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Brazilian Journal of Infectious Diseases

Print version ISSN 1413-8670

Braz J Infect Dis vol.13 no.3 Salvador June 2009 

Cost effectiveness of peginterferon alfa-2B combined with ribavirin for the treatment of chronic hepatitis C in Brazil



Marcelo Cunio Machado FonsecaI; Gabriela Tannus Branco de AraújoI; Denizar Vianna AraújoII

IFederal University of São Paulo; São Paulo, SP, Brazil
IIState University of Rio de Janeiro; Rio de Janeiro, RJ, Brazil

Address for correspondence




The treatment of chronic hepatitis C (CHC) with peginterferon alpha-2b/ribavirin (PegIFN + Rib) produced larger sustained viral response (SVR) compared to the conventional (non-pegylated) interferon/ribavirin (IFN + Rib), but its cost-effectiveness was not assessed in Brazil. We developed a Markov model to mirror the natural disease history and cohorts of patients with hepatitis C virus (HCV), that received PegIFN + Rib or IFN + Rib treatment for 48 or 24 weeks, according to viral genotype and liver histology. The SVRs for the treatments PegIFN + Rib and IFN + Rib were respectively 48% and 34% (genotype 1), and 88% and 80% (genotype non-1). Three Delphi panels were conducted with hepatologists and intensivists, and another one with oncologists. The costs are expressed in 2006 Brazilian Reais (R$) and the benefits were discounted at 3%. In genotype 1 HCV patients, PegIFN + Rib increases the life expectancy (LE) in 0.51 year, and the quality-adjusted life years (QALY) in 0.78, as compared to IFN + Rib. In genotype non-1 HCV patients, PegIFN + Rib increases the LE in 0.29 years and the QALY in 0.44 years, as compared to IFN + Rib. The incremental cost-effectiveness rate, considering all the genotypes, was of R$19,848.34 per QALY. Peginterferon alpha-2b with ribavirin is a cost-effective therapy for the treatment of naïve CHC adult patients compared to the interferon alpha-2b and ribavirin regime, irrespective of the viral genotype.

Key-Words: Hepatitis C, cost-benefit analysis, effectiveness, interferons.



Hepatitis C is an infection generally presenting a slow progression [1], and its occurrence and prevalence within the population was not yet completely elucidated [2].

In a study developed in the city of São Paulo, an estimate prevalence of 1.42% (CI 0.70% - 2.42%) for hepatitis C was found, which, when projected to the entire Brazilian territory, results in a figure between 1.1 and 3.4 million of HCV infected people [2].

Hepatitis C virus (HCV) genotyping is important to define the treatment time: 48 weeks for genotype 1 and 24 weeks for other genotypes. The treatment aim is to achieve a sustained viral response (SVR), which is defined as the absence of detection of serum HCV RNA at the treatment final, and six months later as well; to confirm this condition, an essay with sensitivity of, at least, 100 copies (50 IU) per milliliter was used.

Interferon alpha/ribavirin (IFN + Rib) association has become the treatment gold-standard for C hepatitis from 1998 on [3].

In order to improve the efficacy, side effects profile and the therapeutic scheme itself, pegylated-interferons alpha (PegIFN) have been developed, and are currently considered as the treatment gold-standard for hepatitis C [4].

There are two different products available in the Brazilian market, the peginterferon alpha 2b weighing 12 kD, and the peginterferon alpha 2a weighing 40 KD.

In two multicentric, double-blind, randomized clinical trials using ribavirin in both treatment arms ("IFN" arm and "PegIFN" arm), the global SVR rate achieved by peginterferon alpha 2a was 56% [5], and by peginterferon alpha 2b 54% [6].

The health system is concerned about hepatitis C, because the great period of infection for this disease occurred in the 80's [7], and, taking in account the disease progression [6] and that the therapeutic results are not yet satisfactory, it is expected that the great impact, in terms of number of people carrying the disease as well as the costs involved, will occur in the first two decades of this third millennium.

