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Fast relapse and high drop out rate of 48 weeks daily interferon monotherapy in HIV-infected patients with chronic hepatitis C
© Bruno et al; licensee BioMed Central Ltd. 2002
Received: 26 April 2002
Accepted: 28 August 2002
Published: 28 August 2002
The standard of care for HCV Hepatitis is the combination of interferon (IFN) plus Ribavirin. In HIV patients the use of this combination therapy may induce drug interactions, and reduces the adherence to HAART.
The aim of this study is to evaluate safety and efficacy of a 48 weeks daily dose IFN schedule.
We evaluated 50 coinfected patients; alpha IFN 2a was administered at a dose of 3 MU daily. The baseline values were the following : CD4+ 515 cells/mmc (mean); HIV-RNA <50 copies/ml in all patients; HCV-RNA 28, 3 × 106 copies/ml.
At 48 weeks, 10 patients (20%) achieved a biochemical and virological response according to an intention to treat analysis.
Twenty four patients (48%) underwent a drop-out mainly by side effects related to overlapping toxicity of interferon and antiretroviral therapy. All the patients, who responded to the treatment, showed a fast relapse one month after the end of treatment.
Although our results demonstrated a very poor outcome and a bad tolerance to interferon monotherapy, this approach should not be dropped out, mainly in patients at high risk for side effects and in those with cirrhosis who do not tolerate or are at increased risk for the use of ribavirin.
HIV – hepatitis C virus (HCV) coinfection is common and affects more than one third of all HIV infected persons worldwide. Prevalence among risk categories varies according to shared risk factors for transmission, mainly Intravenous Drug Use (IDU) and haemophiliacs . Chronic HCV infection seems to accelerate the course of HIV disease, resulting in a worsened clinical and immunological progression. At the same time, several studies suggest that HIV disease modifies the natural history of HCV infection, leading to a faster course of progression from active hepatitis to cirrhosis, to end stage liver disease and death [3–6]. HCV infection mimics opportunistic diseases because its natural history is significantly accelerated in HIV patients .
Since 1996 Higly Active Antiretroviral therapy (HAART) has slowed the progression of HIV disease and decreased the rate of HIV associated mortality.
Because the prognosis of HIV disease has been modified by HAART, the need to treat HCV coinfection became a significant issue. However, few studies have described the use of Interferon-α for treatment of chronic HCV infection in HIV infected patients. The reports of Boyer  and Marriot  showed a poor sustained response. In the largest up to now published study, Soriano  described that the 20% of patients achieved a sustained virological response; in this study Interferon-α appeared to be well tolerated. These results have been obtained with a thrice weekly (TIW) Interferon schedule. Strategies to improve the response to therapy are needed to modify the progression of HCV related liver diseases. Combination therapy with Interferon alpha 2b and ribavirin (RBV) is effective in immunocompetent patients, at least in 60% of those achieving an end of treatment virological response (ETR) and in 45% showing a sustained virological response (SVR) 6 months after stopping IFN and RBV(12, 13). In mono infected patients with severe chronic hepatitis the percentage of SVR is about 35% . The need for a more aggressive therapy in HIV-HCV patients is justified by the worsened clinical course. A significant problem in the treatment of coinfection arises from the complexity of both HAART and standard of care regimen for HCV hepatitis. Indeed, the use of combination therapy with IFN plus ribavirin may induce drug interactions, (in vitro studies have demonstrated that ribavirin could affect intracellular phosphorylation of deoxynucleoside, mainly AZT,  leading to a reduced therapeutic effect), increases the pill burden, reducing the adherence to HAART, and the risk of mithocondrial toxicity (16, 17). In our previous study performed in immunocompetent patients we demonstrated that daily IFN administration is more effective than TIW.
On this basis we have attempted to treat coinfected patients with a daily interferon schedule, in order to improve the percentage of clinical response.
The aim of this pilot study is to evaluate the efficacy and safety of an aggressive daily schedule of 3 MU α Interferon in the treatment of HCV related chronic hepatitis in patients infected with HIV.
