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dc.contributor.authorKristensen, Annette T
dc.contributor.authorWiig, Johan N
dc.contributor.authorLarsen, Stein G
dc.contributor.authorGiercksky, Karl-Erik
dc.contributor.authorEkstrøm, Per O
dc.date.accessioned2015-10-09T02:10:05Z
dc.date.available2015-10-09T02:10:05Z
dc.date.issued2008
dc.identifier.citationBMC Cancer. 2008 Jul 27;8(1):213
dc.identifier.urihttp://hdl.handle.net/10852/46648
dc.description.abstractBackground After total mesorectal excision (TME) for rectal cancer around 10% of patients develops local recurrences within the pelvis. One reason for recurrence might be spillage of cancer cells during surgery. This pilot study was conducted to investigate the incidence of remnant cancer cells in pelvic lavage after resection of rectal cancer. DNA from cells obtained by lavage, were analysed by denaturing capillary electrophoresis with respect to mutations in hotspots of the k-ras gene, which are frequently mutated in colorectal cancer. Results Of the 237 rectal cancer patients analyzed, 19 had positive lavage fluid. There was a significant survival difference (p = 0.006) between patients with k-ras positive and negative lavage fluid. Conclusion Patients with k-ras mutated cells in the lavage immediately after surgery have a reduced life expectation. Detection of exfoliated cells in the abdominal cavity may be a useful diagnostic tool to improve the staging and eventually characterize patients who may benefit from aggressive multimodal treatment of rectal cancer.
dc.language.isoeng
dc.rightsKristensen et al.
dc.rightsAttribution 2.0 Generic
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/
dc.titleMolecular detection (k-ras) of exfoliated tumour cells in the pelvis is a prognostic factor after resection of rectal cancer?
dc.typeJournal article
dc.date.updated2015-10-09T02:10:06Z
dc.creator.authorKristensen, Annette T
dc.creator.authorWiig, Johan N
dc.creator.authorLarsen, Stein G
dc.creator.authorGiercksky, Karl-Erik
dc.creator.authorEkstrøm, Per O
dc.identifier.doihttp://dx.doi.org/10.1186/1471-2407-8-213
dc.identifier.urnURN:NBN:no-50823
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/46648/1/12885_2008_Article_1151.pdf
dc.type.versionPublishedVersion
cristin.articleid213


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