首页> 外文期刊>Journal of Hepatocellular Carcinoma >Hepatitis C virus-associated hepatocellular carcinoma as a second primary malignancy: exposing an overlooked presentation of liver cancer
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Hepatitis C virus-associated hepatocellular carcinoma as a second primary malignancy: exposing an overlooked presentation of liver cancer

机译:丙型肝炎病毒相关的肝细胞癌是第二大原发性恶性肿瘤:暴露了被忽视的肝癌表现

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Introduction: Chronic hepatitis C virus (HCV) infection is one of the leading causes of hepatocellular carcinoma (HCC) worldwide. Antiviral therapy in patients with HCV infection reduces the risk of primary HCC development by 71%–75%. HCV-infected patients with different primary cancers are also at risk for HCC development as a second primary malignancy (HCC-SPM). Limited information is available on the occurrence and characteristics of HCC-SPM. Herein, we determine the prevalence and clinical features of HCV-associated HCC-SPM when compared to primary HCC. Materials and methods: Patients with HCV-associated HCC seen at MD Anderson Cancer Center (2011–2017) were enrolled in a prospective observational study. Patients with multiple cancers diagnosed simultaneously or with hepatitis B virus or HIV coinfections were excluded. At enrollment, patients completed a questionnaire on medical history and HCC risk factors. Information on demographics, comorbidities, HCV treatment, tumor characteristics, treatment modalities, and virologic and oncologic outcomes were extracted from the medical records. Results: Among 171 consecutive patients with HCV-associated HCC enrolled, 26 (15%) had HCC-SPM. Most of the underlying primary cancers were solid tumors (85%). In 12 (46%) of these patients, the diagnosis was made incidentally while undergoing surveillance for primary malignancies, and the majority (81%) had their primary cancer in remission. Most patients (72%) with documented HCV viral load had chronic viremia due to lack of diagnosis, lack of treatment, or prior unsuccessful treatment of HCV infection and only 28% had undetectable viral load following successful antiviral therapy. The overall median survival for both groups was 29 months (95% CI: 23–35) without difference between groups ( p =0.2). Conclusion: Cancer patients with any malignancies must be screened for HCV as HCC-SPM can develop in 15% of infected patients. Early HCV diagnosis and treatment should be attempted to prevent the development of HCC-SPM, a condition associated with high mortality in cancer survivors.
机译:简介:慢性丙型肝炎病毒(HCV)感染是全球肝细胞癌(HCC)的主要原因之一。 HCV感染患者的抗病毒治疗可将原发性HCC发生的风险降低71%–75%。患有HCV感染的不同原发性癌症患者也有发生第二原发性恶性肿瘤(HCC-SPM)的危险。关于HCC-SPM的发生和特征的信息有限。在这里,我们确定与原发性肝癌相比,HCV相关性HCC-SPM的患病率和临床特征。材料和方法:在MD Anderson癌症中心(2011–2017)看到的HCV相关HCC患者被纳入一项前瞻性观察研究。同时诊断为多种癌症或乙型肝炎病毒或HIV合并感染的患者被排除在外。在入组时,患者填写了有关病史和HCC危险因素的问卷。有关人口统计学,合并症,HCV治疗,肿瘤特征,治疗方式以及病毒学和肿瘤学结果的信息均从病历中提取。结果:在连续纳入的171例HCV相关HCC患者中,有26例(15%)患有HCC-SPM。大多数潜在的原发癌是实体瘤(85%)。在这些患者中的12名(46%)中,在对原发性恶性肿瘤进行监测时偶然做出了诊断,并且大多数(81%)的原发性癌症已缓解。 HCV病毒载量已记录的大多数患者(72%)由于缺乏诊断,缺乏治疗或先前未成功治疗HCV感染而患有慢性病毒血症,成功抗病毒治疗后只有28%的患者检测不到病毒载量。两组的总中位生存期为29个月(95%CI:23–35),两组之间无差异(p = 0.2)。结论:必须筛查患有任何恶性肿瘤的癌症患者的HCV,因为15%的感染患者会发生HCC-SPM。应尝试早期HCV诊断和治疗,以预防HCC-SPM的发展,HCC-SPM是与癌症幸存者高死亡率相关的疾病。

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