Due to the clinical course of the infection, it is improper or even feasible to conduct controlled and randomized clinical trials, to investigate the medical-economic impact that better SVR rates could represent [8].

It is unknown whether the short-term costs will be compensated by the possible savings (lesser complications and transplantations) or, even, the extension in which better response rates from pegylated interferons will represent, in terms of life years or quality of life.

As treatment decisions have to be taken right now, we built an analytic decision model to assess both the long-term 'clinical' and 'cost-effectiveness' results that are currently obtained from the treatment of chronic hepatitis C in Brazil, using for this purpose the best available information, although still imperfect [8].


Material and Methods

We built the model using decision analysis techniques [9]. The analysis was developed in a hypothetical cohort of 30 year-old men and women with chronic hepatitis C, settled in the 2006 Brazilian health system. The primary study perspective is that of private medicine (insurances, HMOs, cooperatives, self-managements).

The adopted data sources were the medical literature [6]; published official prices for medications, procedures, and hospital supplies; and Brazilian population statistics.

The determination of actual costs of hepatitis C treatment was performed through a microcosting process based on modified Delphi panels [10].

Values should be divided by 2.18 to convert the economic result to 2006 US dollars.

Markov Model for Chronic Hepatitis C

A Markov model has been developed for the natural history of chronic hepatitis C.

The health status were based on histology, presence or absence of viremia; presence of uncompensated hepatic disease; hepatocellular carcinoma or hepatic transplantation; describing the following conditions: remission, mild hepatitis C, moderate hepatitis C, hepatocarcinoma, cirrhosis or uncompensated cirrhosis, to be submitted to hepatic transplantation, to be transplanted, and death. Due to the large variability in treatment and costs, uncompensated cirrhosis health status, was further split in ascytis, refractory ascytis, hemorrhagic varices and hepatic encephalopathy. The prevalence of genotype 1 in Brazil is 74% [2].

The simulation starts after the diagnose of chronic hepatitis C, and assumes three groups of patients: one treated with conventional IFN, another with PegIFN alpha 2b of 12 kD, and a non-treated group of patients. Every year, the patients transit between the health status categories. The model considers that healed patient will not have hepatitis C recurrence. The analysis compares the evolution of a disease treated with PegIFN alpha 2b of 12 kD given subcutaneously, with a once per week dose of 1.5 mg/kg, associated with oral ribavirin 1000-1200 mg/day (PegIFN + Rib) or, IFN alpha 2b, conventional, non-pegylated, given subcutaneously, with dose of 3 MU three times per week (IFN + Rib), also associated with oral ribavirin 1,000-1,200 mg/day.

Time Window

Due to the slow progression of chronic hepatitis C [8], the base case was analyzed for a life-time period.

Clinical Outcomes

The clinical efficacy outcomes used were global SVR, SVR for genotype 1, and SVR for genotype non-1 [6]. The model made the extrapolation of these efficacy data for effectiveness outcomes: number of life years gained and number of quality-adjusted life years gained.

Delphi Panel

The modified Delphi panels are used in order to obtain data and develop consensus in pharmacoeconomic studies [10]. Two rounds of Delphi panels were developed, always with the same experts, to allow the consensus.

Following categories of professionals were excluded from the panel: physicians that are somehow linked to the pharmaceutical industry, such as speakers, consultants, or employees; or those occupying positions in universities: professors, lecturers, and physicians occupying positions within medical associations: directors, presidents. These professionals were excluded because, as opinion leaders, during the Delphi panel process they could possibly influence the opinion of other professionals.

The modified Delphi panel was developed with six hepatologists; and for the status of hepatocarcinoma and hepatic encephalopathy, with six oncologists and six intensivists, respectively.

The local management for the status of mild and moderate chronic hepatitis C, cirrhosis, ascytis, refractory ascytis, esophageal varices, hepatic encephalopathy, and hepatic transplantation were equal for all the studied schemes.

