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Efficiency and Side Effects of Sorafenib Therapy for Advanced Hepatocellular Carcinoma: A Retrospective Study by the Anatolian Society of Medical Oncology

医学 索拉非尼 内科学 肝细胞癌 肿瘤科 进行性疾病 胃肠病学 回顾性队列研究 不利影响 外科 化疗
作者
Velı Berk,Kaplan Ma,Önder Tonyalı,Süleyman Büyükberber,Ozan Balakan,Metin Özkan,Umut Demırcı,Turkan Ozturk,Ahmet Bılıcı,Didem Taştekin,Nuriye Özdemir,Olçun Ümit Ünal,Utku Oflazoğlu,Esma Türkmen,Bülent Erdoğan,Ümmügül Üyetürk,Berna Öksüzoğlu,Havva Yeşil Çınkır,Nurgül Yaşar,Mahmut Gümüş
出处
期刊:Asian Pacific Journal of Cancer Prevention [West Asia Organization for Cancer Prevention]
卷期号:14 (12): 7367-7369 被引量:29
标识
DOI:10.7314/apjcp.2013.14.12.7367
摘要

Background: 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.

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