postoperative FOLFOX4 group and no FOLFOX4 group. The time to recurrence, the overall survival as well as the incidence of complications after therapy was observed to confirm the role of postoperative adjuvant therapy of FOLFOX4.

详细描述

Hepatocellular carcinoma (HCC) is the third leading cause of cancer death globally. Hepatectomy remains the most widely practiced radical treatment for HCC despite having a high associated recurrence rate, approximately 70% at 5 years after surgery, which often hampers further improvement in survival for these patients. And until now although a lot of different adjuvant therapies had been tried in the clinic, but their role in preventing recurrence remain controversial. As a research of a phase Ⅲ randomize study showed that FOLFOX4 (infusional fluorouracil [FU], leucovorin[LV], and OXA) served as palliative chemotherapy can induce higher overall survival, progression-free survival and response rate comparing to doxorubicin in patients with advanced hepatocellular carcinoma from Asia. The safety data was also acceptable. The chemotherapy of FOLFOX has been accepted by many guidelines and recommended for systematic treatment of advanced HCC. However, the effect of this systemic chemotherapy for recurrent HCC after partial hepatectomy remains to be investigated.

Circulating tumor cells (CTC) have played an important role in early diagnosis of tumors, monitoring of recurrence and metastasis, judgment of patient prognosis, and guidance of postoperative adjuvant treatment. CTC counts can be used to assist diagnosis and evaluation of postoperative prognosis. Previous studies have also shown that folate receptors (FR) are highly expressed in HCC. The detection of circulating tumor cells based on folate receptor (FR+CTC) has been proved to be a sensitive and effective method for detecting CTC.

Patients with HCC who received curative liver resection and with the preoperative FR+CTC level higher than 18.4FU/3mL were randomly assigned 1:1 by the doctors to receive placebo(control group) or FOLFOX4 (treatment group). All patients in the treatment group received FOLFOX4 at most 12 cycles beginning from the 4th week after liver resection. The outcomes of patients were evaluated during the 3-years follow up.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with HCC who received curative liver resection (R0);
  • Karnofsky Performance Score performance over 60;
  • The functions of the kidney, heart and lung and the blood system are normal and fittable for Licardin therapy;
  • The liver function is of grade A or B in Child-Pugh classification;
  • Patients agreed to collect peripheral blood for detection of CTC at the designated time point;
  • Patients should sign the informed consent of this study.

排除标准

  • If postoperative liver function is Child C, it cannot tolerate chemotherapy;
  • Blood transfusion history within 1 month before enrollment;
  • Severe gastroesophagealvarices with red sign or with variceal hemorrhage before;
  • Malignant or metastatic tumor in other sites in last 5 years;
  • Patients can not be followed-up regularly;
  • Patients participating in other trials or received other treatment previously.

研究组 & 干预措施

FOLFOX4

Experimental

Patients who will receive FOLFOX4 chemotherapy after liver resection

干预措施: FOLFOX4(infusional fluorouracil [FU], leucovorin [LV], and oxaliplatin [OXA]). (Drug)

结局指标

主要结局

Recurrence free survival(RFS)

时间窗: Up to 2 years

the time from randomization to documented progression

次要结局

  • Time to recurrence (TTR)(Up to 2 years)
  • Overall survival(OS)(Up to 2 years)

研究者

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

Shen Feng

MD

Eastern Hepatobiliary Surgery Hospital

研究点 (1)

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