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首页> 外文期刊>Infectious Agents and Cancer >Treatment of Recurrent Hepatocellular Carcinoma with Sorafenib in a HIV/HCV Co-Infected patient in HAART: A Case Report
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Treatment of Recurrent Hepatocellular Carcinoma with Sorafenib in a HIV/HCV Co-Infected patient in HAART: A Case Report

机译:索拉非尼在HIV / HCV合并感染的HAART患者中用索拉非尼治疗复发性肝癌:一例报告

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Background Liver disease is the second cause of death among HIV patients receiving highly active antiretroviral therapy (HAART) in Europe. HIV patients have a high prevalence of chronic HBV (6–10%) and HCV (33%) co-infection, and accelerated progression of viral hepatitis. Furthermore, the long duration of both HIV and HCV diseases in the HAART era increases the risk of hepatocellular carcinoma. Findings We report the case of a 49?year -old HIV/HCV co-infected male patient who developed hepatocellular carcinoma. The patient underwent a partial hepatectomy, and a few months later was treated with transcatheter arterial chemoembolisation due to hepatocarcinoma recurrence. Two months later, advanced hepatocellular carcinoma was diagnosed and sorafenib therapy was initiated. The patient achieved partial response of the main lesions, complete regression of the smallest lesions and did not experience clinical progression during the 20-month follow-up period. During therapy with sorafenib, the patient was treated with HAART with good viral and immunological responses. We used the therapeutic drug monitoring to assess antiretroviral concentrations during co-administration of sorafenib. Fosamprenavir Ctrough was found under the minimum level recommended by international guidelines. No grade 3 or 4 toxicities were observed. At month 20 of treatment, new liver lesions with portal vein thrombosis were diagnosed. After 28?months of sorafenib therapy, the patient deceased for severe liver insufficiency. Conclusions Sorafenib monotherapy demonstrated a marked delay in HCC disease progression in an HIV/HCV co-infected patient. Fosamprenavir Ctrough was found under the minimum level recommended by international guidelines, suggesting a possible interaction.
机译:背景技术在欧洲,在接受高活性抗逆转录病毒疗法(HAART)的HIV患者中,肝病是第二大死亡原因。 HIV患者的慢性HBV(6-10%)和HCV(33%)合并感染的患病率很高,并加速了病毒性肝炎的发展。此外,HAART时代HIV和HCV疾病的持续时间长,增加了肝细胞癌的风险。调查结果我们报告了一名49岁的HIV / HCV合并感染的男性患者,该患者发展为肝细胞癌。该患者接受了部分肝切除术,几个月后因肝癌复发而接受了经导管动脉化疗栓塞治疗。两个月后,诊断为晚期肝细胞癌并开始索拉非尼治疗。该患者在20个月的随访期内实现了主要病变的部分缓解,最小病变的完全消退,并且未经历临床进展。在用索拉非尼治疗期间,患者接受了具有良好病毒和免疫反应的HAART治疗。我们使用治疗药物监测来评估索拉非尼联合给药期间的抗逆转录病毒浓度。在国际准则建议的最低水平下发现了福沙那韦地槽。没有观察到3级或4级毒性。在治疗的第20个月,诊断出患有门静脉血栓的新肝损伤。索拉非尼治疗28个月后,患者因严重肝功能不全而死亡。结论索拉非尼单药治疗在HIV / HCV合并感染的患者中显示出HCC疾病进展的明显延迟。发现Fosamprenavir Ctrough的水平低于国际准则建议的最低水平,表明可能存在相互作用。

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