Introduction
In the 1990s, chronic hepatitis C virus (HCV) infection began to be treated with an interferon alpha (IFN-α) monotherapy. Dependent on HCV genotype, viral load, IFN-α dose, and treatment duration, sustained virological response (SVR) rates of up to 55% could be achieved in patients with HCV non-1 genotypes [
1]. Patients with HCV genotype 3 (HCV-G3) infection had SVR rates of 38% [
2] to 67% [
3] dependent of IFN-α dose. Studies that compared conventional IFN-α monotherapy to PEGylated interferon alpha (PEG-IFN-α) monotherapy achieved SVR rates of 28–46 and 38–68%, respectively [
4,
5]. Furthermore, studies that compared the efficacy of the combination therapy of PEG-IFN-α or IFN-α and ribavirin (RBV) to monotherapy used IFN-α dose of 3 million units three times per week. SVR rates of patients with HCV-G3 were thus 21–32% [
6,
7] for IFN-α and 38–45% for PEG-IFN-α [
5,
8]. In subpopulations of HCV-G3 patients with low baseline viral load, 58% of those who were treated with PEG-IFN-α achieved SVR [
8]. However, currently the standard treatment for patients with HCV-G3 is a combination therapy of PEG-IFN-α/RBV for 24 weeks attaining SVR rates of up to 80% [
9]. Current recommendations for treatment of HCV genotype 2 or 3-infected patients are based on the result of a trial that compared 24–48 weeks of treatment with PEG-IFN-α/RBV [
10]. Patients with HCV-G3 were treated with a schedule (RBV: 800 mg/day or 1,000/1,200 mg/day) similar to that of HCV genotype 1. A subsequent study of chronic HCV genotype 2 or 3-infected patients with PEG-IFN-α and 800 mg/day RBV but reduced duration [
11] showed that SVR rates in a subpopulation of patients with low virus load and rapid virological response (RVR) were similar. Dalgard et al. [
12] treated patients with chronic HCV-infected genotype 2 or 3 for 14 weeks with PEG-IFN-α and RBV 800 to 1,400 mg/day. SVR rates after 14 weeks of treatment were achieved more frequently among subtype 3a patients with low viral load and absence of bridging fibrosis/cirrhosis. A further study compared reduced doses of RBV (400 and 800 mg/day) for 24 weeks with equivalent outcomes in patients infected with HCV-G3 [
13].
Interestingly, comparison of combination therapy with IFN-α monotherapy in patients with early virological response in HCV genotype 2 or 3 showed no significant differences with regard to the outcome [
14]. Furthermore, two published studies showed acceptable SVR rates for patients with HCV genotype 2 or 3 after treatment with IFN-α monotherapy [
15,
16]. Patients with virological response between 7 days and 2 weeks have the greatest chance of achieving an SVR.
Since the combination therapy with RBV increases the rate of side-effects, the discontinuation rate is more frequent [
17]. The combination therapy is associated with a range of treatment-limiting serious adverse events in 4–9% in patients with HCV genotype 2 or 3 [
11]. Patients’ hemoglobin concentration decreases under combination therapy with RBV significantly [
18]. RBV-related anemia is an increased risk in patients with impaired renal dysfunction [
19]. Because of the teratogenicity and the accumulation of RBV, contraception is strictly essential during and 6 months after therapy.
For these reasons, the current strategy for the treatment of chronic HCV infection is to individualize the treatment duration guided to HCV genotype and on-treatment viral response. Since the efficacy of therapy significantly depends on the virus genotype and on the host’s clinical, biochemical, and genetic background [
20,
21], new therapeutic regimens have to be considered. Host genetic predictors for a successful therapy have been identified upstream of the interleukin 28B (IL28B)/IFN-λ3 gene. One single-nucleotide polymorphism (SNP), IL28B rs12979860, was independently and highly associated with SVR in patients with HCV genotype 1 [
22]. In HCV genotype 2b patients who were treated with combination therapy, IL28B SNP rs8099917 was an independent factor for SVR, and, conversely, patients with HCV genotype 2a treated with IFN-α monotherapy, IL28B SNP rs8099917 was also an independent factor for SVR [
23]. In patients with HCV-G3 treated with the combination therapy both IL28B-SNPs (rs12979860 and rs8099917) were not associated with SVR but with early virological response [
24]. The impact of these two SNPs regarding combination therapy or IFN-α monotherapy has not been reported. Two subgroups of patients with HCV-G3 at our center who were treated either with combination therapy or IFN-α
2a monotherapy provided the opportunity to assess the impact of the SNP rs12979860 and rs8099917 for SVR in addition to other clinical prognostic markers.
