Issue: 2007 > January > review

Evidence-base guideline on management of colorectal liver metastases in the Netherlands



REVIEW
S. Bipat, M.S. van Leeuwen, J.N.M. IJzermans, E.F.I. Comans, A.S.Th. Planting, P.M.M. Bossuyt, J-W. Greve, J. Stoker
AbstractPDF

Abstract

A dutch national evidence-based guideline on the
diagnosis and treatment of patients with colorectal liver
metastases has been developed. The most important
recommendations are as follows. For synchronous liver
metastases, spiral computed tomography (CT) or magnetic resonance imaging (MRI) should be used as imaging. For evaluation of lung metastases, imaging can be limited to chest radiography. For detection of metachronous liver metastases, ultrasonography could be performed as initial modality if the entire liver is adequately visualised. In doubtful cases or potential candidates for surgery, CT or MRI should be performed as additional imaging. For evaluation of extrahepatic disease, abdominal and chest CT could be performed. Fluorodeoxyglucose positron emission tomography could be valuable in patients selected for surgery based on CT (liver/abdomen/chest), for identifying additional extrahepatic disease. Surgical resection is the treatment of choice with a five-year survival of 30 to 40%. Variation in selection criteria for surgery is caused by inconclusive data in the literature concerning surgical margins <10 mm, presence of extrahepatic disease and the role of (neo)adjuvant therapy. To minimise variation in selection criteria, selection should be performed according to this guideline and preferably in qualified centres. If resection is not possible due to extensive disease, palliative chemotherapy is recommended. Systemic chemotherapy with fluoropyrimidine first-line chemotherapy (5-fu/leucovorin) combined with irinotecan or oxaliplatin should be considered as standard regimens. Radiofrequency ablation, isolated hepatic perfusion, portal vein embolisation, and
intra-arterial chemotherapy are considered experimental
and should only be performed as part of a clinical research protocol.