dc.contributor.author | Ocvirk, Janja | |
dc.contributor.author | Brodowicz, Thomas | |
dc.contributor.author | Wrba, Fritz | |
dc.contributor.author | Ciuleanu, Tudor E. | |
dc.contributor.author | Kurteva, Galina | |
dc.contributor.author | Beslija, Semir | |
dc.contributor.author | Koza, Ivan | |
dc.contributor.author | Zsuzsanna Papai | |
dc.contributor.author | Messinger, Diethelm | |
dc.contributor.author | Yilmaz, Ugur | |
dc.contributor.author | Zsolt Faluhelyi | |
dc.contributor.author | Yalcin, Suayib | |
dc.contributor.author | Papamichael, Demetris | |
dc.contributor.author | Miklos Wenczl | |
dc.contributor.author | Mrsic-Krmpotic, Zrinka | |
dc.contributor.author | Shacham-Shmueli, Einat | |
dc.contributor.author | Vrbanec, Damir | |
dc.contributor.author | Esser, Regina | |
dc.contributor.author | Scheithauer, Werner | |
dc.contributor.author | Zielinski, Christoph C. | |
dc.date.accessioned | 2019-12-10T11:10:44Z | |
dc.date.available | 2019-12-10T11:10:44Z | |
dc.date.issued | 2010 | |
dc.identifier.issn | 1007-9327 | |
dc.identifier.uri | https://doi.org/10.3748/wjg.v16.i25.3133 | |
dc.identifier.uri | http://hdl.handle.net/11655/14902 | |
dc.description.abstract | AIM: 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.iso | en | |
dc.publisher | Baishideng Publishing Group Inc | |
dc.relation.isversionof | 10.3748/wjg.v16.i25.3133 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Gastroenterology & Hepatology | |
dc.title | Cetuximab Plus Folfox6 Or Folfiri In Metastatic Colorectal Cancer: Cecog Trial | |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:eu-repo/semantics/publishedVersion | |
dc.relation.journal | World Journal Of Gastroenterology | |
dc.contributor.department | İç Hastalıkları | |
dc.identifier.volume | 16 | |
dc.identifier.issue | 25 | |
dc.identifier.startpage | 3133 | |
dc.identifier.endpage | 3143 | |
dc.description.index | WoS | |
dc.description.index | Scopus | |