A Cost-Utility Analysis of Different Antiviral Medicine Regimens in Patients With Chronic Hepatitis C Virus Genotype 1 Infection.

BACKGROUND: Despite the introduction of new drug regimens with high effectiveness for the hepatitis C virus (HCV) patients, especially in HCV genotype 1, no cost-effectiveness study on the selection of the superior drug strategy in Iran has been conducted yet.
OBJECTIVES: This study is aimed to assess the cost-effectiveness of the three drug regimens of pegylated interferon and ribavirin (PR), sofosbuvir (SOF) + PR and ledipasvir and sofosbuvir (LDV/SOF) in patients with HCV genotype 1 in Iran in the year 2014.
METHODS: A Markov micro-simulation model was used to evaluate the cost-effectiveness of the three drug strategies for a cohort of 10000 patients. Quality-adjusted life-years (QALYs) were extracted from published studies. Cost data was estimated through the review of medical records and obtaining experts opinion.
RESULTS: The results showed that the SOF + PR drug compared with PR had a lower cost and was more effective, but compared with the LDV/SOF, in spite of its lower cost, it was less efficient. The QALY values obtained for PR, SOF + PR and LDV/SOF, respectively, were 10.98, 12.08 and 12.28 and their costs were $ 41,741, $ 7,676 and $ 46,993. Moreover, the results obtained from acceptability curves showed that SOF + PR were the most cost-effective treatment for thresholds below $ 45,270 PPP.
CONCLUSIONS: The use of SOF + PR regimen or LDV/SOF can significantly reduce the incidence of complications associated with the disease. For example, short and long-term outcomes are better than the current drug regimens for HCV genotype 1 patients in all stages of the disease.

1. Background

Hepatitis C can incessantly have a substantial impact on the health system with an increasing burden being expected in the next decade due to related mortality, morbidity, and liver transplantation (1). Early treatments of chronic HCV can considerably decrease the risk of developing advanced liver disease such as cirrhosis and liver cancer, decrease mortality and thus reduce the related costs (2-4).

Treatment of chronic HCV infection, with PR as the previous standard of care, is lengthy (24 to 48 weeks) and toxic with moderate efficacy. This treatment can result in sustained virological response (SVR) in about 80% of people with genotypes 2 and 3 and about 40% - 50% of people with genotype 1 (5, 6).

However, the treatment of chronic HCV infection is rapidly improving (7-11). The new regimens are highly efficacious (> 90% SVR), have reduced the duration of treatment (8 to 12 weeks) and have minimal side effects (12), which resulted in improving the patients’ quality of life (6). The high price of the new regimens is the main factor limiting their use in many countries.

It is estimated that about 187,000 people with chronic HCV infection live in Iran with more than 50% of them being infected with genotype 1 (13).

Since SOF is a new drug, there are not many economic evaluation studies on the drug throughout the world. However, the results of a few conducted studies suggests that compared with current treatments for HCV genotype 1, the SOF + PR or LDV/SOF drug regimens can be associated with more favorable short-term and long-term health and economic outcomes at all levels and stages of the disease and they can be considered as a more cost effective option, especially for genotype 1 (14, 15). Several economic evaluation studies on the treatment of CHC have been conducted and published in America and Europe. However, in the Eastern Mediterranean region (EMRO), particularly Iran, there is no published study using economic evaluation models for the study of drug therapy protocols in patients with hepatitis C. Thus, because of the lower rate of improvement in patients with HCV genotype 1, it is necessary to carry out an economic evaluation study to determine the most cost effective strategy amongst the three strategies of PR, SOF+ PR and SOF/LDV. Therefore, this study is aimed to assess the cost-utility of patients with HCV genotype 1 from the perspective of payers and determine the most appropriate drug treatment protocols for this group of patients with regards to cost-utility and economic considerations in the country.

2. Objectives

This study is aimed to assess the cost-effectiveness of three drug regimens of pegylated interferon and ribavirin (PR), sofosbuvir (SOF) + PR and ledipasvir and sofosbuvir (LDV/SOF) in patients with HCV genotype 1 in Iran in the year 2014.

