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Retreatment of hepatitis C patients with pegylated interferon combined with ribavirin in non-responders to interferon plus ribavirin. Is it different in real life?
被引:9
|作者:
Goncales, Fernando L., Jr.
[1
]
Moma, Camila A.
[1
]
Vigani, Aline G.
[1
]
Angerami, Adriana F. C. F.
[1
]
Goncales, Eduardo S. L.
[1
]
Tozzo, Raquel
[1
]
Pavan, Maria H. P.
[1
]
Goncales, Neiva S. L.
[1
,2
]
机构:
[1] Univ Estadual Campinas, UNICAMP, Grp Estudo Hepatites, Dept Clin Med,Fac Ciencias Med,Disciplina Doencas, Sao Paulo, Brazil
[2] Univ Estadual Campinas, UNICAMP, Ctr Hematol & Hemoterapia, Sao Paulo, Brazil
来源:
关键词:
PEGINTERFERON ALPHA-2A;
COMBINATION THERAPY;
D O I:
10.1186/1471-2334-10-212
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Background: More than 50% of hepatitis C viruses (HCV)-infected patients do not respond to the classical Interferon (IFN)/Ribavirin (RBV) combination therapy. The aim of this study was to evaluate the efficacy of retreatment with Peg-Interferon alpha-2b (PEG-IFN alpha-2b) plus RBV, in patients with HCV, genotypes 1 or 3, who were non-responders to the previous standard treatment with IFN/RBV. Methods: In the period 2005-2007, a total of 238 HCV chronic patients were non-responders to previous treatment with IFN plus RBV. Of these 130 agreed to be retreated with PEG-IFN alpha-2b and participated in this evaluation (90 with genotype 1 HCV and 40 with genotype 3 HCV). Patients were retreated at assisted IFN application hubs in compliance with the country's public health system rules. They received subcutaneous PEG-IFN alpha-2b, 1.5 mu g, once weekly, associated with RBV, through the oral route, with doses determined according to weight (1,000 mg if weight <= 75 kg and 1,250 mg if > 75 kg). Patients with genotype 1 HCV were retreated for over 48 weeks and patients with genotype 3 HCV for over 24 weeks. HCV-RNA was tested by polymerase chain reaction (PCR) at baseline, at week 12, at the end of the treatment, and 6 months thereafter. The predictiveness of week 12 in the development of a sustained virologic response (SVR) was also evaluated. Patients with negative HCV-RNA at week 12 were considered as early virologic responders (EVR). Results: EVR was observed in 25% of the patients with genotype 1 HCV and in 64% of the patients genotype 3 HCV (risk = 2.075 and p-value = 0.0414). SVR was observed in 22.2% of the patients with genotype 1 HCV and in 40% with genotype 3 HCV (intention-to-treat analysis). The positive predictive value (PPV) of the HCV-RNA testing at week 12, in order to obtain the SVR, was 65% for genotype 1 and 56% for genotype 3, and the negative predictive value (NPV) was 88% for genotype 1 and 89% for genotype 3. Conclusions: PEG-IFN alpha-2b plus weight-based ribavirin is effective in re-treating previous interferon-a plus RBV failure; 22.2% of the patients with genotype 1 HCV and 40% of patients with genotype 3 HCV achieved SVR.
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