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索拉菲尼治疗晚期原发性肝癌的临床观察 被引量:5

Clinical observation of sorafenib monotherapy in patients with advanced primary liver cancer
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摘要 目的观察索拉菲尼治疗晚期原发性肝癌的临床疗效及毒性反应。方法21例晚期原发性肝癌患者口服索拉菲尼400mg,每日2次,6周为1个周期,直至病情进展或出现不可耐受的毒性反应。治疗6周后评定疗效和安全性。结果21例患者均完成6周治疗,其中部分缓解4例,病情稳定10例,病情进展7例,中位疾病进展时间为5.2个月。治疗期间发生手足皮肤反应者19例,其中1级10例,2级8例,3级1例;腹泻1级6例;恶心、呕吐1级5例;乏力1级3例;皮疹1级3例,2级7例;脱发1级4例;高血压1级1例;口炎1级1例。结论索拉菲尼治疗晚期原发性肝癌可控制肿瘤生长,不良反应可以耐受。 Objective To observe the efficacy and side effects of sorafenib monotherapy in patients with advanced primary liver cancer. Methods All 21 patients with advanced primary liver cancer were treated by sorafenib 400 mg twice daily, and the efficacy and side effects of sorafenib monotherapy were evaluated after sorafenib treatment for 6 weeks. Results Of 21 patients, 4 patients achieved partial remission, 10 patients achieved stable disease, and 7 patients achieved progression of disease ; time to progress was 5.2 months. The main side effects: 19 cases occurred hand-foot skin reaction, and grade one, two and three was in 10, 8 and 1 case, respectively; diarrhea was in 6 cases, and all were grade one; 5 cases undertook nausea/vomiting, and all was grade one ; skin rash was in 10 cases, and the grade one was 3 cases, grade two was 7 cases ; 4 cases was baldness ; lack of power, stomatitis and hypertension was in 1 case respectively, and all were grade one. Conclusion Sorafenib monotherapy in advanced primary liver cancer can control the growth of tumor.
出处 《中国医药》 2013年第2期191-192,共2页 China Medicine
关键词 肝肿瘤 晚期 原发性 索拉菲尼 毒性反应 Live tumor, advance, primary Sorafenib Toxic reaction
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  • 1Parkin DM,Bray F,Feday J. Global cancer statistics,2002[J].CA:A Cancer Journal for Clinicians,2005,(02):74-108.
  • 2Bruix J,Sherman M,Practice Guidelines Committee,American Association for the Study of Liver Diseases. Management of hepatocellular carcinoma[J].Hepatology,2005,(05):1208-1236.doi:10.1002/hep.20933.
  • 3Therasse P,Arbuck SG,Eisenhauer EA. New guidelines to evaluate the response to treatment in solid tumor European Organization for Research and Treatment of Cancer,National Cancer Institute of the United States,National Cancer Institute of Canada[J].Journal of the National Cancer Institute,2000,(03):205-216.doi:10.1093/jnci/92.3.205.
  • 4孙燕.内科肿瘤学[M]北京:人民卫生出版社,2001995-996.
  • 5Llovet JM,Ricci S,Mazzaferro V. Sorafenib in advanced hepatocellular carcinoma[J].New England Journal of Medicine,2008,(04):378-390.
  • 6Cheng AL,Kang YK,Chen Z. Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma:a phase Ⅲ randomised,double-blind,placebo-controlled trial[J].Lancet Oncology,2009,(01):25-34.doi:10.1016/S1470-2045(08)70285-7.
  • 7O'Dwyer PJ,Rosen M,Gallagher M. Pharmacodynamic study of BAY 43-9006 in patients with metastatic renal cell carcinoma[J].Proceedings of the American Society of Clinical Oncology,2005,(16S):193s.
  • 8Morin MJ. From oncogene to drug:development of small molecule tyrosine kinase inhibitors as anti-tumor and anti-angiogenic agents[J].Oncogene,2000,(56):6574-6583.
  • 9Strumberg D,Awada A,Hirte H. Pooled safety analysis of BAY 43-9006 (sorafenib) monotherapy in patients with advanced solid tumors:Is rash associated with treatment outcome[J].European Journal of Cancer,2006,(04):548-556.doi:10.1016/j.ejca.2005.11.014.

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