3. Methods

3.1. Model Overview

In this study, we conducted a cost-utility analysis of three drug therapy strategies including PR, SOF + PR and SOF/LDV, which are used for patients with HCV genotype 1. Due to the chronic and recursive nature of HCV infection, the analysis was carried out using the Markov model. The outcome used in this model included QALYs, the costs spent on each health state and each treatment strategy. The scope of the study was the payer; therefore, direct medical and non-medical costs were investigated. The time horizon of the study was the patients’ lifetime and the time interval was one year. For every one year time interval in the model the patients remained at their current state or moved to other health states such as SVR with compensated cirrhosis, SVR without CC, compensated cirrhosis (CC), decompensated cirrhosis (DC), hepatocellular carcinoma (HCC), liver transplant and death. For the nature of changes in disease states to be consistent with other published cost-utility studies (14-17) and to follow the opinions of experts, the time interval was selected to be one-year cycle. Since the time horizon was more than one year, the economic and clinical outcomes were discounted with an annual rate of 7.2% (18) and 3% (19, 20). The mentioned discount rates have been previously used by other published economic evaluation studies in Iran (20). The analysis was carried out using Tree Age 2011 software.

3.2. Patient Population

Because of the lack of evidence in the country regarding the two regimens SOF+PR and SOF/LDV, we used information including effectiveness and transition probability taken from studies published in other countries. However, data on patients using PR was collected from 144 profiles registered by the research center of gastroenterology and hepatology in Baqiyatallah University. Approximately 78% of these patients did not have cirrhosis (score F0- F3) and 22% did (score F4) all with a mean age of 50 years. This is consistent with the reported proportion of HCV patients with cirrhosis in Iran, which is approximately 20% (21). These centers are national referral centers and patients from all over the country are admitted to there for treatment. Micro-simulation analysis was carried out for a cohort hypothetical population of 10000 people.

Patients who were infected with CHC and diagnosed by biopsy or Fibro Sca were entered into the study.

3.3. Switching Drugs

In this study, if patients had no response, showed drug resistance or showed side effects due to initial drug therapy regimens their drugs were switched. Nowadays, combinations of PR regimens are used for treating patients with HCV genotype 1. According to the published studies, in this group of patients, the response rate to this drug regimen is only 40% - 50% (5, 22), which requires the patients who do not respond to the treatment to use a new drug regimen. Recently, two drug regimens, i.e. SOF + PR and SOF/LDV, have been introduced in the country and according to the published evidence the response rate for these drugs in patients with HCV genotype 1 is more than 90% (23, 24). Therefore, for patients who had no response to the current treatment regimen, a switch to a new drug regimen was used and a new state called withdrawal was added to the model.

3.4. Model Structure

Figure 1 shows a schematic diagram of the Markov model for a simulated population of 10000 CHC patients. As indicated by the diagram, CHC patients who are taking the drug can undergo a transition in a reciprocating state. The intended states and their changes were determined and utilized based on the evidence found in the published studies and the opinions of experts. Patients with different health states and are undergoing treatment can face HCC and death. Those with chronic hepatitis C infection were entered into the Markov model as the initial distribution.

Figure 1.

Decision Analysis Model to Evaluate the Cost-Effectiveness of Treatment Strategies for Chronic HCV Patients

CHC, chronic hepatitis C; CC, compensated cirrhosis; DC, decompensated cirrhosis; HCC, hepatocellular carcinoma; SVR, sustained virological response; LT, liver transplantation; W, withdrawal.

The designed Markov model compared the three drug therapy strategies and the patients who were evaluated by the model received one of the three drug regimens (see Figure 1).

3.5. Model Assumptions

- According to the available clinical evidence, the response rate for SOF + PR and SOF/LDV is assumed to be 100%.

- The SVR state in the model is assumed as the goal of treatment and as the cure state.

