Characteristics and outcome of patients with dual hepatitis B and C-associated hepatocellular carcinoma: are they different from patients with single virus infection?

被引:16
|
作者
Huo, Teh-Ia [1 ,2 ]
Huang, Yi-Hsiang [3 ]
Hsia, Cheng-Yuan [4 ,5 ]
Su, Chien-Wei [5 ]
Lin, Han-Chieh [5 ]
Hsu, Chia-Yang [5 ]
Lee, Pui-Ching
Lui, Wing-Yiu [4 ,5 ]
Loong, Che-Chuan [4 ,5 ]
Chiang, Jen-Huei [5 ,6 ]
Chiou, Yi-You [5 ,6 ]
Lee, Shou-Dong [5 ]
机构
[1] Taipei Vet Gen Hosp, Dept Med, Div Gastroenterol, Taipei, Taiwan
[2] Natl Yang Ming Univ, Sch Med, Inst Pharmacol, Taipei 112, Taiwan
[3] Natl Yang Ming Univ, Sch Med, Inst Clin Med, Taipei 112, Taiwan
[4] Taipei Vet Gen Hosp, Dept Surg, Taipei, Taiwan
[5] Natl Yang Ming Univ, Sch Med, Fac Med, Taipei 112, Taiwan
[6] Taipei Vet Gen Hosp, Dept Radiol, Taipei, Taiwan
关键词
hepatitis B virus; hepatitis C virus; hepatocellular carcinoma; liver cirrhosis; STAGE LIVER-DISEASE; IMPACT; SUPERINFECTION; RECURRENCE; MANAGEMENT; ETIOLOGY; MODEL; RISK; TRANSPLANTATION; RESECTION;
D O I
10.1111/j.1478-3231.2008.01908.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Patients with hepatocellular carcinoma (HCC) caused by dual hepatitis B and C virus (HBV, HCV) infection may constitute a distinct disease group that is different from patients with single virus infection. This study compared the clinical characteristics and outcomes of patients with HBV, HCV and dual virus infection. A prospective database of 1215 HCC patients with chronic hepatitis B, C or dual virus infection was investigated. Patients with HCV infection (n=388) were significantly older (mean age, 69 years) than patients with dual virus (n=75, 65 years) and HBV (n=752; 60 years) infection (P < 0.0001). The male-to-female ratios for the HBV, dual virus and HCV groups were 5.2, 3.4 and 1.3 respectively (P < 0.0001). Patients in the HBV group more often had higher total tumour volume (mean, 409 cm(3)) than those in the dual virus group (244 cm(3)) and HCV (168 cm(3)) group (P < 0.0001). No significant differences of the severity of liver cirrhosis, performance status, cancer staging and tumour cell differentiation were noted among the three groups. Patients in the HCV group had a significantly poor survival in comparison with the HBV group only in the subset of patients with small tumour volume (< 50 cm(3)) in the Cox proportional hazards model (relative risk, 1.44; P=0.041). Dual HBV and HCV virus infection does not accelerate the speed of HCC formation in patients with chronic hepatitis B, and appears to have a modified course of carcinogenesis pathway that is diverted away from the biological behaviour of HBV and HCV infection.
引用
收藏
页码:767 / 773
页数:7
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