Page 84 - The Flying Publisher Guide to Hepatitis C Treatment
P. 84

84   | Hepatitis C Treatment

                                   achieved and 12 of 15 patients who were HCV RNA-negative
                                   before LT remained HCV RNA-negative ≥6 months
                                   postoperatively. The following predictors of response in these
                                   studies were identified: non-1 genotype, CTP class A (genotype 1
                                   only), ability to tolerate full dose and duration of treatment,
                                   lower pretreatment VL, a VL decrease ≥2 log 10  at week 4 of
                                   treatment (Alsatie 2007). Premature discontinuation of the
                                   therapy due to side effects was reported in 13-30% and dose
                                   reductions were more frequent.
                                    On the basis of available data, prophylactic antiviral therapy in
                                   this setting to prevent recurrent HCV infection post-LT has a
                                   limited role and may be associated with serious AEs.
                                   Pretransplant therapy, using a low-accelerating dose regimen, is
                                   an important treatment strategy but is applicable to selected
                                   patients only. Prophylactic antiviral therapy should not be
                                   considered in those with high MELD score (≥20) or CTP class B or
                                   C. It is to be noted that up to two-thirds of patients who become
                                   HCV RNA–negative on treatment will be HCV-free post-
                                   transplantation.

                                   Pre-emptive antiviral therapy after LT

                                    Preemptive antiviral therapy started within 2-6 weeks after
                                   transplantation has the advantage of a relatively low VL and the
                                   absence or minimal evidence of histologic recurrence, but is
                                   limited by tolerability, particularly in patients with high MELD
                                   scores pre-transplantation.
                                    Rates of SVR vary from 5% to 39% (Terrault 2008). Better results
                                   were reported in adult-to-adult right lobe live donor LT for HCC
                                   and low MELD scores as well as in planned living donor LT cases
                                   with splenectomy (Sugawara 2010). Dose reductions were
                                   required, more frequently for RBV than interferon, and
                                   treatment discontinuations were highly variable across the
                                   studies, ranging from 0% to 57%.
                                    Two small trials have evaluated the efficacy of PegIFN in this
                                   setting, one of which noted that only 41% of screened transplant
                                   recipients were eligible to begin therapy (Chalasani 2005).
   79   80   81   82   83   84   85   86   87   88   89