- It is assumed that patients who reach the SVR state in METAVIR fibrosis score F0 - F2 are left in this state and do not experience the progress of the disease until death.

- It is assumed that patients who reach the SVR state in METAVIR fibrosis score F3 - F4 are possibly less exposed to the risk of developing liver disease than those who do not reach SVR state.

- It is assumed that patients who do not reach the SVR state are at risk of the progress of liver disease.

- The probabilities for some transitions were only available for some drugs. In such cases, regardless of the drug, it was assumed that all treated patients had equal chances of improvement or progression of the disease.

3.6. Transitional Probabilities

Transitional probabilities of parameters used in the model are presented in Table 1. Due to the lack of evidence in the country, especially clinical data about the new drug regimens administered for patients with chronic hepatitis C, most of the transitional probabilities of different health states were extracted from the published studies which were solely focusing on this issue (4, 25-32).

Table 1.

Input Parameters Used in Economic Model: HCV

Variable	Mean	Distribution	SD	Alpha	Beta
Prob CHC to W_pr	0.55	Beta	0.2258	2.67	2.18
Prob CHC to SVR_pr	0.45	Beta	0.2258	2.18	2.67
Prob CHC to CC	0.115	Beta	0.04106	6.94	53.43
Prob CHC to HCC	0.011	Beta	0.04106	0.07	6.38
Prob CC to W_pr	0.55	Beta	0.23868	2.39	1.96
Prob CC to SVR_pr	0.33	Beta	0.23868	1.28	2.60
Prob CC to DC	0.039	Beta	0.04106	0.87	21.36
Prob CC to HCC	0.024	Beta	0.04106	0.33	13.56
Prob DC to LT	0.031	Beta	0.04106	0.55	17.27
Prob LT to Death	0.107	Beta	0.04106	6.06	50.61
Prob DC to HCC	0.014	Beta	0.04106	0.11	8.07
Prob CHC to SVR_ls	0.977	Beta	0.2258	0.43	0.01
Prob CC to SVR_ls	0.96	Beta	0.23868	0.65	0.03
Prob CHC to SVR_spr	0.91	Beta	0.2258	1.46	0.14
Prob CC to SVR_spr	0.79	Beta	0.23868	2.30	0.61
Utility CHC_pr	0.6657	Beta	0.085	20.50	10.30
Utility CHC_spr	0.645	Beta	0.085	20.44	11.25
Utility CHC_sl	0.835	Beta	0.085	15.92	3.15
Utility CC_pr	0.6257	Beta	0.085	20.28	12.13
Utility CC_spr	0.605	Beta	0.085	20.01	13.07
Utility CC_sl	0.795	Beta	0.085	17.93	4.62
Utility DC	0.525	Beta	0.08957	16.32	14.76
Utility DC_spr	0.525	Beta	0.08957	16.32	14.76
Utility DC_sl	0.715	Beta	0.08957	18.16	7.24
Utility HCC	0.465	Beta	0.08957	14.42	16.59
Utility HCC_spr	0.465	Beta	0.08957	14.42	16.59
Utility HCC_sl	0.655	Beta	0.08957	18.45	9.72
Cost CHC_sl	86208	Gamma	34152	6.37	0.00
Cost CHC_spr	11903	Gamma	34152	0.12	0.00
Cost CHC_pr	15772	Gamma	34152	0.21	0.00
Cost CC_sl	86664	Gamma	34035	6.48	0.00
Cost CC_spr	12359	Gamma	34035	0.13	0.00
Cost CC_pr	16771	Gamma	34035	0.24	0.00
Cost DC_sl	101124	Gamma	33796	8.95	0.00
Cost DC_spr	36862	Gamma	33796	1.19	0.00
Cost DC_pr	23798	Gamma	33796	0.50	0.00
Cost HCC_sl	112023	Gamma	31208	12.88	0.00
Cost HCC_spr	52508	Gamma	31208	2.83	0.00
Cost HCC_pr	40718	Gamma	31208	1.70	0.00
Prob HCC to LT	0.0003	Beta	0.04106	0.00	0.18
Prob CHC to SVR_pr_spr	0.72	Beta	0.2258	2.85	1.11
Prob CC to SVR_pr_spr	0.62	Beta	0.23868	2.56	1.57
Prob CHC to SVR_pr_ls	0.79	Beta	0.2258	2.57	0.68
Prob CC to SVR_pr_ls	0.8	Beta	0.23868	2.25	0.56

