PRELIMINARY RESULTS OF INDIVIDUAL THERAPY OF CHRONIC HEPATITIS C BY UKRAIN AND INTERFERON-α
VOLTCHEK I.,1 SOLOGUB T.,2 NOWICKY J.W.,3 GRIGORYEVA T.,2 BELOZYOROVA L.,2 BELOPOLSKAYA M.,2 SEMENYAKO N.,2 LAMANOVA E.2
1) Terra Medica Ltd., St. Petersburg, Russia.
2) Mechnikov Medical Academy, St. Petersburg, Russia.
3) Ukrainian Anti-Cancer Institute, Vienna, Austria.
Address for correspondence: I.V. Voltchek, Terra Medica Ltd., Zanevsky pr., 1, offices 253-255, 195196, Sf. Petersburg, Russia. Tel/fax: +7-812-4441051 E-mail: email@example.com
Summary: The effects of Ukrain and recombinant human interferon-α2b (IFN) on the state of the thiol-disulfide ratio (SH/SS) of the blood (Russian Federation patent no. 2150700) were studied in vitro using the amperometric titration method. The blood of 73 chronic hepatitis C (CHC) hepatitis C virus (HCV)-RNA-positive patients was examined. Ukrain was tested in doses of 0.05-2.0 μg/ml and IFN in 20-1000 U/ml of blood. After in vitro examination, 59 patients were treated: 28 with Ukrain and 31 with IFN. The first group of 16 patients (including eight with HCV genotype 1b) was treated with individually selected optimal doses of Ukrain (0.5-2.5 mg every second day). The second group of 12 patients was treated with doses of 2.5 mg Ukrain independent of in vitro test results. The third group of 31 patients was treated with individually selected optimal doses of IFN (0.5-2 MU 3 times a week). It was found that 79.4% of CHC patients were sensitive to Ukrain in vitro and 65.1% were sensitive to IFN. CHC patients with genotype 1b were sensitive to IFN only in 16.7% of cases while the figure for Ukrain was 92.3%. CHC patients with other HCV genotypes (3, 1a, 2) were sensitive to Ukrain in 86.7% of cases and to IFN in 70.6%. After 1 month of individual therapy with Ukrain, 87.5% of CHC patients, including six of eight cases with HCV genotype 1b, became PCR-HCV negative. In the group receiving the standard dose of Ukrain, virological response was only 33.3%. After 1 month, 74.2% of CHC patients treated with individual doses of IFN became PCR-HCV negative and after 3 months 90.3% were PCR-HCV negative. The prognostic significance of the method for screening preparations for the treatment of CHC patients was 89.8%. Treatment with Ukrain was without serious negative effects and the number of side effects of IFN in individual therapy was significantly reduced. Ukrain can be used in the treatment of CHC patients, alone or in combination with IFN preparations; in the cases with HCV genotype 1b Ukrain seems more promising than IFN. Individual therapy with Ukrain and IFN increased the efficacy of treatment 2.5-fold in comparison with standard monotherapy with the same preparations, significantly decreased the number of side effects and dramatically improved cost-effectiveness.