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临床试验/NCT01972490
NCT01972490已完成4 期

Study of Avastin in Combination With Chemotherapy for the First Line Treatment of RAS Mutant Unresectable Colorectal Liver-limited Metastases

Xu jianmin1 个研究点 分布在 1 个国家目标入组 241 人开始时间: 2013年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
241
试验地点
1
主要终点
the rate of patients converted to resection for liver metastases

研究概览

简要总结

In this study, the investigators assessed the effect of avastin in combination with chemotherapy in the treatment of RAS mutant-type, unresectable colorectal liver-limited metastases

详细描述

Patients will be eligible for inclusion if the patients have histologically confirmed colorectal adenocarcinoma with RAS mutant liver-confined metastases deemed non-resectable. Eligible patients will be randomly assigned to chemotherapy plus avastin (arm A) or chemotherapy alone (arm B). Treatment will continue until tumor response indicates suitability for surgery for liver metastases or until disease progression or unacceptable toxic effects. The primary endpoint is the conversion rate to radical resection for liver metastases,which will be assessed by local multidisciplinary team (includes more than three liver surgeons and one radiologist) with the use of contrast-enhanced CT or MRI after 4 cycles and then every other 4 cycles up to 12 cycles. To provide an objective assessment of changes in resectability, radiological images will be presented by a radiologist to more than 3 liver surgeons, who are blinded to the clinical data. Patients will be considered resectable if 50% or more of surgeons vote for radical resection of LM. For patients whose liver-metastases are assessed resectable, resection should be scheduled to be performed within 2~3 weeks of the last treatment cycle. Following resection, patients will be advised to continue the same therapeutic regimen until the treatments reach a sum of 12 cycles.

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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 and ≤ 75 years;
  • Primary tumour was histologically confirmed colorectal adenocarcinoma;
  • Together with clinical or radiological evidence of first occurrence of non-resectable liver-only metastases
  • With evidence of tumor RAS gene mutant status;
  • With at least one measurable tumor.
  • Performance status (ECOG) 0~1
  • A life expectancy of ≥ 3 months
  • Adequate hematological function: Neutrophils≥1.5 x109/l and platelet count≥100 x109/l; Hb ≥9g/dl (within 1 week prior to randomization)
  • Adequate hepatic and renal function: Serum bilirubin≤1.5 x upper limit of normal (ULN), alkaline phosphatase ≤5x ULN, and serum transaminase (either AST or ALT) ≤ 5 x ULN(within 1 week prior to randomization);
  • Written informed consent for participation in the trial.

排除标准

  • Previous exposure to target therapy, chemotherapy, radiotherapy or intervention therapy for colorectal liver metastases.
  • Known or suspected extrahepatic metastases.
  • Patients with known hypersensitivity reactions to any of the components of the study treatments.
  • Having previously participated in a study which included a possibility of being allocated to avastin therapy (whether or not the patient actually received avastin)
  • Clinically relevant coronary artery disease or a history of a myocardial infarction within the last 12 months or left ventricular ejection fraction (LVEF) below the institutional range of normal
  • Acute or sub-acute intestinal occlusion
  • Pregnancy (absence confirmed by serum/urine β-HCG) or breast-feeding
  • Other previous malignancy within 5 years, with exception of a history of a previous basal cell carcinoma of the skin or pre-invasive carcinoma of the cervix
  • Known drug abuse/ alcohol abuse
  • Legal incapacity or limited legal capacity
  • Pre-existing peripheral neuropathy.

研究组 & 干预措施

ARM A

Experimental

patients received avastin in combination with mFOLFOX6

干预措施: avastin (Drug)

ARM A

Experimental

patients received avastin in combination with mFOLFOX6

干预措施: mFOLFOX6 (Drug)

ARM B

Active Comparator

Patients received mFOLFOX6 alone

干预措施: mFOLFOX6 (Drug)

结局指标

主要结局

the rate of patients converted to resection for liver metastases

时间窗: 3 years

To explore whether avastin in combination with chemotherapy as treatment could improve the resection rate in patients with RAS mutant-type, unresectable colorectal liver-limited metastases compared with chemotherapy alone.

次要结局

  • progression free survival(3 years)
  • tumor response(3 years)
  • overall survival(3 years)

研究者

发起方
Xu jianmin
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Xu jianmin

Jianmin Xu, PhD Fudan University

Fudan University

研究点 (1)

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