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Ability of treatment week 12 viral response to predict long-term outcome in genotype 1 hepatitis C virus/HIV coinfected patients.

AbstractOBJECTIVE:
Guidelines recommendation to extend treatment duration in genotype 1 hepatitis C virus (HCV)/HIV-coinfected patients who clear the virus later than treatment week 4 is not evidence-based. Our main objective was to study the ability of week 12 viral response [early virologic response (EVR)] to predict long-term outcome in patients treated for 48 weeks.
DESIGN:
Multicenter retrospective cohort analysis.
METHODS:
Genotype 1 HCV treatment-naive, HIV-coinfected adult patients with compensated liver disease who started combination therapy with fixed-dose pegylated-interferon (pegIFN) alfa-2a or weight-based pegIFN alfa-2b plus ribavirin were included. Univariate and forward stepwise logistic regression analysis were used to identify predictors of sustained viral response (SVR) and relapse.
RESULTS:
By intention-to-treat analysis, 31.3% (87/278) of patients achieved an SVR. SVR rate was more than three-fold higher in patients who cleared the virus by week 12 of treatment compared with late responders. Among 123 end-of-treatment responders, 36 (29.3%) relapsed. Relapse risk increased in patients with cirrhosis, in those with ribavirin dose reductions and in late responders: more than 65% of patients who cleared the virus between weeks 12 and 24 relapsed following 48 weeks of treatment compared with 10% of those attaining a complete EVR (<15 IU/ml) at treatment week 12 (risk ratio 6.4, 95% confidence interval 2.9-14.4).
CONCLUSION:
Viral response at treatment week 12 is a strong predictor of long-term outcome. Genotype 1 HCV/HIV-coinfected patients who achieve a complete EVR (<15 IU/ml) are at low risk of viral relapse after completing the standard 48 weeks of therapy.
AuthorsEva Van den Eynde, Juan Manuel Tiraboschi, Cristina Tural, Ricard Solà, José Antonio Mira, Daniel Podzamczer, Antoni Jou, Nuria Cañete, Juan Antonio Pineda, Albert Pahissa, Manuel Crespo
JournalAIDS (London, England) (AIDS) Vol. 24 Issue 7 Pg. 975-82 (Apr 24 2010) ISSN: 1473-5571 [Electronic] England
PMID20299963 (Publication Type: Journal Article, Multicenter Study)
Chemical References
  • Antiviral Agents
  • Interferon alpha-2
  • Interferon-alpha
  • RNA, Viral
  • Recombinant Proteins
  • Polyethylene Glycols
  • Ribavirin
  • peginterferon alfa-2a
Topics
  • Adult
  • Antiviral Agents (administration & dosage)
  • Drug Administration Schedule
  • Female
  • Genotype
  • HIV Infections (drug therapy, genetics, virology)
  • HIV-1
  • Hepacivirus (genetics)
  • Hepatitis C, Chronic (drug therapy, virology)
  • Humans
  • Interferon alpha-2
  • Interferon-alpha (administration & dosage)
  • Male
  • Polyethylene Glycols (administration & dosage)
  • RNA, Viral (genetics)
  • Recombinant Proteins
  • Recurrence
  • Regression Analysis
  • Retrospective Studies
  • Ribavirin (administration & dosage)
  • Treatment Outcome
  • Viral Load

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