Abbreviations: Prob, probability; CC, compensated cirrhosis; DC, decompensated cirrhosis; HCC, hepatocellular carcinoma; SVR, sustained virological response; LT, liver transplantation; W, withdrawal; pr, pegylated interferon and ribavirin; spr, sofosbuvir + pegylated interferon and ribavirin; sl, ledipasvir and sofosbuvir; SD, standard deviation, Alpha and Beta are the distribution kind of mentioned variables.

To include the cause of death other than HCV, we used the probabilities of life tabulation 2012 by age and sex. The probabilities of HCV related deaths were extracted from the published studies (4, 14, 15, 25-32). Some other probabilities were also extracted through assessing the registry of patients in the studied centers.

As a number of articles had reported the data on clinical efficacy by rate, we first changed the rates into probabilities using the following formula (33) and then included them in the model.

Equation 1.

Where P, probability; r, rate; t, time.

3.7. Health Outcomes

In this study, QALY was considered as the health outcome. The utility values used in the model are presented in Table 1. Since the two drug regimens of SOF + PR and SOF/LDV are recently introduced and used in the country, there is a lack of sufficient evidence determining the values used in the model, we used the evidence found in studies published in other countries (14-17, 34).

3.8. Cost Inputs

The data on direct medical costs on different states of CHC and other complications associated with the disease such as CC, DC and HCC were extracted from outpatient and inpatient medical records in the mentioned treatment centers and the self-reports of specialists. For each disease state there was an attempt to collect data on direct medical costs including the average number of physician visits, prescribed medicines, diagnostic services, treatment and hospitalization and use of other services.

Resources used to calculate the costs were based on prices from 2014. To make international comparisons we tried to convert the costs to international dollars using the purchasing power parity (PPP) with an exchange rate of 8565.41 Rials per $ 1 (35). The cost of each health state is presented separately in Table 1 with the cost details shown in Table 2.

Table 2.

Results of Drug Acquisition Costs Used in the Model

Treatment	Unit cost, PPP $ ( Per pill)
Ribavirin	0.7
Pegylated interferon	173
Sofosbuvir	60
Ledipasvir/sofosbuvir	979

3.9. Cost-Effectiveness Analysis

Based on the results obtained from the previous stages, a Markov model was applied using the Tree age software and the collected data was included into the model. Taking into account the time horizon of the study, we calculated the costs, effectiveness and cost-effectiveness for all interventions with monetary units. QALY, Cost per QALY and their ICERs were obtained using the following formula (36).

Where A, SOF/LDV; B, other antiviral.

3.10. Sensitivity Analysis

To measure the level of certainty in base-case results, a probabilistic sensitivity analysis (PSA) was performed on the results of the model. Therefore, with regards to the defined probability distributions for the parameters that were entered into the model, a second-order Monte Carlo simulation model was conducted using 5000 trials to analyze the probabilistic sensitivity. PSA results are presented using the cost-effectiveness acceptability curves and incremental cost-effectiveness scatter plot. In this article, the PSA results are characterized with the use of incremental cost-effectiveness, scatter plot and cost-effectiveness acceptability curves. Due to the lack of WTP threshold in Iran the WTP per every QALY, based on the WHO’s approach was considered as one to three times of gross domestic product per capita. In 2014, it was 4670 dollars per capita (37). Meanwhile, due to international comparison, we used the latest gross domestic product per capita based on the purchasing power parity (PPP), which was 15090.05 US dollars in 2013 (37, 38).

