Basit öğe kaydını göster

dc.contributor.authorOzaslan, Ersin
dc.contributor.authorTopaloglu, Ulas Serkan
dc.contributor.authorInanc, Mevlude
dc.contributor.authorErdem, Umut Gokmen
dc.contributor.authorDemir, Hacer
dc.contributor.authorArpaci, Erkan
dc.contributor.authorSeker, Mehmet Metin
dc.contributor.authorKaraaga, Mustafa
dc.contributor.authorKiziltepe, Melih
dc.contributor.authorEker, Baki
dc.contributor.authorOzkan, Metin
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:40:50Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:40:50Z
dc.date.issued2017
dc.identifier.issn1107-0625
dc.identifier.issn2241-6293
dc.identifier.urihttps://hdl.handle.net/20.500.12418/6730
dc.descriptionWOS: 000412789500007en_US
dc.descriptionPubMed ID: 29155512en_US
dc.description.abstractPurpose: To evaluate the efficacy and adverse events with cetuximab plus FOLFOX administered as second- and third-line therapy in metastatic colorectal cancer (mCRC) patients. Methods: IPatients were administered cetuximab plus FOLFOX as second- and third-line therapy from January 2010 through October 2015. mCRC patients with wild type KRAS were also given irinotecan and/or oxaliplatin combined with fluoropyrimidine +/- bevacizumab. Tumor response and survival were evaluated using RECIST and Kaplan-Meier method respectively. Results: Sixty patients were included this study. Cetuximab plus FOLFOX was administered to 40 (66.7%) patients as second-line and to 20 (33.3%) as third-line therapy. Themajority of the patients had a good ECOG performance status (PS) (0 or 1). Clinical benefit was partial plus stable disease and it was 75.0% for both of these two lines. The median progression free survival (PFS) was 7.1 months (95% CI=3.2-10.9) and 6.0 months (95% CI=2.4-9.6), in the second- and third-line (p=0.484). The median overall survival (OS) was 14.3 and 9.2 months in second- and third-line therapy respectively (p=0.071). The common toxicities were haematologic and gastrointestinal, mostly grade 1 and 2. Conclusion: The addition of cetuximab to FOLFOX was well-tolerated and had antitumor activity both in second and third-line therapy in patients with mCRC.en_US
dc.language.isoengen_US
dc.publisherIMPRIMATUR PUBLICATIONSen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectcetuximaben_US
dc.subjectchemotherapyen_US
dc.subjectcolorectal canceren_US
dc.subjectsecond lineen_US
dc.subjectthird lineen_US
dc.titleEfficacy and safety of cetuximab plus FOLFOX in second-line and third-line therapy in metastatic colorectal canceren_US
dc.typearticleen_US
dc.relation.journalJOURNAL OF BUONen_US
dc.contributor.department[Ozaslan, Ersin -- Inanc, Mevlude] Kayseri Training & Res Hosp, Dept Med Oncol, Kayseri, Turkey -- [Ozaslan, Ersin -- Inanc, Mevlude -- Ozkan, Metin] Erciyes Univ, Dept Med Oncol, Fac Med, Kayseri, Turkey -- [Topaloglu, Ulas Serkan -- Kiziltepe, Melih -- Eker, Baki] Kayseri Training & Res Hosp, Dept Internal Med, TR-38010 Kayseri, Turkey -- [Topaloglu, Ulas Serkan -- Kiziltepe, Melih] Erciyes Univ, Dept Internal Med, Fac Med, Kayseri, Turkey -- [Erdem, Umut Gokmen] Ankara Numune Training & Res Hosp, Dept Med Oncol, Ankara, Turkey -- [Demir, Hacer] Gazi Univ, Fac Med, Dept Med Oncol, Ankara, Turkey -- [Arpaci, Erkan] Bulent Ecevit Univ, Fac Med, Dept Med Oncol, Zonguldak, Turkey -- [Seker, Mehmet Metin] Cumhuriyet Univ, Fac Med, Dept Med Oncol, Sivas, Turkey -- [Karaaga, Mustafa] Necmettin Erbakan Univ, Meram Fac Med, Dept Med Oncol, Konya, Turkeyen_US
dc.identifier.volume22en_US
dc.identifier.issue4en_US
dc.identifier.endpage868en_US
dc.identifier.startpage863en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster