Short duration treatment in genotype 1 chronic hepatitis C patients with rapid virologic response to pegylated interferon plus ribavirin
Autor: | Rinaldo Pellicano, Aldo Manca, Alessia Ciancio, Marco Tabone, R. Bonardi, Mario Rizzetto |
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Rok vydání: | 2011 |
Předmět: |
Male
Time Factors Cost-Benefit Analysis Hepacivirus Gastroenterology Polyethylene Glycols chemistry.chemical_compound Liver Function Tests Recurrence Pegylated interferon Chronic Hepatitis C therapy genotype 1 short treatment medicine.diagnostic_test virus diseases General Medicine Hepatitis C Middle Aged Viral Load Recombinant Proteins Treatment Outcome Predictive value of tests Drug Therapy Combination Female Viral load medicine.drug Adult medicine.medical_specialty Genotype Antiviral Agents Drug Administration Schedule Pharmacotherapy Predictive Value of Tests Internal medicine Ribavirin medicine Humans Rapid Virologic Response Pharmacology Dose-Response Relationship Drug business.industry Interferon-alpha Hepatitis C Antibodies Hepatitis C Chronic medicine.disease digestive system diseases chemistry Immunology Liver function tests business |
Zdroj: | Biomedicine & Pharmacotherapy. 65:303-306 |
ISSN: | 0753-3322 |
DOI: | 10.1016/j.biopha.2011.03.004 |
Popis: | Background In patients with chronic hepatitis C, rapid HCV-RNA clearance under treatment might allow shorter treatment duration without modifying the sustained virological response (SVR) rate. This study evaluated the impact of rapid virological response (RVR) in HCV genotype 1b infection management. Methods In an open-label trial, 180 patients received standard doses of peginterferon alfa-2a plus ribavirin. Those with undetectable serum HCV-RNA at week 6 (RVR) received 24-week short-course treatment; patients with undetectable HCV-RNA at week 12 (early responders [ER]) received 48-week “standard of care” treatment; patients with positive HCV-RNA at week 12 (non-responders [NR]) stopped the treatment. Study end-point was to determine SVR rate at week 24. Results The following responses were observed: 24% RVR, 44% ER, 32% NR. Among RVR subjects, HCV-RNA baseline levels and age were significantly lower (P = 0.038 and 0.035 respectively) than in non-RVR patients. At follow-up, 91% of RVR and 33% of ER patients achieved SVR. Among those with RVR, patients experiencing post-therapy relapse were older than those who achieved a SVR (P = 0.028). Conclusions Chronic HCV-1b patients, achieving RVR with a 24-week treatment regimen, attained excellent SVR rates. In a cost-effective therapeutic approach, all HCV-1b patients eligible for therapy may have a short duration therapy on the basis of RVR. |
Databáze: | OpenAIRE |
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