Combination and Intermittent Therapy Based on Pegylated Interferon Alfa-2a for Chronic Hepatitis B with Nucleoside (Nucleotide) Analog-Experienced Resulting in Hepatitis B Surface Antigen Clearance: A Case Report

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Meisam Mahdavi ◽  
Houshang Amirrasouli ◽  
Seyed Moayed Alavian ◽  
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The Lancet ◽  
2005 ◽  
Vol 365 (9454) ◽  
pp. 123-129 ◽  
Author(s):  
Harry LA Janssen ◽  
Monika van Zonneveld ◽  
Hakan Senturk ◽  
Stefan Zeuzem ◽  
Ulus S Akarca ◽  
...  

2011 ◽  
Vol 10 (1) ◽  
pp. 84-87 ◽  
Author(s):  
Mangano Carmelo ◽  
Squadrito Giovanni ◽  
Cacciola Irene ◽  
Carpentieri Mariastella ◽  
Foti Giuseppe ◽  
...  

2011 ◽  
Vol 152 (22) ◽  
pp. 869-874 ◽  
Author(s):  
István Tornai

Treatment of chronic hepatitis B is still challenging. Lots of parameters are needed to be considered before and during the therapy. There are several possible endpoints and their durability is very much variable. Patients with HBeAg-positive and HBeAg-negative hepatitis B need treatment. Two different strategies are available. Interferon-based therapy is a limited treatment, which might result in a sustained immune response in about one third of the patients, leading to an induced remission, sometimes years after the end of the treatment. According to the other strategy a continuous, indefinite oral nucleoside/nucleotide analogue (NA) treatment is administered to maintain a remission. However, relapse is rather frequent after the cessation of this therapy. During the long-term NA treatment drug resistance can lead to the loss of antiviral effect. Three first-line drugs are recommended, pegylated interferon alfa-2a, entecavir and tenofovir. If there is no contraindication to interferon, it is worth trying to achieve immune control and an induced remission. In patients, who do not respond to interferon, a sequential NA therapy is indicated. Orv. Hetil., 2011, 152, 869–874.


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