Longitudinal assessment of histology surrogate markers (FibroTest-ActiTest) during lamivudine therapy in patients with chronic hepatitis B infection

被引:105
作者
Poynard, T
Zoulim, F
Ratziu, V
Degos, F
Imbert-Bismut, F
Deny, P
Landais, P
El Hasnaoui, A
Slama, A
Blin, P
Thibault, V
Parvaz, P
Munteanu, M
Trepo, C
机构
[1] Grp Hosp Pitie Salpetriere, Dept Gastroenterol & Hepatol, F-75651 Paris, France
[2] Lyon Univ Hosp Ctr, Virol Lab, INSERM, U271,CNRS,UPRESA 8067, Lyon, France
[3] Hop Beaujon, Clichy, France
[4] Grp Hosp Pitie Salpetriere, Dept Biochem, F-75634 Paris, France
[5] Hop Avicenne, F-93009 Bobigny, France
[6] Hop Necker Enfants Malad, Paris, France
[7] GlaxoSmithKline Lab, Marly Le Roi, France
[8] Icare, Massy, France
[9] Grp Hosp Pitie Salpetriere, Dept Virol, F-75634 Paris, France
[10] Hospices Civils Lyon, Lab Hyg & Virol, Lyon, France
[11] Biopredictive, Paris, France
关键词
D O I
10.1111/j.1572-0241.2005.41957.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: The noninvasive serum markers, FibroTest-ActiTest (FT-AT), are an alternative to liver biopsy in patients with chronic hepatitis C and B. The aim was to use these markers in a prospective study of patients treated with lamivudine in order to assess the impact of treatment, as well as the factors associated with fibrosis progression. METHODS: Two hundred and ninety-eight patients were included in a prospective longitudinal study in 50 hospitals across France. FT-AT were measured at baseline, and then after 6, 12, and 24 months of lamivudine 100-mg treatment. Epidemiological, clinical, and virologic characteristics were analyzed by univariate and multivariate analysis. RESULTS: Two hundred and eighty-three patients were included for analysis. The accuracy of FT-AT versus biopsy was validated with the area under the ROC curve, 0.77 (SE = 0.03) for bridging fibrosis and 0.75 (SE = 0.06) for severe activity (A3). At baseline, bridging fibrosis (METAVIR stages F2-F3-F4) was highly associated (p < 0.001) in multivariate analysis with male gender and age and marginally associated with anti-HBe presence (p = 0.05) and non-Asian ethnic origin (p = 0.046). Lamivudine treatment had a very significant impact overall. FT decreased significantly from 0.51 at baseline to 0.37 at 24 months (p < 0.001), and 85% of patients had improvement at 24 months. AT also decreased significantly from 0.56 to 0.13 (p < 0.0001), and 91% of patients had improvement at 24 months. A three-phase kinetics was observed for both fibrosis and activity; there was a marked improvement during the first 6 months, followed by a plateau between 6 and 12 months, and another improvement between 12 and 24 months. The occurrence of a YMDD variant does not entirely explain these three-phase variations. The first phase impact on fibrosis rates was higher in Asian patients (p = 0.01) and in patients younger than 40 yr (p < 0.001). CONCLUSIONS: In patients with chronic hepatitis B, a 24-month course of lamivudine treatment leads to a significant decrease in necroinflammatory grades and fibrosis stages as assessed by noninvasive markers, with the occurrence of a three-phase kinetics. FT-AT should be useful in the noninvasive follow-up of lamivudine treatment.
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页码:1970 / 1980
页数:11
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