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dc.contributor.authorOrdu, Cetin
dc.contributor.authorPilanci, Kezban Nur
dc.contributor.authorKoksal, Ulkuhan Iner
dc.contributor.authorOkutur, Kerem
dc.contributor.authorSaglam, Sezer
dc.contributor.authorTecimer, Coskun
dc.contributor.authorDemir, Gokhan
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T16:02:45Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T16:02:45Z
dc.date.issued2014
dc.identifier.issn1513-7368
dc.identifier.urihttps://dx.doi.org/10.7314/APJCP.2014.15.23.10165
dc.identifier.urihttp://hdl.handle.net/11446/2902
dc.descriptionWOS: 000351058400020en_US
dc.descriptionPubMed ID: 25556442en_US
dc.description.abstractBackground: Megestrol acetate (MA) is a steroid origin medicine often used for control of cachexia in oncologic palliative care. Thrombosis is a common problem in oncology patients. One question is whether MA can cause thrombosis. This retrospective, registry-based analysis was therefore conducted to assess thrombotic processes in oncology patients using MA concurrent with chemotherapy. Materials and Methods: Data on oncology patients at the metastatic stage using MA were obtained from the archives of our center. Outcomes of patients were evaluated for thromboembolic events (VTEs) during treatment. Results: Ninety-seven oncology patients with a median age of 62 (33-84) years were included. During the median follow-up of 17 months, 58 (59.8%) died leaving 39 (31.2%) still alive. Median overall survival (OS) was 19 months (6-180). Mean time of MA use was 8.69 months(+/- 3.53), with a median dose of 160mg (range 160-480mg). Eleven VTEs were detected after MA use, 4 of these in pancreatic cancer cases. The patients with thrombosis non-significantly had worse OS, than those without thrombosis (p=0.106). Conclusions: This trial revealed that the 11.3% of all patients developed thrombosis, who had been treated with MA and chemotherapy concomittantly. There was no statistically significant difference regarding to occurrence of thrombotic process, among the patients receiving different chemotherapy regimens with MA concomittantly. Pancreatic cancer seemed to be related to thrombosis rather than MA use.en_US
dc.language.isoengen_US
dc.publisherASIAN PACIFIC ORGANIZATION CANCER PREVENTIONen_US
dc.identifier.doi10.7314/APJCP.2014.15.23.10165en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMegestrol acetateen_US
dc.subjectoncologyen_US
dc.subjectthrombosisen_US
dc.subjectpalliative careen_US
dc.subjectcancer cachexiaen_US
dc.titleCan Megestrol Acetate Induce Thrombosis in Advanced Oncology Patients Receiving Chemotherapy?en_US
dc.typearticleen_US
dc.relation.journalASIAN PACIFIC JOURNAL OF CANCER PREVENTIONen_US
dc.departmentDBÜen_US
dc.identifier.issue23en_US
dc.identifier.volume15en_US
dc.identifier.startpage10165en_US
dc.identifier.endpage10169en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Ordu, Cetin -- Pilanci, Kezban Nur -- Koksal, Ulkuhan Iner -- Okutur, Kerem -- Saglam, Sezer -- Tecimer, Coskun -- Demir, Gokhan] Bilim Univ, Fac Med, Dept Med Oncol, Istanbul, Turkeyen_US


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