Baseline demographic characteristics of the patients
Number of patients
Past history of alchol abuse (%)
Estimated duration of HCV infection(months) [mean ± SD]
29,2 ± 13,1
Antiretroviral Therapy (%)
Mean CD4 cells/mmc count (range)
<50 copie/ml in all patients
28,3 × 106 copies/ml
7 ± 3
Surrogate markers for hepatitis C and HIV disease
Serum levels of alanine amino transferase (ALT normal ≤ 39 IU/l), aspartate aminotransferase (AST; normal, ≤ 34 IU/l), gamma glutamyl transferase (GGT normal, ≤ 53 IU/l) and bilirubin (normal ≤ 1.10 mg/l) were measured using standard methods. Serum HCV RNA was measured by a qualitative PCR assay (COBAS Amplicor HCV, version 2.0, limit of detection of 100 copies/milliliter), and quantitative HCV RNA was evaluated by a branched DNA signal amplification assay test (Quantiplex HCV RNA 2.0, Chiron, Emeryville, California, USA; range of detection, 200.000 – 120.000.000 geq/ml). The HCV genotype was determined by hybridization of biotin-labelled PCR products to oligonucleotide probes bound to nitrocellulose membrane strips (Inno-Lipa; Innogenetics, Brussels, Belgium). Absolute numbers of CD4 cells in whole blood were determined by flow cytometry. Serum levels of HIV-RNA were determined by the branched DNA test (Quantiplex HIV RNA 2.0; Chiron; threshold: 50 copies/ml). Both HIV-RNA levels and CD4 cells count were measured at baseline and after four, eight, twelve weeks and, subsequently every three months. Hepatic inflammation and fibrosis were graded using the modified Knodell histological activity index. The inflammation score was determined by combining the first free index scores: portal, periportal and lobular inflammation. The inflammation score has a range from 0 to 18; the higher score indicates more severe histological abnormalities. The degrees of fibrosis were: 0, no fibrosis; 1, portal fibrosis; 3, bridging fibrosis and 4 cirrhosis.
The primary efficacy end point was a sustained virological response (SVR) defined as a lack of detectable HCV-RNA in the serum at 24 weeks after the treatment was completed. A secondary end point was the presence of a end of treatment response (ETR), defined as the absence of serum HCV-RNA at the end of 48 weeks of therapy. Adverse events, both clinical and laboratory, were checked at every scheduled visit.
Analysis of results was carried out using an as treated (where only patients carrying on treatment were included) and an intent to treat analysis, where missed data were considered as failure. Quantitative variables to compare baseline and follow-up values from individual patients were compared by using the t test for paired samples, after log transformation, where appropriate. Results are expressed as mean ± SD.
We did not observe a reduction neither in absolute count nor in percent of CD4 cells. Only transient blips of HIV viremia were recorded with values less than 1000 copies/ml.
The mean ALT value in the study population were 169 ± 129 at baseline. The necrotic-inflammatory and fibrosis scores. were 7 ± 3 and 2 ± 1, respectively. Seven out of the 50 patients showed histological evidence of cirrhosis (14%). At baseline HCV viremia was 28.3 ± 36.6 × 106 genome equivalents (geq)/ml. Only twenty six individuals completed 48 weeks of treatment without any serious or potentially life-threatening adverse events; there were no drug-related deaths. The mean duration of therapy was 23 ± 19 weeks.
After 24 weeks of therapy, the mean levels of ALT decreased to 131 ± 61 UI/l (p = NS). At this time HCV viremia was 9.2 ± 12.4 × 106 genome equivalents (geq)/ml (p = 0.66). The as treated analysis showed a percentage of responders of 58% (29/50). The intention to treat analysis showed a percentage of responders of 44% (22/50).
After 48 weeks of therapy, the mean levels of ALT decreased to 95 ± 61 UI/l (p = NS). At this time HCV viremia was 1.4 ± 1.6 × 106 genome equivalents (geq)/ml (p = 0.07). The percentage of responders decreased to 38% (19/50) according to an as treated analysis, and to 20% (10/50) according to an intention to treat analysis. Among end of treatment virological responders 6 patients were genotype 3A, while 4 were genotype 1. One of them was cirrhotic.
Laboratory findings at 24 weeks, end of treatment and one month after end of treatment.
End of treatment (ETR) 12 months
1 month after end of treatment
ALT UI/ml (mean ± SD)
169 ± 129
131 ± 61
95 ± 61
79 ± 75
HCV-RNA × 106geq/ml (mean ± SD)
28.3 ± 36.6
9.2 ± 12.4
1.4 ± 1.6
39.07 ± 20.22
Among patients who completed treatment, 4 had interferon dose reduction due to leukopenia; 2 out of the responder ones.
