共 50 条
Long-term follow-up of patients with chronic hepatitis C with sustained virologic response to interferon
被引:10
|作者:
Ferreira, Sandro da Costa
[1
]
de Vasconcelos, Marcos
[1
]
Souza, Fernanda Fernandes
[1
]
Teixeira, Andreza Correa
[1
]
Villanova, Marcia Guimaraes
[1
]
de Castro, Jose Fernando
[2
]
Costa Passos, Afonso Dinis
[3
]
Zambelli Ramalho, Leandra Naira
[4
]
Zucoloto, Sergio
[4
]
Candolo Martinelli, Ana de Lourdes
[1
]
机构:
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Med, Div Gastroenterol, BR-14049900 Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Med, Div Infect Dis, BR-14049900 Ribeirao Preto, Brazil
[3] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Social Med, BR-14049900 Ribeirao Preto, Brazil
[4] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Pathol, Univ Hosp, BR-14049900 Ribeirao Preto, Brazil
来源:
关键词:
hepatitis C;
interferon;
HCV;
follow-up;
hepatocellular carcinoma;
HEPATOCELLULAR-CARCINOMA;
ALPHA THERAPY;
PLUS RIBAVIRIN;
HCV RNA;
HISTOLOGIC IMPROVEMENT;
INITIAL TREATMENT;
RANDOMIZED-TRIAL;
VIRUS-INFECTION;
COMBINATION;
PEGINTERFERON-ALPHA-2A;
D O I:
10.1590/S1413-86702010000400003
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Background and aim: The durability of the sustained virologic response (SVR) in patients with chronic hepatitis C after treatment and the ideal follow-up time for these patients remains undefined. The objective of the study was to evaluate the durability of the virologic response in patients with chronic hepatitis C followed up for at least 12 months after SVR at HCFMRP-USP. Methods: The study was conducted on 174 patients with chronic hepatitis C treated with different antiviral regimens who had achieved SVR. Qualitative serum HCV-RNA was determined by the commercial kit (COBAS AMPLICOR HCV, v2.0). Results: There was predominance of male (73%) with a mean age of 45.6 +/- 10 years. Liver cirrhosis was present in 16.1% of the study subjects. Mean follow-up time after SVR was 47 months (12-156 months). Twenty-two patients received monotherapy with interferon; 94 received interferon plus ribavirin, and 58 received pegylated interferon plus ribavirin. A total of 134 patients (77.0%) received one treatment course, 29 (16.7%) received two courses, and 11 (6.3%) received three courses. The distribution of HCV genotypes was: genotype 1 (40.2%), genotype 3 (40.8%) and genotype 2 (10.3%). Genotype was undetermined in 8.7% of cases. None of the 174 patients had recurrence of HCV infection. Two cirrhotic patients developed hepatocellular carcinoma (HCC) during follow-up. Conclusions: Among patients with SVR there was no recurrence of HCV infection or evidence of liver disease progression in any patient followed up for a mean of 47 months after SVR, except for patients with advanced hepatic disease before treatment, who may develop HCC despite SVR. Therefore, one can assume that SVR is associated with long term good prognosis.
引用
收藏
页码:330 / 334
页数:5
相关论文