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dc.contributor.authorSalim Yüce
dc.contributor.authorMehmet Metin Şeker
dc.contributor.authorSema Koç
dc.contributor.authorİsmail Önder Uysal
dc.contributor.authorTurgut Kaçan
dc.contributor.authorMehtap Doğan
dc.contributor.authorMansur Doğan
dc.contributor.authorNalan Babacan Akgül
dc.contributor.authorSaadettin Kılıçkap
dc.date.accessioned23.07.201910:49:13
dc.date.accessioned2019-07-23T16:32:50Z
dc.date.available23.07.201910:49:13
dc.date.available2019-07-23T16:32:50Z
dc.date.issued2014
dc.identifier.issn1300-0144
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/TWpFek1USXpNdz09
dc.identifier.urihttps://hdl.handle.net/20.500.12418/2644
dc.description.abstractBackground/aim: Oxaliplatin is an effective and widely used chemotherapeutic agent in the treatment of many solid tumors. The most common side effects are peripheral neuropathy, gastrointestinal toxicity, and neutropenia. There have been some case reports about ototoxicity with oxaliplatin, but no clinical trials. In this trial, we explored whether or not oxaliplatin has ototoxic effects. Materials and methods: A total of 18 patients, 14 with colorectal cancer and 4 with pancreatic cancer, were included in this study. Four patients (22%) were treated with a capecitabine and oxaliplatin (CapeOx) regimen, and 14 patients (78%) were treated with fluorouracil, leucovorin, and oxaliplatin (FOLFOX-6). Patients’ pretreatment and posttreatment hearing levels were assessed with high-frequency audiometry and otoacoustic emission tests. Results: The median time between the first and the last oxaliplatin doses was 3.2 months (range: 2–7 months). There was no hearing loss in tests conducted for both ears of patients at frequencies of 500, 1000, 2000, 4000, 6000, 8000, 12,000, and 16,000 Hz. There was no difference between the pretreatment and posttreatment otoacoustic emission tests. Conclusion: Oxaliplatin is a reliable agent in terms of ototoxicityen_US
dc.description.abstractBackground/aim: Oxaliplatin is an effective and widely used chemotherapeutic agent in the treatment of many solid tumors. The most common side effects are peripheral neuropathy, gastrointestinal toxicity, and neutropenia. There have been some case reports about ototoxicity with oxaliplatin, but no clinical trials. In this trial, we explored whether or not oxaliplatin has ototoxic effects. Materials and methods: A total of 18 patients, 14 with colorectal cancer and 4 with pancreatic cancer, were included in this study. Four patients (22%) were treated with a capecitabine and oxaliplatin (CapeOx) regimen, and 14 patients (78%) were treated with fluorouracil, leucovorin, and oxaliplatin (FOLFOX-6). Patients’ pretreatment and posttreatment hearing levels were assessed with high-frequency audiometry and otoacoustic emission tests. Results: The median time between the first and the last oxaliplatin doses was 3.2 months (range: 2–7 months). There was no hearing loss in tests conducted for both ears of patients at frequencies of 500, 1000, 2000, 4000, 6000, 8000, 12,000, and 16,000 Hz. There was no difference between the pretreatment and posttreatment otoacoustic emission tests. Conclusion: Oxaliplatin is a reliable agent in terms of ototoxicityen_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCerrahien_US
dc.titleOxaliplatin and ototoxicity: is it really safe for hearing?en_US
dc.typearticleen_US
dc.relation.journalTurkish Journal of Medical Sciencesen_US
dc.contributor.departmentSivas Cumhuriyet Üniversitesien_US
dc.identifier.volume44en_US
dc.identifier.issue4en_US
dc.identifier.endpage589en_US
dc.identifier.startpage586en_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US]


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