Discussion
In this retrospective uncontrolled and monocentric study, the experience of 66 consecutive patients infected with genotype 3 HCV who received either IFN-α2a monotherapy (n = 19) or combination therapy consisting of PEG-IFN-α and RBV (n = 36) or both (n = 11), is reported. The patients were treated for either 24 or 48 weeks. Six months after the EOT, 54/67 patients (82%) had achieved a SVR; 15/30 (50%) responded to IFN-α2a monotherapy while 32/36 (89%) responded to combination therapy with an additional 11 of having initially received monotherapy achieved a SVR with combination therapy. Factors associated with an SVR whether assessed pre- or on-treatment with IFN-α2a monotherapy were age (<40), the development of “ultra-rapid” virological response occurring within 2 weeks of the initiation of therapy and a low initial γ-GT/ALT-ratio. Factors associated with an SVR with the combination therapy were an RVR, decreases of Hb, WBC count, platelet count, and the degree of steatosis. The nadir Hb value on combination therapy was significantly lower than that of IFN-α2a monotherapy group.
In chronically HCV-infected patients, SVR rates range up to 80% among patients infected with genotype 2 or 3 [
9]. The therapeutic options for individuals with a genotype 3 infection are expanding. Recently, several studies have proposed new strategies for treatment of these patients. These include shortened duration of therapy [
28,
29], a reduced dose of RBV and duration of therapy [
30], and IFN-α
2a monotherapy [
16,
31]. These options for individuals infected with genotype 3 are of great interest because combination therapy has many side-effects, are teratogenic, and costly. Moreover, many individuals with a chronic HCV infection are of childbearing age and some have renal disease that makes the use of RBV difficult, if not impossible. As a result, individualized treatment options need to be considered and should be based upon recognized predictive factors for a SVR.
In recent years, many different factors predictive for a successful therapeutic outcome have been described. In addition to the HCV genotype [
10], host-specific clinical, laboratory, and genetic factors [
22,
26,
32‐
34] have been recognized. Pre-treatment laboratory factors such as γ-GT/ALT-ratio [
26,
34], AST to platelet ratio index (APRI) [
24,
35], or clinical and histological factors [
36] should also be considered in making a therapeutic decision.
In 2009, three different genome-wide association studies showed that various polymorphisms in the region of IL28B on chromosome 19 are highly associated with response in chronic HCV-genotype-1-infected patients after having sustained treatment with PEG-IFN-α and RBV therapy [
22,
37,
38]. These polymorphisms of IL28B were associated with response in treatment-naive and non-responders of genotype-1-infected patients. Yu et al. [
39] and Sakamoto et al. [
40] investigated the role of IL28B in chronic HCV-genotype-2-infected patients after treatment with PEG-IFN-α and RBV. While Yu et al. [
39] reported that the IL28B polymorphism did not predict a SVR but a RVR in HCV genotype 2 patients, Sakamoto et al. [
40] reported that patients infected with genotype 2b with the major allele of IL28B showed increased SVR rates. Recently, Moghaddam et al. [
24] examined the predictive ability of the IL28B polymorphism (rs12979860 and rs8099917) in patients with chronic HCV-G3 after treatment with combination therapy. They reported that these two SNPs are not predictive for a SVR. These results could be confirmed by Scherzer et al. [
41] who suggested an association between IL28B polymorphisms and the early virological response to the application of a PEG-IFN-α and RBV therapy, but no effect was observed on SVR rates in HCV-G3 patients. In this study, we examined the predictive ability of the mentioned IL28B polymorphisms above with regard to monotherapy, but since the sample size of both groups are small, the statistical analysis of IL28B genetic distribution does not have enough power to reveal a significant outcome. However, rather, the findings of either a ultra rapid or RVR [
24,
41] or a reduction in Hb [
18] during therapy are associated with a SVR.
