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肝细胞-胆管细胞癌:一种罕见原发性肝癌的人群水平分析

Combined hepatocellular-cholangiocarcinoma: a population-level analysis of an uncommon primary liver tumor.

作者信息

Garancini Mattia, Goffredo Paolo, Pagni Fabio, Romano Fabrizio, Roman Sanziana, Sosa Julie Ann, Giardini Vittorio

机构信息

Departments of General Surgery, San Gerardo Hospital, University of Milano-Bicocca, Monza, Italy.

出版信息

Liver Transpl. 2014 Aug;20(8):952-9. doi: 10.1002/lt.23897. Epub 2014 Jul 3.

Abstract

Combined hepatocellular-cholangiocarcinoma (cHCC-CC) is a rare primary liver cancer. Our aims were to analyze the demographic, clinical, and pathological characteristics of cHCC-CC at a population level and to investigate the effects of these features as well as different management strategies on the prognosis. The Surveillance, Epidemiology, and End Results (SEER) database was analyzed for 1988-2009. Data analyses were performed with chi-square tests, analyses of variance, Kaplan-Meier curves, and Cox proportional hazards regression. Four hundred sixty-five patients with cHCC-CC, 52,825 patients with hepatocellular carcinoma (HCC), and 7181 patients with cholangiocarcinoma (CC) were identified. cHCC-CC was more common in patients who were white, male, and older than 65 years. Treatment was more frequently nonsurgical/interventional. Patients with cHCC-CC, HCC, and CC had 5-year overall survival (OS) and disease-specific survival rates of 10.5%, 11.7%, and 5.7% (P < 0.001) and 17.8%, 21.0%, and 11.9% (P < 0.001), respectively. For cHCC-CC patients, an increasing invasiveness of the therapeutic approach was significantly associated with prolonged survival (P < 0.001). In a multivariate model, black race, a distant SEER stage, and a tumor size of 5.0 to 10.0 cm were independently associated with lower survival for cHCC-CC patients; a year of diagnosis after 1995 and surgical treatment with minor hepatectomy, major hepatectomy (MJH), or liver transplantation (LT) were independently associated with better survival for cHCC-CC patients. Patients diagnosed with cHCC-CC, HCC, and CC and treated with LT had 5-year OS rates of 41.1%, 67.0%, and 29.0%, respectively (P < 0.001). In conclusion, cHCC-CC patients appear to have intermediate demographic, clinical, and survival characteristics in comparison with HCC and CC patients. cHCC-CC patients undergoing LT showed inferior survival in comparison with HCC patients, and the role and indications for LT in cHCC-CC have yet to be defined. At this time, MJH may be considered the best therapeutic approach for such patients.

摘要

肝内胆管癌合并肝细胞癌(cHCC-CC)是一种罕见的原发性肝癌。我们的目的是在人群水平上分析cHCC-CC的人口统计学、临床和病理特征,并研究这些特征以及不同治疗策略对预后的影响。对监测、流行病学和最终结果(SEER)数据库1988 - 2009年的数据进行了分析。采用卡方检验、方差分析、Kaplan-Meier曲线和Cox比例风险回归进行数据分析。共识别出465例cHCC-CC患者、52825例肝细胞癌(HCC)患者和7181例胆管癌(CC)患者。cHCC-CC在白人、男性以及65岁以上患者中更为常见。治疗方式更常为非手术/介入性。cHCC-CC、HCC和CC患者的5年总生存率(OS)和疾病特异性生存率分别为10.5%、11.7%和5.7%(P < 0.001)以及17.8%、21.0%和11.9%(P < 0.001)。对于cHCC-CC患者,治疗方法侵袭性增加与生存期延长显著相关(P < 0.001)。在多变量模型中,黑人种族、远处SEER分期以及肿瘤大小为5.0至10.0 cm与cHCC-CC患者较低的生存率独立相关;1995年后诊断以及接受小范围肝切除术、大范围肝切除术(MJH)或肝移植(LT)的手术治疗与cHCC-CC患者较好的生存率独立相关。诊断为cHCC-CC、HCC和CC并接受LT治疗的患者5年OS率分别为41.1%、67.0%和29.0%(P < 0.001)。总之,与HCC和CC患者相比,cHCC-CC患者似乎具有中等的人口统计学、临床和生存特征。接受LT治疗的cHCC-CC患者与HCC患者相比生存率较低,LT在cHCC-CC中的作用和适应证尚未明确。目前,MJH可能被认为是此类患者的最佳治疗方法。

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