Microcosting and Costs Determination

Microcosting is the process to identify and measure every resource used, assigning values and integrating such information thereafter. After this process, all values were determined for the administration of each therapeutic scheme as well as their consequences, and costs related to the evolution of the treated hepatitis C with each treatment studied.

Discount Rate

The process of "discounting" assumes that the expended or saved money, and the saved or lost years in the future, do not have the same value as today. This process decreases the future costs and life years (consequences), every year, according to a fixed percentage rate [11].

We used a discount rate of 3% [12]. Sensitivity analyses were developed with discount rates between 0% and 5%.

Cost-Effectiveness Analysis

The cost-effectiveness analysis compares the costs and clinical outcomes linked to effectiveness for different therapeutic alternatives.

The incremental cost-effectiveness rate (ICER) represents the additional cost and effectiveness obtained, when the PegIFN + Rib regime is compared to the IFN + Rib regime.

Quality of Life

There are two studies in which the utilities, for every health states related to chronic hepatitis C, are determined by a panel of hepatologists familiarized with the disease, and the disease treatment with interferon [13,14]. In our study, the utility values for each health states are the same for the PegIFN + Rib arm and IFN + Rib arm. Table 1 presents the costs and utilities per every health status used in the model.

Cost-Utility Threshold

There is not an ICU (Incremental Cost-Utility) threshold in Brazil being considered as ideal for the acceptance of a given health intervention. Therefore, we used the value established by the World Health Organization (WHO), corresponding to three times the per capita gross domestic product (GDP), as a threshold for cost-effectiveness/utility [18,19].

According to the Brazilian Institute of Geography and Statistics (Instituto Brasileiro de Geografia e Estatística - IBGE), the 2006 per capita GDP value is R$12,491.00 [20]. Therefore, if a health procedure presents an ICER lower than R$37,493.00 in Brazil, it may be considered as being cost-effective.

Sensitivity Analysis and Validation

The role of the sensitivity analysis is to test the stability of the results when varying different model parameters. These model parameters are changed, varying their values within a plausible range found in the literature and checking the related effect on the global model outcome. If the global outcome of the strategy under analysis remains stable with the variation of a given parameter value, then the model outcome is insensitive to the variation of this parameter being assessed. The model was recalculated with univariate and bivariate adjustments.

The sensitivity analysis was performed for the following parameters inserted in the model:

- Clinical events: transition probability from mild chronic hepatitis C to remission; from mild chronic hepatitis C to moderate chronic hepatitis C; from moderate chronic hepatitis C to cirrhosis; from moderate chronic hepatitis C to hepatocarcinoma; from cirrhosis to ascytis; from cirrhosis to hemorrhagic varices; from cirrhosis to hepatic encephalopathy; from cirrhosis to hepatocarcinoma; from ascytis to refractory ascytis; from ascytis to death; from refractory ascytis to death; from hemorrhagic varices to death in the first year; from hemorrhagic varices to death in the subsequent years; from hepatic encephalopathy to death in the first year; from hepatic encephalopathy to death in the subsequent years; from hepatocarcinoma to death; from uncompensated cirrhosis to hepatic transplantation; from hepatic transplantation to death in the first year; from hepatic transplantation to death in the subsequent years.

- Economic parameters: cost of mild chronic hepatitis C; moderate chronic hepatitis C; cirrhosis; ascytis; refractory ascytis; hemorrhagic varices; hepatic encephalopathy; hepatocarcinoma; hepatic transplantation; subsequent years to transplantation; mild hepatitis C utility; moderate hepatitis C utility; cirrhosis utility; ascytis utility; refractory ascytis utility; hemorrhagic varices utility; hepatic encephalopathy utility; hepatocarcinoma utility; hepatic transplantation utility; hepatic transplantation utility subsequent years; healed utility; discount rate; price of the drugs used in the treatment.

