Multicenter Experience Using Telaprevir or Boceprevir With Peginterferon and Ribavirin to Treat Hepatitis C Genotype 1 After Liver Transplantation

被引:99
作者
Pungpapong, Surakit [1 ,2 ]
Aqel, Bashar A. [3 ]
Koning, Ludi [4 ,5 ]
Murphy, Jennifer L. [1 ]
Henry, Tanisha M. [1 ]
Ryland, Kristen L. [1 ]
Yataco, Maria L. [1 ,2 ]
Satyanarayana, Raj [1 ,2 ]
Rosser, Barry G. [1 ,2 ]
Vargas, Hugo E. [3 ]
Charlton, Michael R. [4 ]
Keaveny, Andrew P. [1 ,2 ]
机构
[1] Mayo Clin, Dept Transplantat, Jacksonville, FL 32224 USA
[2] Mayo Clin, Div Gastroenterol & Hepatol, Jacksonville, FL 32224 USA
[3] Mayo Clin, Div Gastroenterol & Hepatol, Scottsdale, AZ USA
[4] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[5] Erasmus MC Univ Med Ctr, Div Gastroenterol & Hepatol, Rotterdam, Netherlands
关键词
VIROLOGICAL RESPONSE; COMBINATION TREATMENT; TRIPLE THERAPY; VIRUS; CYCLOSPORINE; RECURRENCE; SAFETY; RECIPIENTS; INFECTION; EFFICACY;
D O I
10.1002/lt.23669
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The safety, efficacy, and effect on immunosuppression levels of telaprevir (TVR) or boceprevir (BOC) in combination with peginterferon (PEG-IFN) and ribavirin (RBV) in recipients of liver transplantation (LT) with hepatitis C virus (HCV) genotype 1 have not been defined. We report our 3 centers' preliminary experiences with administering triple antiviral treatment protocols containing PEG-IFN, RBV, and TVR or BOC. Patients with biopsy-proven HCV recurrence (METAVIR grade >= 3 and/or stage >= 2) received TVR with PEG-IFN/RBV for 12 weeks and then PEG-IFN/RBV for 36 weeks or BOC with PEG-IFN/RBV for 44 weeks after 4 weeks of lead-in PEG-IFN/RBV. Maintenance immunosuppression was changed to cyclosporine whenever possible, and the levels were followed closely. PEG-IFN/RBV dose adjustments were based on patients' tolerance. Sixty patients started triple antiviral treatment, and they were followed for up to 66 weeks (mean = 35 weeks); all were followed at least 12 weeks. Thirty of the 35 patients treated with TVR (86%) achieved undetectable HCV RNA levels after an average of 6 weeks, whereas 12 patients (48%) in the BOC-treated group achieved undetectable HCV RNA levels after a mean of 11 weeks. According to an intention-to-treat analysis, 14 of 21 TVR-treated patients (67%) and 10 of 22 patients who received BOC (45%) achieved undetectable HCV RNA levels at week 24 without viral breakthrough at the last follow-up. Cytopenias complicated both regimens; all patients required dose reductions of PEG-IFN and/or RBV or the administration of hematological growth factors. One death occurred in each group on triple antiviral treatment. In conclusion, TVR or BOC combined with PEG-IFN/RBV achieved on-treatment virological response rates of approximately 50% to 60% in patients with recurrent HCV after LT, but significant side effects were common. Liver Transpl 19:690-700, 2013. (C) 2013 AASLD.
引用
收藏
页码:690 / 700
页数:11
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