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dc.contributor.authorVarol, U.
dc.contributor.authorCirak, Y.
dc.contributor.authorCakar, B.
dc.contributor.authorKaraca, B.
dc.contributor.authorSezgin, C.
dc.contributor.authorUslu, R.
dc.contributor.authorKarabulut, B.
dc.date.accessioned2020-11-20T16:19:40Z
dc.date.available2020-11-20T16:19:40Z
dc.date.issued2013
dc.identifier.issn1107-0625
dc.identifier.issn2241-6293
dc.identifier.urihttps://hdl.handle.net/20.500.12809/3785
dc.descriptionCakar, Burcu/0000-0003-3790-791X; Karaca, Burcak/0000-0003-2638-1625; Uslu, Ruchan/0000-0002-9584-6134en_US
dc.descriptionWOS: 000325232400015en_US
dc.descriptionPubMed ID: 24065478en_US
dc.description.abstractPurpose: Exposure to all active agents may be more important than specific sequence of drug administration in the treatment of patients with metastatic colorectal cancer (mCRC). The purpose of this study was to evaluate the overall survival (OS) of mCRC patients who were treated with all 5 major therapeutic agents used in this malignancy. Methods: We retrospectively reviewed the medical records of 395 mCRC patients referred to our clinic. The study included patients who received 5-fluorouracil (5-FU)-, irinotecan- or oxaliplatin-based chemotherapy and at least 3 cycles of bevacizumab and 4 weeks of cetuximab sequentially in various combinations. Results: Forty mCRC patients received the 5 major therapeutic agents effectively and sequentially, and their mean OS was 26.43 +/- 2.04 months. The 3- and 4- year OS survival rates were 26.7% and 16.7%, respectively. When survival analysis was limited to the metastatic patients with at least 6 cycles of bevacizumab therapy in addition to standard duration of other chemotherapeutic agents (N=33), the mean OS was 26.7 +/- 2.38 months. With a further survival analysis limited to metastatic patients who were treated with at least both 6 cycles of bevacizumab and 8 weeks of cetuximab in addition to other therapies (N=17), the mean OS was 44.8 +/- 11.03 months. Conclusion: This study demonstrated that in mCRC patients there may be a significant survival advantage if an adequate tumor response was achieved with all major therapeutic agents. Therefore, we believe that we should treat our patients with the 5 major therapeutic drugs as effectively as possible.en_US
dc.item-language.isoengen_US
dc.publisherImprimatur Publicationsen_US
dc.item-rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBevacizumaben_US
dc.subjectCetuximaben_US
dc.subjectColorectal Canceren_US
dc.subject5-Fluorouracilen_US
dc.subjectIrinotecanen_US
dc.subjectOxaliplatinen_US
dc.titleSurvival analysis of metastatic colorectal cancer patients who were treated with the five major therapeutic agents over the course of diseaseen_US
dc.item-typearticleen_US
dc.contributor.departmenten_US
dc.contributor.departmentTemp[Varol, U.] Mugla Univ Res & Training Hosp, Dept Med Oncol, Mugla, Turkey -- [Cirak, Y.] Gaziantep Govt Hosp, Dept Med Oncol, Gaziantep, Turkey -- [Cakar, B.; Karaca, B.; Sezgin, C.; Uslu, R.; Karabulut, B.] Ege Univ, Fac Med, Dept Internal Med, Div Med Oncol, Bornova, Turkeyen_US
dc.identifier.volume18en_US
dc.identifier.issue3en_US
dc.identifier.startpage647en_US
dc.identifier.endpage652en_US
dc.relation.journalJournal of Buonen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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