As uncertainty could occur with any of the model parameters, we performed a Monte Carlo simulation with ten thousand interactions that simultaneously varies all of the above mentioned parameters. In order to check the internal validity of our model, we developed many tests and debugging processes. The external validation was performed comparing the results projected by the model with external epidemiologic data not used in this model [21].

Data Sources

The standard treatment and the health care resource utilization values came from the Delphi panel. The values used for prices assignment are based on public sources.

Initial Parameters and Probabilities

Initial Parameters

The cohorts that passed through the model simulation had a 74% prevalence for genotype 1, and 26% for non-1 genotypes [2].

In the simulation, two cohorts received effective treatment; one of them with conventional IFN alpha 2b, and the other with PegIFN alpha 2b of 12 kD; the third cohort simulated the natural disease evolution, without any treatment.

The average body weight of Brazilian patients receiving treatment for chronic hepatitis C is 76.7 kg and 64.9 kg for male and female patients, respectively [22]; therefore, the ribavirin dose given to these patients is higher than 10.6 mg/kg. Furthermore, we used the response rates being compatible with the higher dose of ribavirin per kilogram [6].

The treatment time was 48 weeks for genotype 1, and 24 weeks for the other genotypes, for both treatment arms.

Genotype 1 patients were submitted to quantification of viral titer by means of a PCR test: after 12 weeks in the cohort with PegIFN alpha 2b, and 24 weeks in the cohort with conventional IFN [23].

Patients not presenting a significant decrease in their individual viral load had their treatments interrupted [5, 22].


The probabilities inherent to the natural history of patients with mild chronic hepatitis C (transition to moderate hepatitis) and moderate CHC (progression to cirrhosis or hepatocarcinoma) were obtained from three retrospective observational studies [24-26]. In patients with mild chronic hepatitis C, the yearly probability of spontaneous disease resolution comes from two studies [27,28].

The progression of patients with compensated cirrhosis (development of hepatocarcinoma and uncompensated cirrhosis) was based on a study from Fattovich et al. [29]. As the literature suggests that mortality due to uncompensated cirrhosis is different, depending on its presentation, we stratified the uncompensated cirrhosis into different categories: ascytis, hemorrhagic varices, hepatic encephalopathy, and ascytis refractory to treatment [8].

In patients with ascytis, after three years of follow-up, Salerno has detected a yearly mortality of 11% and an evolution probability to refractory ascytis of 6.7%; for patients with refractory ascytis, the yearly probability of death increased to 33% [30].

Patients with hemorrhagic esophageal varices had a mortality rate of 40%, in the first year, and of 13% in the three subsequent years of follow-up [31].

For patients presenting hepatic encephalopathy, but without hemorrhagic varices, the mortality rate was 68% in the first year, and 40% in the following years [32].

In relation to hepatocarcinoma, the mortality rate is 86% [33].

A total of 792 hepatic transplantations were conducted in Brazil during 2003 [34]. The overall hepatic transplantation rate was of 4.95 per million, i.e., 33% of the United States rate, where the yearly transplantation rate in patients with hepatitis C is 3.1%. In such a way, we estimate the transplantation probability for hepatitis C patients in Brazil as 1.023% (33% of 3.1%).

The mortality rates for the first post-transplantation year, and for the subsequent years, come from three studies [35-37].

Table 2 shows the annual probabilities of disease progression used in this model.

The model assumes for both therapeutic schemes that, in case of therapeutic failure, the probabilities of disease progression are the same as the natural disease evolution. Therefore, the difference between the treatment study arms are the response rates achieved by the different studied therapeutic regimes.

Other Causes for Mortality

The yearly risk of death was obtained from the Brazilian vital statistics [38].



Effectiveness - Life Years Gained

The model projects a life expectation of 18.71 years for the non-treated patients' cohort. When adjusted for quality of life, it is 16.80 years.

There is a gain of 2.23 years (12%) for patients treated with PegIFN alpha 2b, and of 1.72 (9%) year for those treated with IFN alpha 2b.

