Abstract

Background: Hepatitis C virus (HCV) infection is a known underlying factor contributing to hepatocellular carcinogenesis. The use of direct-acting antiviral (DAA) medication is a form of clinical management for controlling HCV infection and reducing the hepatocellular carcinoma incidence. This medication is introduced to several endemic areas. The big concern is on the treatment expenditures. Several alternative options are proposed and it is required to assess the effect of each alternative option. Objective: Here, the authors assessed and estimated the required treatment expenditures for HCV infection and advantage in the reduction of hepatocellular carcinoma incidence based on the analysis of possible options in an endemic area. Methods: A medical economics analysis was done. Results: According to the cost–utility analysis, the best alternative option that is hereby recommended is DAA medication coverage for all cases. Conclusion: DAA medication coverage for all cases is recommended.

Introduction

Hepatitis C infection is a known underlying factor contributing to hepatocellular carcinogenesis. The use of direct-acting antiviral (DAA) medication is a form of clinical management for controlling hepatitis C virus (HCV) infection and reducing the hepatocellular carcinoma incidence.[1] This medication is introduced to several endemic areas with a hope that it can help better control and eradicate diseases.[2] Roche et al. concluded that it is essential to study the effectiveness of DAA medication for the conclusion of the advantage.[3]

In Thailand, HCV infection is also very common. The use of DAA medication is the new public health strategy to counteract HCV infection and its complications.[4] [5] [6] Poovorawan et al. proposed a dramatical decrease of HCV infection and its complications including hepatocellular carcinoma within a 20-year period of implementation of DAA medication.[5] The huge concern is on the treatment expenditures. Several alternative options are proposed and it is required to assess the effect of each alternative option. Here, the authors assess and estimate the required treatment expenditures for HCV infection and advantages in the reduction of hepatocellular carcinoma incidence based on an analysis of possible options in an endemic area.

Materials and Methods

The main aim of this study is to estimate the required treatment expenditures for HCV infection and advantages in the reduction of hepatocellular carcinoma incidence based on an analysis of possible options in an endemic area, Thailand. The basic data on expenditure required for DAA medication in the setting are referred to a previous nationwide study.[4] The estimation of required expenditures is done according to the path probability of each possible option to expand the coverage of DAAs as follows: (a) coverage for all cases, (b) expanded selective coverage for cases with fibrosis in the range of F2–F4 which is the present strategy in the study setting, (c) doubling the number of DAA treatments plus coverage for all cases, and (d) doubling the number of DAA treatments plus selective coverage expanded selective coverage for cases with fibrosis in the range of F2–F4. The advantage in each alternative option is also estimated and is defined as the expected reduction rate of HCV-related hepatocellular carcinoma incidence with reference to the previous reports by Wasitthankasem et al.[4] for general local population and Duberg et al.[5] for increasing the effectiveness of doubling DAA medication. Cost–utility analysis is further performed comparing each alternative option.

Results

According to this study, the expected required expenditure and advantage in each alternative option for DAA medication is shown in [Table 1]. According to the results obtained from the cost–utility analysis [Table 2], the best alternative option recommended is the DAA medication coverage for all cases.

Table 1 The expected required expenditure and advantage in each alternative option for direct-acting antiviral medications

Table 2 Cost-utility analysis for each alternative option for direct-acting antiviral medications

Discussion

The use of DAA medication is the hope for successful management of HCV infection and HCV-related disease including hepatocellular carcinoma. The eradication of the disease is usually mentioned. Nevertheless, the huge obstacle for achieving the target is the expenditure for medication. In Thailand, HCV infection is not uncommon and is an important contributing cause of hepatocellular carcinoma. The introduction of DAA medication becomes the new public health strategy in the control of HCV infection and hepatocellular carcinoma in Thailand.[4] Due to the high expenditure, the proposal for reducing the cost of DAAs is raised and expected to be the way to reach the success in HCV elimination.[4]

Based on the present study, it can be confirmed that there is a possibility that HCV eradication and control of HCV-related hepatocellular carcinoma are possible in Thailand. The use of coverage for all cases plus doubling DAA medication is the alternative option that can help achieve that target. Nevertheless, the expenditure is still the huge consideration. Chhatwal et al. noted that there was a requirement for analysis of the real situation in the developing countries in endemic areas, which could reflect the real advantage of implementation of DAA medication.[7] According to the present cost–utility analysis, the presently used strategies, expanded selective coverage for cases with fibrosis in the range of F2–F4, is not the most appropriate alternative. The best alternative option that is hereby recommended is DAA medication coverage for all cases.

