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Primary carcinoma of the liver: a study of 100 cases among 48,900 necropsies.原发性肝癌:48900例尸检中的100例研究。
Cancer. 1954 May;7(3):462-503. doi: 10.1002/1097-0142(195405)7:3<462::aid-cncr2820070308>3.0.co;2-e.
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Prognosis of hepatocellular carcinoma: the BCLC staging classification.肝细胞癌的预后:BCLC分期分类
Semin Liver Dis. 1999;19(3):329-38. doi: 10.1055/s-2007-1007122.
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A new prognostic classification for predicting survival in patients with hepatocellular carcinoma. Groupe d'Etude et de Traitement du Carcinome Hépatocellulaire.一种用于预测肝细胞癌患者生存率的新预后分类。肝细胞癌研究与治疗小组。
J Hepatol. 1999 Jul;31(1):133-41. doi: 10.1016/s0168-8278(99)80173-1.
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Rising incidence of hepatocellular carcinoma in the United States.美国肝细胞癌发病率不断上升。
N Engl J Med. 1999 Mar 11;340(10):745-50. doi: 10.1056/NEJM199903113401001.
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Characteristics of hepatocellular carcinoma in Italy.意大利肝细胞癌的特征。
J Hepatol. 1998 Dec;29(6):944-52. doi: 10.1016/s0168-8278(98)80122-0.
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Treatment of hepatocellular carcinoma associated with cirrhosis in the era of liver transplantation.肝移植时代肝细胞癌合并肝硬化的治疗
Ann Intern Med. 1998 Oct 15;129(8):643-53. doi: 10.7326/0003-4819-129-8-199810150-00013.
7
Natural history of untreated primary hepatocellular carcinoma: a retrospective study of 157 patients.未经治疗的原发性肝细胞癌的自然病史:一项对157例患者的回顾性研究。
Am J Clin Oncol. 1998 Aug;21(4):386-91. doi: 10.1097/00000421-199808000-00014.
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Treatment of hepatocellular carcinoma.肝细胞癌的治疗
Digestion. 1998 Aug;59(5):556-62. doi: 10.1159/000007531.
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[Hepatocellular carcinoma in Germany. Epidemiology, etiology, clinical aspects and prognosis in 100 consecutive patients of a university clinic].[德国的肝细胞癌。一所大学诊所100例连续患者的流行病学、病因、临床情况及预后]
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Hepatocellular carcinoma: from gene to public health.肝细胞癌:从基因到公共卫生
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中欧地区的肝细胞癌:预后特征与生存情况

Hepatocellular carcinoma in Central Europe: prognostic features and survival.

作者信息

Schöniger-Hekele M, Müller C, Kutilek M, Oesterreicher C, Ferenci P, Gangl A

机构信息

Universitätsklinik für Innere Medizin IV, Klinische Abteilung Gastroenterologie und Hepatologie, University of Vienna, Austria.

出版信息

Gut. 2001 Jan;48(1):103-9. doi: 10.1136/gut.48.1.103.

DOI:10.1136/gut.48.1.103
PMID:11115830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1728163/
Abstract

BACKGROUND AND AIMS

We investigated the influence of baseline characteristics of patients with hepatocellular carcinoma (HCC) on prognosis and developed a multivariate Cox model predicting survival. All patients were from Central Europe.

METHODS

All 245 patients seen at the Department of Gastroenterology and Hepatology at the University of Vienna, Austria, from July 1991 to March 1998 were included in this retrospective study. Nineteen different clinical characteristics and survival time from date of diagnosis were noted. Factors determining survival time were analysed by univariate and multivariate analysis using Cox proportional hazard regression models and a new classification model was constructed. The validity of this model was tested on an independent group of 89 patients, seen from April 1998 to September 1999.

RESULTS

Median survival in patients with HCC was 8.0 months. In a multivariate analysis bilirubin (>2 mg/dl), portal vein thrombosis, prothrombin time (<70%), alpha fetoprotein (>180 microg/l), tumour mass >50%, and enlarged lymph nodes were independent predictors of survival. A newly constructed Cox proportional hazard model (Vienna survival model for HCC=VISUM-HCC) identified three disease stages with different durations of survival (median survival stage 1, 15.2 months; stage 2, 7.2 months; and stage 3, 2.6 months; p=0.00001). Applying the VISUM-HCC survival model to patients in Okuda stage 2 identified subgroups with an excellent and very poor prognosis for which different treatment modalities should be offered.

CONCLUSIONS

Our patients with HCC had a poor median survival of eight months. Six easily measurable clinical variables were significant predictors of survival in patients with HCC. The new VISUM-HCC survival model may be useful for stratifying patients with HCC for various clinical treatment modalities.

摘要

背景与目的

我们研究了肝细胞癌(HCC)患者的基线特征对预后的影响,并建立了一个预测生存的多变量Cox模型。所有患者均来自中欧。

方法

本回顾性研究纳入了1991年7月至1998年3月在奥地利维也纳大学胃肠病学和肝病科就诊的所有245例患者。记录了19种不同的临床特征以及从诊断日期起的生存时间。使用Cox比例风险回归模型通过单变量和多变量分析来分析决定生存时间的因素,并构建了一个新的分类模型。该模型的有效性在1998年4月至1999年9月就诊的89例独立患者组中进行了测试。

结果

HCC患者的中位生存期为8.0个月。在多变量分析中,胆红素(>2mg/dl)、门静脉血栓形成、凝血酶原时间(<70%)、甲胎蛋白(>180μg/l)、肿瘤大小>50%以及淋巴结肿大是生存的独立预测因素。一个新构建的Cox比例风险模型(HCC维也纳生存模型=VISUM-HCC)确定了三个具有不同生存持续时间的疾病阶段(中位生存期:1期,15.2个月;2期,7.2个月;3期,2.6个月;p=0.00001)。将VISUM-HCC生存模型应用于奥田分期2期的患者,识别出了预后极好和极差的亚组,应针对这些亚组提供不同的治疗方式。

结论

我们的HCC患者中位生存期较差,为8个月。六个易于测量的临床变量是HCC患者生存的重要预测因素。新的VISUM-HCC生存模型可能有助于对HCC患者进行分层,以采用各种临床治疗方式。