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.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* 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.
Exclusion Criteria:
* 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 be…
What they're measuring
1
Number of post-operative complications
Timeframe: 1 year
Trial details
NCT IDNCT02218801
SponsorEuropean Organisation for Research and Treatment of Cancer - EORTC