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2. The present and future disease burden of hepatitis C virus (HCV) infections with todayʼs treatment paradigm – volume 2

Author

Hatzakis, A., Chulanov, V., Gadano, A. C., Bergin, C., Ben-Ari, Z., Mossong, J., Schréter, I., Baatarkhuu, O., Acharya, S., Aho, I., Anand, A. C., Andersson, M. I., Arendt, V., Arkkila, P., Barclay, K., Bessone, F., Blach, S., Blokhina, N., Brunton, C. R., Choudhuri, G., Cisneros, L., Croes, E. A., Dahgwahdorj, Y. A., Dalgard, O., Daruich, J. R., Dashdorj, N. R., Davaadorj, D., de Knegt, R. J., de Vree, M., Estes, C., Flisiak, R., Gane, E., Gower, E., Halota, W., Henderson, C., Hoffmann, P., Hornell, J., Houlihan, D., Hrusovsky, S., Jarčuška, P., Kershenobich, D., Kostrzewska, K., Kristian, P., Leshno, M., Lurie, Y., Mahomed, A., Mamonova, N., Mendez-Sanchez, N., Norris, S., Nurmukhametova, E., Nymadawa, P., Oltman, M., Oyunbileg, J., Oyunsuren, Ts., Papatheodoridis, G., Pimenov, N., Prabdial-Sing, N., Prins, M., Radke, S., Rakhmanova, A., Razavi-Shearer, K., Reesink, H. W., Ridruejo, E., Safadi, R., Sagalova, O., Avila, Sanchez J. F., Sanduijav, R., Saraswat, V., Seguin-Devaux, C., Shah, S. R., Shestakova, I., Shevaldin, A., Shibolet, O., Silva, M. O., Sokolov, S., Sonderup, M., Souliotis, K., Spearman, C. W., Staub, T., Stedman, C., Strebkova, E. A., Struck, D., Sypsa, V., Tomasiewicz, K., Undram, L., van der Meer, A. J., van Santen, D., Veldhuijzen, I., Villamil, F. G., Willemse, S., Zuckerman, E., Zuure, F. R., Puri, P., and Razavi, H.

Published
2015
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3. Strategies to manage hepatitis C virus (HCV) infection disease burden – volume 2

Author

Gane, E., Kershenobich, D., Seguin-Devaux, C., Kristian, P., Aho, I., Dalgard, O., Shestakova, I., Nymadawa, P., Blach, S., Acharya, S., Anand, A. C., Andersson, M. I., Arendt, V., Arkkila, P., Baatarkhuu, O., Barclay, K., Ben-Ari, Z., Bergin, C., Bessone, F., Blokhina, N., Brunton, C. R., Choudhuri, G., Chulanov, V., Cisneros, L., Croes, E. A., Dahgwahdorj, Y. A., Daruich, J. R., Dashdorj, N. R., Davaadorj, D., de Knegt, R. J., de Vree, M., Gadano, A. C., Gower, E., Halota, W., Hatzakis, A., Henderson, C., Hoffmann, P., Hornell, J., Houlihan, D., Hrusovsky, S., Jarčuška, P., Kostrzewska, K., Leshno, M., Lurie, Y., Mahomed, A., Mamonova, N., Mendez-Sanchez, N., Mossong, J., Norris, S., Nurmukhametova, E., Oltman, M., Oyunbileg, J., Oyunsuren, Ts., Papatheodoridis, G., Pimenov, N., Prins, M., Puri, P., Radke, S., Rakhmanova, A., Razavi, H., Razavi-Shearer, K., Reesink, H. W., Ridruejo, E., Safadi, R., Sagalova, O., Avila, Sanchez J. F., Sanduijav, R., Saraswat, V., Schréter, I., Shah, S. R., Shevaldin, A., Shibolet, O., Silva, M. O., Sokolov, S., Sonderup, M., Souliotis, K., Spearman, C. W., Staub, T., Stedman, C., Strebkova, E. A., Struck, D., Sypsa, V., Tomasiewicz, K., Undram, L., van der Meer, A. J., van Santen, D., Veldhuijzen, I., Villamil, F. G., Willemse, S., Zuckerman, E., Zuure, F. R., Prabdial-Sing, N., Flisiak, R., and Estes, C.