One of the reasons for the low response to standard IFN-α is its short half-life, which leads to wide fluctuations in the plasma concentration of the drug during the treatment period. Because HCV has a high rate of turnover [
42], an intermittent increase in viral load can be observed in patients treated with standard IFN-α on treatment-free days [
43]. Despite these disadvantages, Bjoro et al. [
44] reported that in patients with genotype 2b/3a, low viral load and without cirrhosis the SVR rate could be increased by IFN-α induction (6 MU IFN-α
2a daily for 4 weeks) up to 61%. Akuta et al. [
45] and Yokosuka et al. [
46] reported SVR rates of 68 and 84% in selected groups of chronic HCV-genotype-2 treated with induction IFN-α monotherapy. In these two studies, 6-10 MU IFN-α was administered daily for 2–4 weeks. The addition of a polyethylene glycol molecule to interferon produces a biologically active molecule with a longer half-life. This characteristic allows a more convenient dosing, i.e., once a week. In case of only applying PEG-IFN-α to patients with chronic HCV (all genotypes) for 48 weeks, the SVR rate was approximately twice (39%) as high as the rate of having applied standard IFN-α to the patients [
5]. The subgroup analysis of the prospective randomized study by Fried et al. [
8] showed that all HCV-G3 patients achieved SVR rates of 45% after PEG-IFN-α monotherapy. Another prospective randomized study by Angelico et al. [
14] showed that selected groups of patients with HCV-genotype 2/3 had a SVR rate of 67% through the application of PEG-IFN-α therapy. Based upon these data, in patients infected with HCV-G3 who are young (<40 years), have a low viral load, histologically mild disease, and a low initial γ-GT/ALT-ratio, monotherapy with IFN-α is effective in 50% of the individuals treated. As mentioned above, considerable data on the use of PEG-IFN-α for the treatment of HCV-infected patients are available in the literature [
8,
9]. In contrast, daily dosing of IFN-α consisting of 3 MU for 24 weeks has been reported to achieve a 66.7% SVR rate. The patients who achieved an SVR had an initial virological response after only 2 weeks of IFN-α
2a monotherapy [
16]. These data are in accordance with the present results and suggest that the adverse effects of RBV can be avoided in a subgroup of patients with HCV-G3 who show an “ultra-rapid” virological response within 2 weeks of the start of IFN-α treatment. Those who do not achieve an “ultra-rapid” virological response can have RBV added to their therapy to enhance the likelihood of their achieving an SVR. This approach would eliminate the potential teratogenic effects of RBV in patients, reduce the severity of the anemia occurring during therapy, and reduce the cost of therapy in those receiving monotherapy who achieve an “ultra-rapid” virological response.
It needs to be recognized that important limitations to the present report exist: (1) It is a retrospective study, which was placed on (2) a single center, (3), which included only a small sample size referring to each group, and (4) with different therapy regimes within the groups. This study contains an explorative analysis for further suggestions of different therapy regimes for chronic HCV-G3 patients. In order to examine the hypothesis of this retrospective study, a prospective trail should be initiated that should include the suggested criteria by starting PEG-IFN-α2a monotherapy in selected patients.
In conclusion, patients, who are under 40 years, having a low viral load and a low initial γ-GT/ALT-ratio, absence of fibrosis/cirrhosis and steatosis, and who develop an on-treatment “ultra-rapid” virological response can achieve an SVR of 50%. This subgroup of patients may benefit from a treatment regimen consisting of PEG-IFN-α monotherapy.