In relation to the IFN alpha 2b regime, the PegIFN regime resulted in an increase of 2.5% in the global life expectancy, a life time window.

In patients with genotype 1, PegIFN alpha 2b resulted in an increase of 2.5% in life expectancy.And the life expectancy increase was of 1.3% for non-1 genotype patients, with IFN alpha 2b regime.

Effectiveness - Quality of Life

When the life years gained are adjusted for the quality of life, the model projects better results for the treated populations versus the natural disease evolution.

There are gains of 3.39 years for patients treated with PegIFN alpha 2b (20%), and 2.61 years for patients treated with IFN alpha 2b (15.5%).

The PegIFN alpha 2b regimen resulted in an increase of 4% in quality adjusted life years gained, corresponding to 0.78 quality adjusted life years gained in relation to the IFN alpha 2b regimen.

In the non-1 genotype patients, the treatment with PegIFN alpha 2b resulted in an increase of 2% in the patients' quality adjusted life expectancy, meaning 0.44 quality adjusted life years in an entire life window, in relation to the IFN alpha 2b regime.

Economical Results

The average cost of a patient with chronic hepatitis C along an entire life is R$39,147.32.

Considering the life time window, the average cost discounted by 3%, for the patient who received PegIFN alpha 2b was of R$59,782.93; and for the patient who received IFN alpha 2b was of R$44,334.25.

The costs for the health states of mild chronic hepatitis C and moderate chronic hepatitis C are equal for the three studied cohorts (patients without treatment, being treated with PegIFN alpha 2b or, otherwise, conventional IFN alpha 2b), because none of these patients received treatment yet, and all of them will be treated at the same time, in all cohorts.

The costs related to all health states are constantly higher for non-treated patients, except for mild chronic hepatitis C and moderate chronic hepatitis C.

The patients treated with PegIFN alpha 2b present lower cost in all health states following moderate chronic hepatitis C, irrespective to the viral genotype. The area under the expenses curve in relation to time of the health states of cirrhosis, uncompensated cirrhosis, hepatic transplantation, and hepatic transplantation-subsequent years for IFN alpha 2b is higher than for PegIFN alpha 2b, not only due to the higher costs achieved, but also because these costs remain in such high levels longer than for PegIFN alpha 2b.


In an entire life time window, within the global population, there is a gain of 0.78 quality adjusted with PegIFN alpha 2b compared to IFN alpha 2b, however, there is also an incremental cost of R$15,448.68. Therefore, the point estimate cost-utility of PegIFN alpha 2b in relation to IFN alpha 2b is R$19,848.34. The cost utility rates of PegIFN alpha 2b and IFN alpha 2b in relation to no treatment are R$6,087.20 and R$1,987.33, respectively.

Sensitivity Analysis - Marginal Cost-Utility

In the univariate analysis, the incremental cost-utility varied between R$14,322.93 and R$32,436.38 for each quality adjusted life year gained, after the variation of transition probabilities and costs within the range of plausible values, and increasing or decreasing by 50% the costs of the different health states.

The model was insensitive to all univariate variations of transition probabilities and costs.

In a bivariate analysis, using the clinical and economical parameters with the widest variation, transition probability of mild chronic hepatitis C to remission and discount rate, respectively for the whole population, the incremental cost-utility is sensitive to a discount level of 5%, unless the spontaneous remission is probability higher than 0.001 yearly. This same analysis splitting the population in patients with genotype 1 and non-1 has demonstrated that for genotype 1 patients, the incremental cost-utility is sensitive to a discount level of 5%, unless the spontaneous remission probability is higher than 0.004 yearly. For patients with non-1 genotype virus, the incremental cost-utility was never above R$37,493.00, even when the discount rate was 5%, and the spontaneous remission probability lower than 0.000 yearly.

