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Background & Aims
Th
is study a
imed at develop
ing a pred
ict
ive algor
ith
m based on
interle
ukin 28B (
m>IL28Bm>) genotype, hepat
it
is C v
irus (HCV) genotype, and plas
ma HCV-RNA load, wh
ich could
accurately allow us to def
ine the probab
il
ity of response to pegylated
interferon (Peg-IFN) plus r
ibav
ir
in (RBV) therapy
in HIV/HCV-co
infected pat
ients.
Methods
Five hundred and twenty-one treatment-naive HIV-infected patients, who initiated HCV therapy with Peg-IFN/RBV, were analysed in an on-treatment basis. Patients were categorized as unlikely responders, uncertain responders, and anticipated responders (<20%, 20-60%, and >60%probability to achieve SVR, respectively).
Results
HCV genotype, baseline HCV-RNA load, and m>IL28Bm> genotype were confirmed as independent predictors of SVR in a logistic regression analysis. A stepwise algorithm based on these three variables was created based on 321 patients and evaluated in the remaining 200 patients. Unlikely responders included patients with genotype 1 or 4, HCV-RNA load 猢?00,000 IU/ml, and rs12979860 non-CC (rate of SVR: 17.3%). Anticipated responders were those with HCV genotype 2-3, patients harboring HCV genotype 4 and m>IL28Bm> CC, as well as those who simultaneously bore HCV genotype 1, HCV-RNA load <600,000 IU/ml, and m>IL28Bm> CC (rate of SVR 74.1%, 77.8%, and 64.4%, respectively). The area under the receiver operating characteristic curve of the model was 0.77 (0.733-0.814).
Conclusions
The combined use of m>IL28Bm> genotype, HCV genotype, and HCV-RNA load enables to easily identify patients with a high and very low likelihood of SVR. HCV therapy could be deferred in the latter patients, until more effective options are available, at least if they do not show advanced liver fibrosis.