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dc.contributor.authorSasaki, Kazunari
dc.contributor.authorWang, Jane
dc.contributor.authorKamphues, Carsten
dc.contributor.authorBuettner, Stefan
dc.contributor.authorGagniere, Johan
dc.contributor.authorArdilles, Victoria
dc.contributor.authorImai, Katsunori
dc.contributor.authorWagner, Doris
dc.contributor.authorPozios, Ioannis
dc.contributor.authorPapakonstantinou, Dimitris
dc.contributor.authorPikoulis, Emmanouil
dc.contributor.authorAntoniou, Efstathios
dc.contributor.authorMorioka, Daisuke
dc.contributor.authorLøes, Inger M.
dc.contributor.authorLønning, Per E.
dc.contributor.authorKornprat, Peter
dc.date.accessioned2025-04-30T20:18:35Z
dc.date.available2025-04-30T20:18:35Z
dc.date.issued2024-10-08
dc.identifier.urihttps://hdl.handle.net/1721.1/159220
dc.description.abstractBackground Recent studies have suggested that certain combinations of KRAS or BRAF biomarkers with clinical factors are associated with poor outcomes and may indicate that surgery could be “biologically” futile in otherwise technically resectable colorectal liver metastasis (CRLM). However, these combinations have yet to be validated through external studies. Patients and Methods We conducted a systematic search to identify these studies. The overall survival (OS) of patients with these combinations was evaluated in a cohort of patients treated at 11 tertiary centers. Additionally, the study investigated whether using high-risk KRAS point mutations in these combinations could be associated with particularly poor outcomes. Results The recommendations of four studies were validated in 1661 patients. The first three studies utilized KRAS, and their validation showed the following median and 5-year OS: (1) 30 months and 16.9%, (2) 24.3 months and 21.6%, and (3) 46.8 months and 44.4%, respectively. When analyzing only patients with high-risk KRAS mutations, median and 5-year OS decreased to: (1) 26.2 months and 0%, (2) 22.3 months and 15.1%, and (3) not reached and 44.9%, respectively. The fourth study utilized BRAF, and its validation showed a median OS of 10.4 months, with no survivors beyond 21 months. Conclusion The combinations of biomarkers and clinical factors proposed to render surgery for CRLM futile, as presented in studies 1 (KRAS high-risk mutations) and 4, appear justified. In these studies, there were no long-term survivors, and survival was similar to that of historic cohorts with similar mutational profiles that received systemic therapies alone for unresectable disease.en_US
dc.publisherSpringer International Publishingen_US
dc.relation.isversionofhttps://doi.org/10.1245/s10434-024-16319-0en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSpringer International Publishingen_US
dc.titleEvaluating Combinations of Biological and Clinicopathologic Factors Linked to Poor Outcomes in Resected Colorectal Liver Metastasis: An External Validation Studyen_US
dc.typeArticleen_US
dc.identifier.citationSasaki, K., Wang, J., Kamphues, C. et al. Evaluating Combinations of Biological and Clinicopathologic Factors Linked to Poor Outcomes in Resected Colorectal Liver Metastasis: An External Validation Study. Ann Surg Oncol 32, 408–417 (2025).en_US
dc.contributor.departmentSloan School of Managementen_US
dc.relation.journalAnnals of Surgical Oncologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2025-03-27T13:48:55Z
dc.language.rfc3066en
dc.rights.holderSociety of Surgical Oncology
dspace.embargo.termsY
dspace.date.submission2025-03-27T13:48:55Z
mit.journal.volume32en_US
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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