4. Results

In this study, based on the initial distribution of the model, a total of 144 CHC patients who were 14 years of age and were referred to the selected centers were enrolled in the study and were classified by age, sex and duration of the disease. The mean age of the patients was 50 years; with 79% being male and 21% female.

The results showed that SOF + PR drug, compared with the two drug therapy strategies, was more cost effective. When compared to the PR it had a lower cost and was more effective but compared with the LDV/SOF, in spite of its lower cost, it was less efficient. As a whole, of the three above-mentioned strategies, SOF + PR was the most cost effective strategy with the next being LDV/SOF. PR drug, which had the highest cost and was less effective than the other strategies, was the failed strategy (see Figure 2, Table 3).

Figure 2.

Comparison of Cost-Effectiveness of the Three Drug Strategies in Patients With Chronic Hepatitis C Based on the Number of QALY

Peg-IFN/RBV, pegylated interferon/ribavirin; SOF + Peg-IFN/RBV, sofosbuvir + pegylated interferon/ribavirin; SOF + LDV: ledipasvir + sofosbuvir; QALY, quality-adjusted life-year.

Table 3.

The Results of a Markov Micro-Simulation Model to Compare the Cost-Effectiveness of the Three Drug Strategies in Patients with CHC Based on the Number QALY (USD)

Strategy	Cost	Eff (QALY)	Inc Cost	Inc Eff	Inc CE	Rank	Subset
SOF + PR	7,676	12.08	0	0	0	1	Dominant
SOF + LDV	46,993	12.28	39,316	0.21	190335	2	Dominant
PR	41,741	10.98	34,064	-1.10	-30985	3	abs. dominated

Abbreviations: Eff, Effectiveness; Inc, incremental cost; Inc Eff, incremental effectiveness, Inc CE, incremental cost-effectiveness; PR, pegylated interferon/ribavirin; SOF + PR, sofosbuvir + pegylated interferon/ribavirin; SOF + LDV, ledipasvir + sofosbuvir; CHC, chronic hepatitis C; QALY, quality-adjusted life-year.

Cost, effectiveness, incremental costs, incremental effectiveness, ICER as well as ratings were the superiority of the three drug strategies in CHC patients. The comparison is presented in Table 3. The findings shown in the tabulation indicate that the QALYs for each of the three medicines of PR, SOF + PR, LDV/SOF were 10.98, 12.08 and 12.28; in addition, the costs were $ 41.741, $ 7.676 and $ 46.993 As shown and compared with other alternatives, PR and LDV/SOF had the minimum and maximum expected effectiveness and SOF + PR and LDV/SOF had the minimum and maximum expected costs over the period of a life time. Furthermore, LDV/SOF with about 190,335 dollars PPP is the highest cost per QALY compared with the other strategies (Table 3).

4.1. Probabilistic Sensitivity Analysis (PSA)

In this study, because it was possible to measure all the variables, they were considered to be distributed. In this study, the distribution of beta (β) was used to determine the distribution of transitional probabilities and utility values that were between 0 to 1. Additionally the gamma distribution was used to determine the distribution of the costs (Table 1). Thus, a second-order Monte Carlo simulation using 5000 trials was conducted for the analysis of probabilistic sensitivity. The results of the measurement of uncertainty using cost-effectiveness acceptability curves and incremental cost-effectiveness scatter plot (ICER) distribution curves are as follows.

The results of the acceptability curves showed that in 91.7% to 85.7% of simulations SOF + PR was the most cost effective treatment for thresholds less than 45,270 US dollars. The next best drug strategy was LDV/SOF which was the optimal strategy in 4.4% to 12.5% of the simulations. PR drug was the best strategy only in 3.9% to 1.8% of the simulations (see Figure 3). Moreover, the results of the bar graph showed that in 85.7% of simulations SOF + PR drug in thresholds less than $ 45,270 was identified as the best strategy while the other strategies were superior strategies only in 14.3% of simulations (see Figure 4A - 4B).

Figure 3.