Monte Carlo Probabilistic Sensitivity Analysis

Within an entire life time window, the mean cost-utility obtained through the Monte Carlo simulation with ten thousand interactions for the whole cohort, for patients with chronic hepatitis C due to genotype 1 virus, and due to genotype non-1 virus was of R$17,774.10, R$16,523.62, and R$12,583.45, respectively.

The outcomes of the Monte Carlo simulation are shown in Figures 1 and 2, in which the cost-utility rate is presented as a function of a threshold rate. This "threshold -rate" is that which a given healthcare decision maker or payer would be willing to pay, to include a given drug into his/her formulary. For genotype 1 CHC patients, the cost-utility rate found in the model (R$23,392.18) presents an acceptance probability around 68%, while 90% of the 10,000 results obtained in the Monte Carlo simulation are below the limit of R$37,493.00 considered, in Brazil, and according to the WHO criteria, as the "threshold -rate" of cost-effectiveness/utility.

For patients with genotype non-1, the cost-utility rate found in the model (R$17,083.54) presents a probability to be accepted around 65%. We also verified that 95% of the 10,000 results obtained in the Monte Carlo simulation are below the limit of R$37,493.00.

Model Validation

The external model validation was performed comparing the cirrhosis development probability, after 20 years of evolution of chronic hepatitis C, projected by the model, with the same parameter extracted from studies examining the long-term prognosis of chronic hepatitis C. The probability of developing cirrhosis, after 20 years of natural disease evolution estimated by our model, was of 17.3%, which is consistent with the same probability published in other studies [21,39 - 43].



This study examined the effectiveness and cost-effectiveness (utility) of treating chronic hepatitis C with PegIFN alpha 2b of 12 kD, compared to IFN alpha 2b (conventional) regimen in Brazilian patients, 30 years of age in average, using a Markov model to estimate the incremental cost-utility (ICU) in such patients, in the Brazilian 2006 private healthcare setting perspective.

The outcomes projected by this model were compared to the epidemiological data not used to build the model [21]. The epidemiological data usually used for this purpose was the probability to develop cirrhosis after 20 years of chronic hepatitis C natural evolution [21,39,42]. A 17.3% probability was estimated in a cohort of patients with mild chronic hepatitis C, a value being consistent and coherent with the published studies [21,39-43]. Therefore, the model probably represents with good accuracy the expected course of this disease, in the absence of antiviral treatment [21].

Additionally, the model projected the life expectation and quality adjusted life years for patients receiving no treatment, and achieved results being quite consistent with those from other already published models [21].

The therapeutic regime with PegIFN alpha 2b produced an average survival benefit of 0.51 discounted year of life, compared to IFN alpha 2b, in a life-time window. Although a gain of six incremental months of survival could appear tiny, it is consistent with the benefit resulting from other interventions to treat hepatitis C [21].

In genotype 1 patients, the cost-utility rate of PegIFN alpha 2b compared to IFN alpha 2b is higher because these patients should be treated for a longer time (48 weeks), have a SVR rate being lower than those for genotype 2 and 3 patients and, hence, they have a higher number of complications resulting from the disease evolution and, consequently, higher expenses and healthcare resources consumption.

The opposite occurs in genotype 2 and 3 patients. They are treated for a shorter period of time, 24 weeks, have higher SVR rate, with lower number of complications due to disease evolution and, therefore, lower consumption of healthcare resources.

However, genotype 1 patients generate larger benefit, in terms of life expectation and quality, in a life-time window, compared to IFN alpha 2b patients.

We could observe as well, that cirrhosis and its complications are the health statuses generating the main differences, in terms of financial resources consumption, between the regimes with PegIFN alpha 2B and conventional IFN alpha 2b.