Conclusion

In this work, a medical economic analysis was done to find the most appropriate option for HCV treatment with aim at reduction of hepatocellular carcinoma. According to the present medical economics analysis, the DAA medication coverage for all cases is the most preferable option.

Conflict of Interest

There are no conflicts of interest.

• References

• 1 Puchades Renau L, Berenguer M. Introduction to hepatitis C virus infection: Overview and history of hepatitis C virus therapies. Hemodial Int 2018; 22 (01) Suppl S8-21
• 2 Braillon A. Direct-acting antiviral drugs and hepatitis C virus: A therapeutic revolution?. Cancer 2015; 121: 4268-9
• 3 Roche B, Coilly A, Duclos-Vallee JC, Samuel D. The impact of treatment of hepatitis C with DAAs on the occurrence of HCC. Liver Int 2018; 38 (01) Suppl 139-45
• 4 Wasitthankasem R, Vichaiwattana P, Siripon N, Posuwan N, Auphimai C, Klinfueng S. et al. Liver disease burden and required treatment expenditures for hepatitis C virus (HCV) infection in Thailand: Implications for HCV elimination in the new therapeutic era, a population-based study. PLoS One 2018; 13: e0196301
• 5 Poovorawan K, Pan-Ngum W, White LJ, Soonthornworasiri N, Wilairatana P, Wasitthankasem R. et al. Estimating the impact of expanding treatment coverage and allocation strategies for chronic hepatitis C in a direct antiviral agent era. PLoS One 2016; 11: e0163095
• 6 Duberg AS, Blach S, Falconer K, Kåberg M, Razavi H, Aleman S. et al. The future disease burden of hepatitis C virus infection in Sweden and the impact of different treatment strategies. Scand J Gastroenterol 2015; 50: 233-44
• 7 Chhatwal J, He T, Lopez-Olivo MA. Systematic review of modelling approaches for the cost effectiveness of hepatitis C treatment with direct-acting antivirals. Pharmacoeconomics 2016; 34: 551-67

• Address for correspondence

  Dr. Beuy Joob
  Sanitation 1 Medical Academic Center
  Bangkok
  Thailand   
  Email: beuyjoob@hotmail.com
  
  

  Publication History

  Received: 02 May 2018
  
  Accepted: 21 May 2018
  
  Article published online:
  03 June 2021
  

  © 2020. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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• References

• 1 Puchades Renau L, Berenguer M. Introduction to hepatitis C virus infection: Overview and history of hepatitis C virus therapies. Hemodial Int 2018; 22 (01) Suppl S8-21
• 2 Braillon A. Direct-acting antiviral drugs and hepatitis C virus: A therapeutic revolution?. Cancer 2015; 121: 4268-9
• 3 Roche B, Coilly A, Duclos-Vallee JC, Samuel D. The impact of treatment of hepatitis C with DAAs on the occurrence of HCC. Liver Int 2018; 38 (01) Suppl 139-45
• 4 Wasitthankasem R, Vichaiwattana P, Siripon N, Posuwan N, Auphimai C, Klinfueng S. et al. Liver disease burden and required treatment expenditures for hepatitis C virus (HCV) infection in Thailand: Implications for HCV elimination in the new therapeutic era, a population-based study. PLoS One 2018; 13: e0196301
• 5 Poovorawan K, Pan-Ngum W, White LJ, Soonthornworasiri N, Wilairatana P, Wasitthankasem R. et al. Estimating the impact of expanding treatment coverage and allocation strategies for chronic hepatitis C in a direct antiviral agent era. PLoS One 2016; 11: e0163095
• 6 Duberg AS, Blach S, Falconer K, Kåberg M, Razavi H, Aleman S. et al. The future disease burden of hepatitis C virus infection in Sweden and the impact of different treatment strategies. Scand J Gastroenterol 2015; 50: 233-44
• 7 Chhatwal J, He T, Lopez-Olivo MA. Systematic review of modelling approaches for the cost effectiveness of hepatitis C treatment with direct-acting antivirals. Pharmacoeconomics 2016; 34: 551-67