Cost-Effectiveness Acceptability Curve Obtained Through Monte Carlo Simulation

Peg-IFN/RBV, pegylated interferon/ribavirin; SOF + Peg-IFN/RBV, sofosbuvir + pegylated interferon / ribavirin; SOF + LDV, ledipasvir + sofosbuvir.

Figure 4.

A, B, Scatter Plot of Incremental Cost-Effectiveness of SOF+PR and SOF+LDV Compared with PR

Peg-IFN/RBV, pegylated interferon/ribavirin; SOF + Peg-IFN/RBV, sofosbuvir + pegylated interferon/ribavirin; SOF+LDV, ledipasvir + sofosbuvir.

The scatter plots provide more detailed information for individual comparisons. The results of scatter plots are only shown for the two superior options compared with PR. The results of the scatter plots showed that in 92% and 32% of simulations, respectively, SOF + PR and LDV/SOF, were located in the fourth region of the cost-effectiveness plot. For example in a region with lower-costs and higher effectiveness, as compared with PR, they were considered as the superior strategies. In 2% and 58% of simulations, they were in the first region, under the threshold. For example in a region with higher costs and higher effectiveness, compared with the PR. In 2% and 0% of the simulations they were under the threshold at the third region. Therefore, overall SOF + PR and LDV/SOF in 96% and 90% of simulations were at the acceptable region, below the threshold, as compared with the PR and as a result they defeated the PR strategy and were identified as the more cost effective strategies. Moreover, SOF + PR and LDV/SOF in 4% and 10% of the simulations were in the rejected area above the threshold as compared with the PR and were identified as the non-cost effective (inferior) strategies.

Therefore, the results of sensitivity analysis showed that SOF + PR was the most effective treatment and LDV/SOF was the subsequent treatment strategy with no change in their status compared with the PR strategy. This indicates that the results of this study are robust.

The results also showed that given the better effectiveness of LDV/SOF drug strategy, if the price of the drug decreases from its current price, i.e. from around 980 dollars PPP to 120 dollars PPP per each pill, then it will become the most cost effective strategy and LDV/SOF drug will become dominant and the other two drug strategies of SOF + PR and PR will be totally dominated (see Figure 5). As the results of acceptability curves obtained from the sensitivity analysis showed, in 50% to 89.7% of simulations, LDV/SOF was the most cost effective treatment for thresholds between 4527 to 45270 dollars PPP. SOF + PR drug was optimal only when it was below the threshold of 4527 dollars PPP (see Figure 6).

Figure 5.

Comparison of Cost-Effectiveness of the Three Drug Strategies in Patients With Chronic Hepatitis C Based on the Number of QALY

Peg-IFN/RBV, pegylated interferon/ribavirin; SOF + Peg-IFN/RBV, sofosbuvir + pegylated interferon/ribavirin; SOF + LDV, ledipasvir + sofosbuvir; QALY, quality-adjusted life-year.

Figure 6.

Cost-Effectiveness Acceptability Curve Obtained Through Monte Carlo Simulation

Peg-IFN/RBV, pegylated interferon/ribavirin; SOF + Peg-IFN/RBV, sofosbuvir + pegylated interferon/ribavirin; SOF + LDV, ledipasvir + sofosbuvir.

5. Discussion

Since LDV/SOF medicine is a new drug, there are a limited number of economic evaluation studies published in the world on the drug. Hence, this study was the first economic evaluation research on hepatitis C patients in the country and in the EMRO region. Furthermore, it was one of the very few studies conducted in the world, which tried to take a pharmacoeconomic view to assess the three different drug therapy options for patients with HCV genotype 1. Therefore, this study was carried out to fulfill one of the goals of policy decision makers to select the best drug strategies for the inclusion in the Iran drug list (IDL). In this study, based on the characteristics of the sample under the study analysis, micro-simulation analysis was conducted on CHC patients in a population of 100 thousand people.