Published
2015
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4. Historical epidemiology of hepatitis C virus (HCV) in select countries – volume 2

Author

Saraswat, V., Norris, S., de Knegt, R. J., Avila, Sanchez J. F., Sonderup, M., Zuckerman, E., Arkkila, P., Stedman, C., Acharya, S., Aho, I., Anand, A. C., Andersson, M. I., Arendt, V., Baatarkhuu, O., Barclay, K., Ben-Ari, Z., Bergin, C., Bessone, F., Blach, S., Blokhina, N., Brunton, C. R., Choudhuri, G., Chulanov, V., Cisneros, L., Croes, E. A., Dahgwahdorj, Y. A., Dalgard, O., Daruich, J. R., Dashdorj, N. R., Davaadorj, D., de Vree, M., Estes, C., Flisiak, R., Gadano, A. C., Gane, E., Halota, W., Hatzakis, A., Henderson, C., Hoffmann, P., Hornell, J., Houlihan, D., Hrusovsky, S., Jarčuška, P., Kershenobich, D., Kostrzewska, K., Kristian, P., Leshno, M., Lurie, Y., Mahomed, A., Mamonova, N., Mendez-Sanchez, N., Mossong, J., Nurmukhametova, E., Nymadawa, P., Oltman, M., Oyunbileg, J., Oyunsuren, Ts., Papatheodoridis, G., Pimenov, N., Prabdial-Sing, N., Prins, M., Puri, P., Radke, S., Rakhmanova, A., Razavi, H., Razavi-Shearer, K., Reesink, H. W., Ridruejo, E., Safadi, R., Sagalova, O., Sanduijav, R., Schréter, I., Seguin-Devaux, C., Shah, S. R., Shestakova, I., Shevaldin, A., Shibolet, O., Sokolov, S., Souliotis, K., Spearman, C. W., Staub, T., Strebkova, E. A., Struck, D., Tomasiewicz, K., Undram, L., van der Meer, A. J., van Santen, D., Veldhuijzen, I., Villamil, F. G., Willemse, S., Zuure, F. R., Silva, M. O., Sypsa, V., and Gower, E.

Published
2015
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7. Use of noninvasive biomarkers to assess fibrosis regression in cirrhotic patients during nucleos(t)ide therapy

Author

Pan, C., primary, Izumi, N., additional, Angus, P., additional, Duseja, A., additional, Nurmukhametova, E., additional, Balabanska, R., additional, Nguyen, T., additional, Yang, J., additional, Lin, L., additional, Gaggar, A., additional, Flaherty, J.F., additional, Subramanian, M., additional, Ryder, S., additional, Chuang, W.-L., additional, and Marcellin, P., additional

Published
2018
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8. The present and future disease burden of hepatitis C virus (HCV) infections with today's treatment paradigm - volume 2

Author

Hatzakis, A. Chulanov, V. Gadano, A. C. Bergin, C. and Ben-Ari, Z. Mossong, J. Schreter, I. Baatarkhuu, O. and Acharya, S. Aho, I. Anand, A. C. Andersson, M. I. and Arendt, V. Arkkila, P. Barclay, K. Bessone, F. Blach, S. and Blokhina, N. Brunton, C. R. Choudhuri, G. Cisneros, L. and Croes, E. A. Dahgwahdorj, Y. A. Dalgard, O. Daruich, J. R. Dashdorj, N. R. Davaadorj, D. de Knegt, R. J. de Vree, M. Estes, C. Flisiak, R. Gane, E. Gower, E. and Halota, W. Henderson, C. Hoffmann, P. Hornell, J. and Houlihan, D. Hrusovsky, S. Jarcuska, P. Kershenobich, D. and Kostrzewska, K. Kristian, P. Leshno, M. Lurie, Y. and Mahomed, A. Mamonova, N. Mendez-Sanchez, N. Norris, S. and Nurmukhametova, E. Nymadawa, P. Oltman, M. Oyunbileg, J. and Oyunsuren, Ts. Papatheodoridis, G. Pimenov, N. and Prabdial-Sing, N. Prins, M. Radke, S. Rakhmanova, A. and Razavi-Shearer, K. Reesink, H. W. Ridruejo, E. Safadi, R. and Sagalova, O. Sanchez Avila, J. F. Sanduijav, R. and Saraswat, V. Seguin-Devaux, C. Shah, S. R. Shestakova, I. and Shevaldin, A. Shibolet, O. Silva, M. O. Sokolov, S. and Sonderup, M. Souliotis, K. Spearman, C. W. Staub, T. and Stedman, C. Strebkova, E. A. Struck, D. Sypsa, V. and Tomasiewicz, K. Undram, L. van der Meer, A. J. van Santen, D. Veldhuijzen, I. Villamil, F. G. Willemse, S. and Zuckerman, E. Zuure, F. R. Puri, P. Razavi, H.

