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dc.contributor.authorOcvirk, Janja
dc.contributor.authorBrodowicz, Thomas
dc.contributor.authorWrba, Fritz
dc.contributor.authorCiuleanu, Tudor E.
dc.contributor.authorKurteva, Galina
dc.contributor.authorBeslija, Semir
dc.contributor.authorKoza, Ivan
dc.contributor.authorZsuzsanna Papai
dc.contributor.authorMessinger, Diethelm
dc.contributor.authorYilmaz, Ugur
dc.contributor.authorZsolt Faluhelyi
dc.contributor.authorYalcin, Suayib
dc.contributor.authorPapamichael, Demetris
dc.contributor.authorMiklos Wenczl
dc.contributor.authorMrsic-Krmpotic, Zrinka
dc.contributor.authorShacham-Shmueli, Einat
dc.contributor.authorVrbanec, Damir
dc.contributor.authorEsser, Regina
dc.contributor.authorScheithauer, Werner
dc.contributor.authorZielinski, Christoph C.
dc.date.accessioned2019-12-10T11:10:44Z
dc.date.available2019-12-10T11:10:44Z
dc.date.issued2010
dc.identifier.issn1007-9327
dc.identifier.urihttps://doi.org/10.3748/wjg.v16.i25.3133
dc.identifier.urihttp://hdl.handle.net/11655/14902
dc.description.abstractAIM: To investigate efficacy and safety of cetuximab combined with two chemotherapy regimens in patients with unresectable metastatic colorectal cancer (mCRC). METHODS: Randomized patients received cetuximab with 5-fluorouracil (5-FU), folinic acid (FA) and oxaliplatin (FOLFOX) 6 (arm A, n = 74) or 5-FU, FA and irinotecan (FOLFIRI) (arm B, n = 77). KRAS mutation status was determined retrospectively in a subset of tumors (n = 117). RESULTS: No significant difference was found between treatment arms A and B in the progression-free survival (PFS) rate at 9 mo, 45% vs 34%; median PFS, 8.6 mo vs 8.3 mo [hazard ratio (HR) = 1.06]; overall response rate (ORR) 43% vs 45% [odds ratio (OR) = 0.93] and median overall survival (OS), 17.4 mo vs 18.9 mo (HR = 0.98). Patients with KRA5 wild-type tumors demonstrated improved PFS (HR = 0.55, P = 0.0051), OS, (HR = 0.62, P = 0.0296) and ORR (53% vs 36%) and in arm A, improved PFS (HR = 0.49, P = 0.0196), OS (HR = 0.48, P = 0.0201) and ORR (56% vs 30%), compared with patients with KRAS mutated tumors. In arm B no significant differences were found in efficacy by KRAS mutation status. Treatment in arms A and B was generally well tolerated. CONCLUSION: This study confirms that combinations of cetuximab with FOLFOX6 or FOLFIRI are effective and significantly improve clinical outcome in KRAS wild-type compared with KRAS mutated mCRC. (C) 2010 Baishideng. All rights reserved.
dc.language.isoen
dc.publisherBaishideng Publishing Group Inc
dc.relation.isversionof10.3748/wjg.v16.i25.3133
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGastroenterology & Hepatology
dc.titleCetuximab Plus Folfox6 Or Folfiri In Metastatic Colorectal Cancer: Cecog Trial
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalWorld Journal Of Gastroenterology
dc.contributor.departmentİç Hastalıkları
dc.identifier.volume16
dc.identifier.issue25
dc.identifier.startpage3133
dc.identifier.endpage3143
dc.description.indexWoS
dc.description.indexScopus


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