The results showed that compared with other alternatives and considering the given prices, SOF + PR was the most cost-effective strategy. This strategy will have the most favorable health economic outcomes in the future compared with other strategies available for patients with HCV and its related complications. In comparison with the SOF + PR, although LDV/SOF drug regimen has the highest rate of SVR, it is not a treatment priority due to its very high price in the country. Therefore, under a fixed budget, more patients can successfully be treated by the SOF + PR drug regimen as compared with other treatment alternatives. In view of that, the results of this study are in line with those of Saab et al.’s study (15). Therefore, SOF + PR has a lower cost and is more effective than PR. Our results are consistent with the findings of the recently published studies, indicating that the SOF drug regimen, compared with the other current standard drug regimens, is more effective for the treatment of HCV genotype 1 (14, 15). Also, the results of the probability sensitivity analysis showed that the SOF + PR drug regimen, compared with the two other medication strategies was more cost effective and in most simulations the obtained values were at the accepted area and below the threshold; thus, it obtained the best results with respect to the given prices. Therefore, the results showed that the sensitivity analysis did not change the status of SOF + PR as the most effective drug regimen; this indicates that the results of this study are robust. Accordingly, the results of this study are in line with those of Saab et al.’s study in the USA and Petta et al.’s study in Italy (15, 16).

The second generation of direct-acting anti-viral drugs (all-oral) such as LDV/SOF has a high efficacy and safety. It is also a simple treatment strategy that is free of PR and makes great progress in improving the patients during treatment and significantly increases SVR rate (39-41). Therefore, the results showed that if the price of this drug reduces, it will be the most cost effective strategy and completely dominates the other two drug regimens of SOF+PR and PR. As the results of acceptability curves are obtained from the sensitivity analysis indicated, LDV/SOF with its new prices could be the most cost effective treatment in 89.7% of simulations for thresholds below 45270 dollars PPP.

Thus, our results showed that SOF + PR or LDV/SOF drug regimens could be associated with more favorable short and long term health economic outcomes, as compared with the current treatments for patients with HCV genotype 1 at all levels and stages of the disease. It can be a more cost effective option, especially for genotype 1.

Therefore, in order to increase the rate of SVR, reduce the treatment period, increase the quality of life of patients and increase productivity during and after the treatment period on one hand and to significantly reduce the risk of complications associated with liver-disease, mortality and the costs for patients using SOF medication regimens (6, 14, 15, 42) on the other hand, it is recommended to stop the use of the current standard PR treatment regimen in Iran and many other countries, as they are not recommended for treating patients with HCV genotype 1. Therefore, a drug with high efficiency such as SOF should be used along with PR. Furthermore, as mentioned earlier, in the case of decreasing the price of the drug (LDV/SOF), it will be better to use a PR-free drug regimen instead of the SOF + PR combination and use it as a priority for the treatment of patients. This PR-free regimen has shown high clinical efficacy, especially in patients with HCV genotype 1 who form the major number of HCV patients in Iran.

According to our study, to generalize the results to other settings it is better to consider some factors such as the availability of resources, prices, valuing outcomes by individuals, thresholds and other indicators of the effectiveness used in various studies that may affect the results of those studies. Therefore, the generalization of the results to other settings should proceed with caution.

One of the limitations of this study was the use of some data obtained from clinical trial studies which might differ slightly from real-world conditions. Another limitation was the lack of access to patients using SOF regimen, which was due to the high price of the drug in the country. Also, because of the limitations of the data required for some simulations we had to use the constant of transitional probabilities in the model in this study.

In conclusion, based on the findings of this study, it can be concluded that the use of SOf + PR and PR-free drug regimens (LDV/SOF; Harvoni) in patients with HCV genotype 1 can reduce the side effects associated with the disease such as HCC, DC and mortality. Additionally, it can reduce the costs and time spent on the disease, especially if the patient refers at early stages of the disease without cirrhosis and without previous experience of therapy. Even in treatment-experienced and cirrhosis patients, the mentioned treatments are the most cost-effective option in the current situation and can be used as top priority drugs. They can also be used for switching from PR to the mentioned drugs.