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临床试验/NCT03401294
NCT03401294招募中2 期

Conversion From Unresectable To Resectable Liver Metastases In Patients With Liver-Only Metastatic Colorectal Cancer Treated With FOLFOXIRI Plus Bevacizumab. The Conversion Trial.

University of Saskatchewan1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2025年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
32
试验地点
1
主要终点
Rate of liver metastasectomy

研究概览

简要总结

Most patients with mCRC are treated with palliative chemotherapy and only a small number of patients with limited metastatic disease achieve long-term remission following metastasectomy. There is a growing need for more effective treatment in patients with liver-only mCRC to improve the rate of curative resection without compromising QOL.The current study is informed by our patient's needs. It aims to evaluate the rate of conversion therapy in patients with unresectable liver-only mCRC using the combination of FOLFOXIRI and bevacizumab and to assess the association between an early FDG-PT/CT response and other clinical and pathological biomarkers and hepatic metastasectomy.

详细描述

Colorectal cancer is the second leading cause of cancer-related death in North America. Patients with metastatic colorectal cancer generally have limited life expectancy, however, a small number of patients with liver-only metastases could potentially be cured following surgical resection of metastases. Patients and their family strongly feel that there is an unmet need for a more effective treatment in metastatic colorectal cancer to improve disease response rate and thereby curative surgery. Recent evidence suggest that a triplet chemotherapy regimen, FOLFOXIRI plus bevacizumab has been associated with higher response rates. The CONVERSION trial will evaluate the rate of conversion from unresectable to resectable liver metastases in patients with liver-only metastatic colorectal cancer treated with FOLFOXIRI-bevacizumab. Furthermore, this study will assess disease control rate, survival, quality of life and association between various biomarkers including an early FDG-PET/CT response and curative surgery. Thirty-two eligible patients will be recruited at the two major cancer centers in Saskatchewan. Patients will receive FOLFOXIRI-bevacizumab every two weeks for a total of 12 cycles and will undergo periodic imaging studies. The resectability of liver metastases will be assessed by a multidisciplinary team comprised of surgeons, radiologists, and oncologists. This study will be helpful to establish a standard chemotherapy regimen for patients with liver-only metastatic colorectal cancer and to determine the role of FDG-PET/CT scan and other biomarkers in predicting curative surgery. Complete resection of metastases will allow such patients to discontinue chemotherapy and live a normal life.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Adult patients, aged between 18 and 70 years with histologically proven adenocarcinoma or poorly differentiated carcinoma of the colon and rectum with unresectable liver-only metastases and no extra-hepatic disease.
  • World Health Organization (WHO) performance status of 0-
  • No previous chemotherapy for advanced disease.
  • Adequate functioning of the bone marrow, liver, and kidneys.

排除标准

  • Breastfeeding or pregnancy.
  • An active second primary cancer with the exception of squamous cell carcinoma of the skin or an in situ cancer.
  • Severe or uncompensated concomitant medical conditions.

研究组 & 干预措施

Single arm

Other

FOLFOXIRI and Bevacizumab

干预措施: FOLFOXIRI and Bevacizumab (Drug)

结局指标

主要结局

Rate of liver metastasectomy

时间窗: Up to 3 years from the date of enrolment into the study

Conversion From Unresectable To Resectable Liver Metastases

次要结局

  • 30 days rates of Grade III and IV toxicity(Up to 30 days of last cycle of FOLFOXIRI from the date of enrolment till the date of toxicity)
  • The European Organization for Research and Treatment of Cancer (EORTC) Colorectal Cancer Module (QLQ-CR29)(up to 3 years from the date of enrolment or till the progression of the disease)
  • The European Organization for Research and Treatment of Cancer (EORTC) Colorectal Liver Metastases Module (LMC21)(up to 3 years from the date of enrolment or till the progression of the disease)
  • Early-PET scan response(From the date of enrolment till 8 weeks after four cycles of FOLOXIRI and bevacizumab)
  • Progression-free survival(up to 5 years from the time of enrolment till disease progression or last follow up visit)
  • Response rate(Up to 12 weeks of last cycle of FOLFOXIRI from the date of enrolment till the date of maximum response)
  • The European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire Core 30 (QLQ-C30)(up to 3 years from the date of enrolment or till the progression of the disease)
  • Overall survival(up to 5 years from the time of enrolment till mortality or last follow up visit)

研究者

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

Shahid Ahmed

Professor of Medicine

University of Saskatchewan

研究点 (1)

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