The expenditure with drugs is 87.6% larger with the PegIFN alpha 2b therapy, but the cost incurred with the disease evolution treatment is 30% higher with the IFN alpha 2b therapy. Overall, the costs of PegIFN alpha 2b are 34.8% higher than those with IFN alpha 2b. However, with the cost-utility calculations, we could observe that, despite of being more expensive, the PegIFN alpha 2b treatment is cost-effective, seen under the WHO point of view related to the Brazilian healthcare market [15,16]. This result does not modify when we separately analyze both patients populations, genotype 1 and non-1 patients.

The global calculated cost-utility, R$19,848.34 per quality-adjusted life year gained is a single point estimation, is subjected to biases due to the uncertainties inherent to the model parameters. These uncertainties were considered by the sensitivity analyses and Monte Carlo simulations.

The incremental cost-utility rates are stable in the vast majority of circumstances, as duly shown by the Monte Carlo simulations.

The Monte Carlo simulation shows that the treatment with PegIFN alpha 2b, along an entire life time window, is cost-effective in 90.27% and 95.54% of the times, for patients with HCV genotypes 1 and non-1, respectively. This means that, if we consider the value of R$37,493.00, which according to the WHO suggestion is the threshold cost-utility ratio, PegIFN alpha 2b would have a probability of 90.27% for patients with genotype 1 HCV, and of 95.54% for patients with genotype non-1 HCV, to be accepted as a cost-effective treatment of chronic hepatitis C.

Except for a single work [21], "utilities" based on patients or on the community are not available, therefore, the patients' preferences have been estimated by experts [8,13,44]. Given the limited data coming directly from patients, we decided to use the already recognized data from literature [8,13].

We should emphasize that the "utilities" used in this model, despite being classic, are lower than those presented in other works [21].

Another topic to be commented is the possibility of our study underestimate the costs related to disease and, probably, underestimate the resource savings resulting from the treatment itself, due to the avoidance of future clinical complications. We used variable costs and have not considered fixed costs, not even those related to loss of productivity. The model also does not include the cost of other treatments for non-responsive patients and, the histological normalization and decrease of hepatocarcinoma incidence in non-responsive patients were not considered, as well.

Limitations of this Model

The clinical impact of the PegIFN alpha 2b regime was based only in a single clinical trial, by Manns et al., published at Lancet in 2001 [6].

Because we do not have "utilities" described for the different chronic hepatitis C health states for Brazilian patients, the quality adjusted life years may be subject of criticism.

The average clinical management was obtained from Delphi panels with Brazilian hepatologists, oncologists and intensivists; nevertheless, some variability in the cases management is possible, causing some cost differences. Then again, the sensitivity analysis studied this, and the model was not sensitive to these cost parameters.

Although there are many other possible health states that could be inserted in a chronic hepatitis C model, the simplification of the states and their transitions was necessary, in order to obtain a usable Markov model.

But, besides these limitations in the modeling technique, there are advantages that should be pointed out.

The ideal design to demonstrate the possible PegIFN alpha 2b regime long-term economic outcomes benefit compared to IFN alpha 2b regime, would be a naturalistic prospective study, which would require a long follow-up period under the economic perspective (from 15 to 35 years); and this is not feasible.

The use of decision techniques allows the extrapolation of clinical outcomes, beyond the duration of available clinical trials. Validation and sensitivity analyses were performed when feeling that the uncertainty would be big. In this model, the sensitivity analyses have been done with health states costs, utilities, and transition probabilities. These analyses demonstrate the results robustness in relation to the base-case parameters variation.



The results from this model suggest that the regimen with PegIFN alpha 2b is cost-effective compared to the IFN alpha 2b regimen, in patients with chronic hepatitis C. PegIFN alpha 2b is important in the global treatment cost of patients with chronic hepatitis C, however, this apparently voluminous initial investment decreases substantially the subsequent costs due to the chronic disease progression.



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Address for correspondence:
Dr. Marcelo Cunio Machado Fonseca
Avenida Higienópolis, 240 - apto 52C. Higienópolis
São Paulo - São Paulo - Brazil. Zip code: 01238-000

Received on 18 March 2009; revised 12 June 2009.

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