Abstract

Morbidity and mortality attributable to chronic hepatitis C virus (HCV) infection are increasing in many countries as the infected population ages. Models were developed for 15 countries to quantify and characterize the viremic population, as well as estimate the number of new infections and HCV related deaths from 2013 to 2030. Expert consensus was used to determine current treatment levels and outcomes in each country. In most countries, viremic prevalence has already peaked. In every country studied, prevalence begins to decline before 2030, when current treatment levels were held constant. In contrast, cases of advanced liver disease and liver related deaths will continue to increase through 2030 in most countries. The current treatment paradigm is inadequate if large reductions in HCV related morbidity and mortality are to be achieved.

Published
2015

9. Historical epidemiology of hepatitis C virus (HCV) in select countries - volume 2

Author

Saraswat, V. Norris, S. de Knegt, R. J. Sanchez Avila, J. F. and Sonderup, M. Zuckerman, E. Arkkila, P. Stedman, C. and Acharya, S. Aho, I. Anand, A. C. Andersson, M. I. and Arendt, V. Baatarkhuu, O. Barclay, K. Ben-Ari, Z. and Bergin, C. Bessone, F. Blach, S. Blokhina, N. Brunton, C. R. Choudhuri, G. Chulanov, V. Cisneros, L. Croes, E. A. Dahgwahdorj, Y. A. Dalgard, O. Daruich, J. R. and Dashdorj, N. R. Davaadorj, D. de Vree, M. Estes, C. and Flisiak, R. Gadano, A. C. Gane, E. Halota, W. Hatzakis, A. Henderson, C. Hoffmann, P. Hornell, J. Houlihan, D. and Hrusovsky, S. Jarcuska, P. Kershenobich, D. Kostrzewska, K. Kristian, P. Leshno, M. Lurie, Y. Mahomed, A. and Mamonova, N. Mendez-Sanchez, N. Mossong, J. Nurmukhametova, E. Nymadawa, P. Oltman, M. Oyunbileg, J. Oyunsuren, Ts. and Papatheodoridis, G. Pimenov, N. Prabdial-Sing, N. Prins, M. Puri, P. Radke, S. Rakhmanova, A. Razavi, H. and Razavi-Shearer, K. Reesink, H. W. Ridruejo, E. Safadi, R. and Sagalova, O. Sanduijav, R. Schreter, I. Seguin-Devaux, C. Shah, S. R. Shestakova, I. Shevaldin, A. Shibolet, O. and Sokolov, S. Souliotis, K. Spearman, C. W. Staub, T. and Strebkova, E. A. Struck, D. Tomasiewicz, K. Undram, L. and van der Meer, A. J. van Santen, D. Veldhuijzen, I. Villamil, F. G. Willemse, S. Zuure, F. R. Silva, M. O. Sypsa, V. and Gower, E.

