NCT02218801已完成不适用
A Prospective Colorectal Liver Metastasis Database With an Integrated Quality Assurance Program
European Organisation for Research and Treatment of Cancer - EORTC16 个研究点 分布在 12 个国家目标入组 219 人开始时间: 2015年5月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 219
- 试验地点
- 16
- 主要终点
- Number of post-operative complications
研究概览
简要总结
This prospective database has two main objectives;
- to evaluate the complication rates, 30-day and 90-day mortality from different surgical strategies for unresectable, borderline resectable or initially unresectable liver metastasis from colorectal cancer.
- to establish baseline quality parameters for different surgical strategies for unresectable, borderline and initially unresectable colorectal liver metastasis (CRLM) patients.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •With histologically proven colorectal adenocarcinoma with liver metastasis.
- •With unresectable, borderline or initially unresectable liver metastasis from a colorectal cancer assessed by a clinician or by a multi-disciplinary tumor board (MDT).
- •Unresectable is defined as no possibility of completely resecting all tumor due to size, location or number of deposits.
- •Borderline is defined as potentially operable but technically or biologically more challenging to resect as evaluated by the MDT.
- •Initially unresectable is defined as metastasis that have been down-sized after conversion chemotherapy and evaluated by the MDT to be resectable
- •discussed by a multidisciplinary team before surgery.
- •Participants of the MDT must include at least one liver surgeon, one radiologist and one oncologist. They will determine the resectability of the CRLM according to local practice.
- •With a possibility of a surgical procedure (resection with or without portal vein embolization, intraoperative local ablative technique or a combined approach) assessed during the MDT.
- •Age ≥ 18 years.
- •Before patient registration, written informed consent must be given according to ICH/GCP, and national/local regulations.
排除标准
- •Any psychological, familial, or sociological condition potentially hampering understanding of the research project.
- •Any other malignancy other than in situ carcinoma of the cervix or non-melanoma skin cancer (unless there has been a disease-free interval of at least 5 years)
结局指标
主要结局
Number of post-operative complications
时间窗: 1 year
次要结局
- Number of post-operative complications in the first 50 patients compared to the second 50 patients(1 year)
- Overall survival after 2 years of follow-up(3 years)
- Progression free survival at 2 years(3 years)
研究者
研究点 (16)
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