Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2003-6-13
pubmed:abstractText
Patients with chronic hepatitis C infected with HCV genotype 2 and 3 can be successfully treated in more than 80 % of cases. It had been shown that a 24 week t.i.w. treatment period with standard interferon alpha and ribavirin is sufficient for these patients. However, the recent multicenter studies investigating the effect of pegylated interferons and ribavirin used a 48 week schedule for all patients irrespective of the HCV genotype. Thus, we prospectively investigated the efficacy of a 24 week treatment period with pegylated interferon alpha-2b (1.0-1.5 microg/kg o.i.w.) and ribavirin (1-1.2 g daily) in 54 patients with HCV-genotype 2 and 3 at two different sites. 29 patients were included in Herne (private practice) and 25 patients were treated in Hannover (Medical School). After the end of follow-up 46 (85%) patients showed a virological sustained response in the intent to treat analysis. Only four patients demonstrated a virological treatment failure (3 relapse, 1 breakthrough), two patients were non-compliant, and at each center therapy was stopped in one patient due to adverse events. There was no difference regarding treatment response between both sites, even though the patients in Herne were treated only with 1,0 microg/kg PEG-IFN alpha-2b, while patients in Hannover received 1,5 microg/kg PEG-IFN alpha-2b. In conclusion, the response rates of this study do not differ from the results of the 48 week treatment period of the recently published multicentre trials. Thus, we suggest treating all patients with HCV-genotype 2 and 3 for only 24 weeks when PEG-IFN alpha-2b is used in combination with ribavirin.
pubmed:language
ger
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0044-2771
pubmed:author
pubmed:issnType
Print
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
517-22
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:12806536-Adolescent, pubmed-meshheading:12806536-Adult, pubmed-meshheading:12806536-Aged, pubmed-meshheading:12806536-Antiviral Agents, pubmed-meshheading:12806536-Drug Therapy, Combination, pubmed-meshheading:12806536-Female, pubmed-meshheading:12806536-Follow-Up Studies, pubmed-meshheading:12806536-Genotype, pubmed-meshheading:12806536-Hepacivirus, pubmed-meshheading:12806536-Hepatitis C, Chronic, pubmed-meshheading:12806536-Humans, pubmed-meshheading:12806536-Interferon-alpha, pubmed-meshheading:12806536-Male, pubmed-meshheading:12806536-Middle Aged, pubmed-meshheading:12806536-Multicenter Studies as Topic, pubmed-meshheading:12806536-Prospective Studies, pubmed-meshheading:12806536-RNA, Viral, pubmed-meshheading:12806536-Recombinant Proteins, pubmed-meshheading:12806536-Ribavirin, pubmed-meshheading:12806536-Time Factors
pubmed:year
2003
pubmed:articleTitle
[Treatment of chronic hepatitis C with PEG-interferon alpha-2b and ribavirin: 24 weeks of therapy are sufficient for HCV genotype 2 and 3].
pubmed:affiliation
Abteilung für Gastroenterologie, Hepatologie und Endokrinologie, Medizinische Hochschule Hannover.
pubmed:publicationType
Journal Article, Comparative Study, English Abstract, Research Support, Non-U.S. Gov't