Intensification with pegylated interferon during treatment with tenofovir in HIV-hepatitis B virus co-infected patients

被引:11
作者
Boyd, A. [1 ]
Piroth, L. [2 ,3 ]
Maylin, S. [4 ,5 ]
Maynard-Muet, M. [6 ]
Lebosse, F. [6 ]
Bouix, C.
Lascoux-Combe, C. [7 ]
Mahjoub, N. [4 ]
Girard, P. -M. [8 ,9 ]
Delaugerre, C. [4 ,5 ,10 ]
Carrat, F. [9 ,11 ]
Lacombe, K. [8 ,9 ]
Miailhes, P. [12 ,13 ]
机构
[1] INSERM, UMR_ S1136, Inst Pierre Louis Epidemiol & Sante Publ, Paris, France
[2] CHU, Dept Infectiol, Dijon, France
[3] Univ Bourgogne, UMR 1347, Dijon, France
[4] Hop St Louis, AP HP, Lab Virol, Paris, France
[5] Univ Paris Diderot, Paris, France
[6] Hospices Civils Lyon, Hop Croix Rousse, Serv Hepatol, INSERM U1052, Paris, France
[7] Hop St Louis, AP HP, Serv Malad Infectieuses & Trop, Paris, France
[8] Hop St Antoine, AP HP, Serv Malad Infectieuses & Trop, Paris, France
[9] UPMC Univ Paris 06, Inst Pierre Louis Epidemiol & Sante Publ, UMR_ S 1136, Sorbonne Univ, Paris, France
[10] INSERM, U941, Paris, France
[11] Hop St Antoine, AP HP, Dept Sante Publ, Lyon, France
[12] CNRS, Ctr Rech Canc Lyon, Equipes 15 & 16, INSERM,Unite 1052,UMR 5286, Lyon, France
[13] Hospices Civils Lyon, Serv Malad Infectieuses & Trop, Hop Croix Rousse, Lyon, France
关键词
chronic hepatitis B infection; HIV; pegylated interferon; time-dependent propensity score; treatment intensification; E-ANTIGEN; COINFECTED PATIENTS; SURFACE-ANTIGEN; HEPATOCELLULAR-CARCINOMA; TRANSIENT ELASTOGRAPHY; THERAPY; HBEAG; ENTECAVIR; HBV; QUANTIFICATION;
D O I
10.1111/jvh.12581
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In hepatitis B e antigen (HBeAg) positive patients with hepatitis B virus (HBV) mono-infection, intensification of nucleos(t)ide analogue treatment with pegylated interferon (PegIFN) could help induce higher HBeAg seroclearance rates. Our aim was to determine the long-term effect of adding PegIFN to tenofovir (TDF)-containing antiretroviral therapy on seroclearance in HBeAg-positive patients co-infected with the human immunodeficiency virus (HIV) and HBV. In this prospective matched cohort study, 46 patients with 1-year PegIFN intensification during TDF-containing antiretroviral therapy (TDF+PegIFN) were matched 1:1 to controls undergoing TDF without PegIFN (TDF) using a time-dependent propensity score based on age, CD4+ count and liver cirrhosis status. Kinetics of HBeAg quantification (qHBeAg) and hepatitis B surface antigen quantification (qHBsAg) were estimated using mixed-effect linear regression and time to HBeAg seroclearance or HBsAg seroclearance was modelled using proportional hazards regression. At baseline, previous TDF exposure was a median 39.8 months (IQR=21.4-59.4) and median qHBeAg and qHBsAg levels were 6.9PEIU/mL and 3.72 log(10)IU/mL, respectively (P>.5 between groups). Median follow-up was 33.4 months (IQR=19.0-36.3). During intensification, faster average declines of qHBeAg (-0.066 vs -0.027PEIU/mL/month, P=.001) and qHBsAg (-0.049 vs -0.026 log(10)IU/mL/month, P=.09) were observed in patients undergoing TDF+PegIFN vs TDF, respectively. After intensification, qHBeAg and qHBsAg decline was no different between groups (P=.7 and P=.9, respectively). Overall, no differences were observed in HBeAg seroclearance (TDF+PegIFN=13.2 vs TDF=12.6/100 personyears, P=.5) or HBsAg seroclearance rates (TDF+PegIFN=1.8 vs TDF=1.3/100 personyears, P=.7). In conclusion, PegIFN intensification in HBeAg-positive co-infected patients did not lead to increased rates of HBeAg or HBsAg clearance, despite faster declines of antigen levels while on PegIFN.
引用
收藏
页码:1017 / 1026
页数:10
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