Abstract

Chronic hepatitis C virus (HCV) infection is a leading cause of liver related morbidity and mortality. In many countries, there is a lack of comprehensive epidemiological data that are crucial in implementing disease control measures as new treatment options become available. Published literature, unpublished data and expert consensus were used to determine key parameters, including prevalence, viremia, genotype and the number of patients diagnosed and treated. In this study of 15 countries, viremic prevalence ranged from 0.13% in the Netherlands to 2.91% in Russia. The largest viremic populations were in India (8666000 cases) and Russia (4162000 cases). In most countries, males had a higher rate of infections, likely due to higher rates of injection drug use (IDU). Estimates characterizing the infected population are critical to focus screening and treatment efforts as new therapeutic options become available.

Published
2015

10. Strategies to manage hepatitis C virus (HCV) infection disease burden - volume 2

Author

Gane, E. Kershenobich, D. Seguin-Devaux, C. Kristian, P. and Aho, I. Dalgard, O. Shestakova, I. Nymadawa, P. Blach, S. Acharya, S. Anand, A. C. Andersson, M. I. Arendt, V. and Arkkila, P. Baatarkhuu, O. Barclay, K. Ben-Ari, Z. and Bergin, C. Bessone, F. Blokhina, N. Brunton, C. R. and Choudhuri, G. Chulanov, V. Cisneros, L. Croes, E. A. and Dahgwahdorj, Y. A. Daruich, J. R. Dashdorj, N. R. Davaadorj, D. de Knegt, R. J. de Vree, M. Gadano, A. C. Gower, E. and Halota, W. Hatzakis, A. Henderson, C. Hoffmann, P. and Hornell, J. Houlihan, D. Hrusovsky, S. Jarcuska, P. and Kostrzewska, K. Leshno, M. Lurie, Y. Mahomed, A. and Mamonova, N. Mendez-Sanchez, N. Mossong, J. Norris, S. and Nurmukhametova, E. Oltman, M. Oyunbileg, J. Oyunsuren, Ts. and Papatheodoridis, G. Pimenov, N. Prins, M. Puri, P. and Radke, S. Rakhmanova, A. Razavi, H. Razavi-Shearer, K. and Reesink, H. W. Ridruejo, E. Safadi, R. Sagalova, O. and Sanchez Avila, J. F. Sanduijav, R. Saraswat, V. Schreter, I. and Shah, S. R. Shevaldin, A. Shibolet, O. Silva, M. O. and Sokolov, S. Sonderup, M. Souliotis, K. Spearman, C. W. and Staub, T. Stedman, C. Strebkova, E. A. Struck, D. Sypsa, V. Tomasiewicz, K. Undram, L. van der Meer, A. J. van Santen, D. Veldhuijzen, I. Villamil, F. G. Willemse, S. and Zuckerman, E. Zuure, F. R. Prabdial-Sing, N. Flisiak, R. and Estes, C.

Abstract

The hepatitis C virus (HCV) epidemic was forecasted through 2030 for 15 countries, and the relative impact of two scenarios was considered: (i) increased treatment efficacy while holding the treated population constant and (ii) increased treatment efficacy and increased annual treated population. Increasing levels of diagnosis and treatment, in combination with improved treatment efficacy, were critical for achieving substantial reductions in disease burden. In most countries, the annual treated population had to increase several fold to achieve the largest reductions in HCV-related morbidity and mortality. This suggests that increased capacity for screening and treatment will be critical in many countries. Birth cohort screening is a helpful tool for maximizing resources. In most of the studied countries, the majority of patients were born between 1945 and 1985.

Published
2015

12. P1285 : Forecasting the disease burden of chronic hepatitis C in Russia

Author

Chulanov, V., primary, Sagalova, O., additional, Blokhina, N., additional, Mamonova, N., additional, Nurmukhametova, E., additional, Pimenov, N., additional, Rakhmanova, A., additional, Razavi, H., additional, Razavi-Shearer, K., additional, Shevaldin, A., additional, Chesnokov, E., additional, Sokolov, S., additional, Strebkova, E., additional, Znoiko, O., additional, and Shestakova, I., additional

Published
2015
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15. Sofosbuvir/velpatasvir for the treatment of HCV: excellent results from a phase-3, open-label study in Russia and Sweden.