Side effects leading to interruption
Number of patients (total n = 24)
Lost to follow up
HIV coinfection has been considered until a couple of years ago as an exclusion criteria in all the controlled trials on efficacy of interferon used as monotherapy and in combination with ribavirin. So, available data comes out from pilot studies or comparative studies versus HIV uninfected patients. Three hundred and eighty eight patients have been enrolled in the 12 studies published as full papers on interferon monotherapy. None of these studies was placebo controlled; both interferon alfa 2a and 2b were used with doses ranging from 1 million units three times per week to 9 MIU daily. Arbitrarily cumulating these data, end of treatment response was obtained in 28% of treated patients and sustained response in 16%. Ten per cent of patients dropped out. In the largest published study, Soriano et al described how 20% of patients achieved a sustained virological response . Summarizing the five studies, comparing sustained response rate in HIV seropositives and seronegatives we can identify a slightly lower rate of sustained response in HIV seropositives in all the trials; however this difference did not reach statistical significance in any of them .
Analyzing all these studies, ranked according to the year of publication, we can identify a sharp decrease in the rate of sustained response in the studies published in the last 3 years [21–23]. The change in response rate to interferon monotherapy could probably be related to a change of the kind of patients which have been included in the HAART era. Recently have become to be treated the most difficult patients with advanced fibrosis, unfavourable genotypes, high HCV viremia and lower CD4 counts.
Actually the standard of care for chronic hepatitis C in immunocompetent patients has become the combination therapy of interferon and ribavirin, but so far there are only few published data obtained in HIV-HCV coinfected patients with an impressive difference of sustained response rate among the studies .
However, the use of combination therapy with IFN plus ribavirin may induce drug interactions, (in vitro studies have demonstrated that ribavirin could affect intracellular phosphorylation of deoxynucleoside, mainly AZT, and d4t, leading to a reduced therapeutic effect), increases the pill burden, compromising the adherence to HAART, and the risk of mithocondrial toxicity.
The finding that NRTIs may interfere with mitochondrial DNA synthesis led to many studies evaluating these effects in vitro. These studies suggested a ranking of ddC>ddI>d4T>3TC>AZT>ABC for effects on mitochondrial polymerase gamma [26, 27].
Because each NRTI has a different affinity for mitochondrial polymerase gamma, they could have a different capacity for inducing liver toxicity.
Hence, the choice of treatment of both hepatitis C and HIV must be oriented toward drugs with lower overlapping toxicity, mainly if ribavirin is used. This approach could be useful to increase the safety of therapy of coinfection and to avoid cases of fatal lactic acidosis. The use of interferon alone may reduce the incidence of such therapy related adverse events. In this setting we tried to use an aggressive daily interferon schedule (3 MU daily) which in immunocompetent patients gave us a good sustained response rate .
In the present study we report an ETR rate of 20% and a SVR rate of 0%, with all patients relapsing one month after stopping the therapy. The ETR rate is comparable to that observed either in immunocompetent patients or in HIV-HCV coinfected patients treated with interferon alone three times weekly. This percentage of ETR observed in our study has been reduced by the high incidence of side effects due to the overlapping toxicity of both antiretroviral and interferon therapy. The SVR was 0% and may probably be influenced, as observed in other studies with low SVR rate [21–23], by the lack of immune-clearance which regulates the late phase of viral decay. Indeed the more rapid is the viral decay, the higher is the probability of SVR .
Although a CD4 cell count threshold of less than 200 cells/mmc has been reported to reduce the likelihood of SVR, this has not been observed in our patients who did not respond, in spite of having more than 200 CD4 cells/ mmc. Most of the adverse events encountered in this study were similar to those reported in HIV seronegative immunocompetent patients, but they were emphasized by the concomitant administration of antiretrovirals which made the patients intolerant to both treatment, resulting in a very high drop out rate.
So far the optimal treatment schedule for HCV has not yet been established in co-infected patients. Several studies are ongoing to determine if the outcome could be improved by the use of pegylated interferon plus ribavirin, with promising preliminary results. Data on pegylated interferon alone in HIV patients are actually lacking. Although our results have demonstrated a very poor outcome with interferon monotherapy, this approach should not be completely dropped out, especially using PEG Interferon, mainly in patients at high risk for side effects and in those with cirrhosis who do not tolerate or are at increased risk for the use of ribavirin. This strategy could be useful to increase the safety of therapy of coinfection and to avoid cases of severe liver toxicity and lactic acidosis.
However, depending upon the baseline CD4 cell count level, in patients with more than 350 CD4+/mmc, hepatitis treatment should precede antiretroviral therapy to reduce the overall risk of toxicity.
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