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dc.contributor.authorTonyali, Onder
dc.contributor.authorTastekin, Didem
dc.contributor.authorOzdemir, Nuriye
dc.contributor.authorUnal, Olcun Umit
dc.contributor.authorOflazoglu, Utku
dc.contributor.authorTurkmen, Esma
dc.contributor.authorErdogan, Bulent
dc.contributor.authorUyeturk, Ummugul
dc.contributor.authorOksuzoglu, Berna
dc.contributor.authorCinkir, Havva Yesil
dc.contributor.authorYasar, Nurgul
dc.contributor.authorGumus, Mahmut
dc.contributor.authorBerk, Veli
dc.contributor.authorKaplan, Mehmet Ali
dc.contributor.authorBuyukberber, Suleyman
dc.contributor.authorBalakan, Ozan
dc.contributor.authorÖZKAN, METİN
dc.contributor.authorDemirci, Umut
dc.contributor.authorOzturk, Turkan
dc.contributor.authorBilici, Ahmet
dc.date.accessioned2021-03-06T09:40:10Z
dc.date.available2021-03-06T09:40:10Z
dc.date.issued2013
dc.identifier.citationBerk V., Kaplan M. A. , Tonyali O., Buyukberber S., Balakan O., ÖZKAN M., Demirci U., Ozturk T., Bilici A., Tastekin D., et al., "Efficiency and Side Effects of Sorafenib Therapy for Advanced Hepatocellular Carcinoma: A Retrospective Study by the Anatolian Society of Medical Oncology", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, cilt.14, ss.7367-7369, 2013
dc.identifier.issn1513-7368
dc.identifier.otherav_e69d2273-7542-4d75-b806-8d3407983149
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/151693
dc.identifier.urihttps://doi.org/10.7314/apjcp.2013.14.12.7367
dc.description.abstractBackground: Inoperable and metastatic hepatocellular carcinoma (HCC) is associated with a poor prognosis and low chemotherapeutic efficiency. Sorafenib is an oral multi-kinase inhibitor exerting its effects via the RAF/MEK/ERK pathway, vascular endothelial growth factor receptor (VEGFR) and platelet derived growth factor receptor beta (PDGFR-beta) tyrosine kinases. Randomized studies have shown a significant contribution of sorafenib to life expectancy and quality of life of cancer patients. The aim of the present study is to evaluate the efficacy and side effects of sorafenib therapy in Turkey. Materials and Methods: Data for 103 patients (82 males, 21 females) receiving sorafenib therapy in 13 centers from February 2008 to December 2012 were evaluated. Median age was 61 years and median ECOG performance status was 1 (range: 0-2). 60 patients (58%) had hepatitis B, 15 patients (15%) had hepatitis C infection and 12 patients (12%) had a history of alcohol consumption. All of the patients had Child scores meeting the utilization permit of the drug in our country (Child A). Results: A total of 571 cycles of sorafenib therapy were administered with a median of four per patient. Among the evaluable cases, there was partial response in 15 (15%), stable disease in 52 (50%), and progressive disease in 36 (35%). Median progression-free survival was 18 weeks and median overall survival was 48 weeks. The dose was reduced only in 6 patients and discontinued in 2 patients due to grade 3-4 toxicity, 18 patients (17%) suffering hand-foot syndrome, 7 (7%) diarrhea, and 2 (2%) vomiting. Conclusions: This retrospective study demonstrated better efficacy of sorafenib therapy in patients with advanced HCC compared to the literature while progression-free survival and overall survival findings were comparable. The side effect rates indicate that the drug was tolerated well. In conclusion, among the available treatment options, sorafenib is an efficient and tolerable agent in patients with inoperable or metastatic HCC.
dc.language.isoeng
dc.subjectİç Hastalıkları
dc.subjectONKOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectOnkoloji
dc.titleEfficiency and Side Effects of Sorafenib Therapy for Advanced Hepatocellular Carcinoma: A Retrospective Study by the Anatolian Society of Medical Oncology
dc.typeMakale
dc.relation.journalASIAN PACIFIC JOURNAL OF CANCER PREVENTION
dc.contributor.departmentErciyes Üniversitesi , ,
dc.identifier.volume14
dc.identifier.issue12
dc.identifier.startpage7367
dc.identifier.endpage7369
dc.contributor.firstauthorID2358525


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