Author

Isakov V, Chulanov V, Abdurakhmanov D, Burnevich E, Nurmukhametova E, Kozhevnikova G, Gankina N, Zhuravel S, Romanova S, Hyland RH, Lu S, Svarovskaia ES, McNally J, Brainard DM, Ivashkin V, Morozov V, Bakulin I, Lagging M, Zhdanov K, and Weiland O

Subjects
Adolescent, Adult, Aged, Antiviral Agents administration & dosage, Carbamates administration & dosage, Drug Therapy, Combination, Female, Heterocyclic Compounds, 4 or More Rings administration & dosage, Humans, Male, Middle Aged, Russia, Sofosbuvir administration & dosage, Sweden, Young Adult, Antiviral Agents therapeutic use, Carbamates therapeutic use, Hepatitis C drug therapy, Heterocyclic Compounds, 4 or More Rings therapeutic use, Sofosbuvir therapeutic use
Abstract

Background: In both Russia and Sweden, the dominant hepatitis C virus (HCV) is genotype 1, but around one-third of patients have genotype 3 infection. For such countries, HCV genotype testing is recommended prior to therapy. An effective pangenotypic therapy may potentially eliminate the need for genotyping. In this study, we evaluated the efficacy and safety of sofosbuvir/velpatasvir for 12 weeks in patients from Russia and Sweden., Methods: In an open-label, single-arm phase-3 study, patients could have HCV genotype 1-6 infection and were treatment-naïve or interferon treatment-experienced. All patients received sofosbuvir/velpatasvir, once daily for 12 weeks. The primary endpoint was sustained virologic response 12 weeks post-treatment (SVR12)., Results: Of 122 patients screened, 119 were enrolled and treated. Overall, half (50%) were male, 18% had cirrhosis, and 24% had failed prior interferon-based therapy. In total, 66% of patients were infected with HCV genotype 1 (59% 1b and 7% 1a), 6% with genotype 2, and 29% with genotype 3. The overall SVR12 rate was 99% (118/119, 95% confidence interval 95-100%). One treatment-experienced patient infected with HCV genotype 3 experienced virologic relapse after completing treatment. The most common adverse events were headache (16%) and fatigue (7%). Serious adverse events were observed in four patients, but none were related to treatment. No patients discontinued treatment due to adverse events., Conclusion: Sofosbuvir/velpatasvir as a pangenotypic treatment for 12 weeks was highly effective in patients from Russia and Sweden infected with HCV genotypes 1, 2, or 3. Sofosbuvir/velpatasvir was safe and well-tolerated. Clinical trial number: ClinicalTrials.gov NCT02722837.

Published
2019
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16. [Heptral potentialities in the treatment of hepatic damage in children with malignant blood disease].

Author

Reĭzis AR and Nurmukhametova EA

Subjects
Adolescent, Antineoplastic Agents adverse effects, Biomarkers blood, Child, Child, Preschool, Drug Administration Routes, Follow-Up Studies, Hematologic Neoplasms drug therapy, Hematologic Neoplasms enzymology, Humans, Liver Diseases complications, Liver Diseases enzymology, Male, Retrospective Studies, S-Adenosylmethionine administration & dosage, Alanine Transaminase blood, Aspartate Aminotransferases blood, Hematologic Neoplasms complications, Liver Diseases drug therapy, S-Adenosylmethionine therapeutic use
Abstract

Aim: To assess benefit for children with malignant blood disease (MBD) of the hepatoprotector heptral., Materials and Methods: 67 children with blood malignancy aged 3-14 years were examined (53 of them had acute lymphoblastic leukemia). 39 patients were in the study group (25 of them had hepatitis B or C), 28 were controls. Initially, heptral was injected intravenously (14 days) then orally (16-30 days). Activity of transaminases and number of violations of polychemotherapy protocols because of hepatic toxicity were registered., Results: Heptral administration led to inhibited activity of AlAT and AsAT especially in non-infected patients. Protocol deviations became less frequent., Conclusion: Heptral is a potent hepatoprotector in hepatic lesions of toxic, viral and mixed origin.

Published
1998

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