Baseline anti-NS4a antibodies in combination with on-treatment quantitative HCV-RNA reliably identifies nonresponders to pegylated interferon-ribavirin combination therapy after 4 weeks of treatment

Eur J Gastroenterol Hepatol. 2010 Dec;22(12):1443-8. doi: 10.1097/MEG.0b013e32833ef6e3.

Abstract

Background: Early detection of nonresponders to hepatitis C therapy limits unnecessary exposure to treatment and its side-effects. A recent algorithm combining baseline anti-NS4a antibodies and on-treatment quantitative PCR identified nonresponders to a combination of interferon and ribavirin after 1 week of treatment.

Aim: To validate a stopping rule based on baseline anti-NS4a antibody levels and early on-treatment virological response in treatment-naive genotype 1 chronic hepatitis C patients treated with the current standard pegylated interferon and ribavirin combination therapy.

Methods: Eighty-nine genotype 1 patients from the Dynamically Individualized Treatment of hepatitis C Infection and Correlates of Viral/Host dynamics Study treated for 48 weeks with standard 180 μg pegylated interferon (PEG-IFN)-α-2a (weekly) and ribavirin 1000-1200 mg (daily) were analysed. Baseline anti-NS4a antibody enzyme-linked immunosorbent assay (NS4a AA 1687-1718) was performed on pretreatment serum. Hepatitis C virus-RNA was assessed at days 0, 1, 4, 7, 8, 15, 22, 29, weeks 6, 7, 8, 10, 12 and 6 weekly thereafter until end of treatment. Multiple regression logistic analysis was performed.

Results: Overall 54 of 89 (61%) patients achieved sustained virological response. A baseline anti-NS4a antibody titre less than 1/1250 correlated with absence of favourable initial viral decline according to variable response types (P = 0.015). The optimal algorithm was developed using the combination of the absence of anti-NS4a Ab (<1/1250) at baseline and the presence of a viral load ≥ 100.000 IU/ml at week 4. This algorithm has a specificity of 43% and negative predictive value of 100% to detect nonresponse to standard PEG-IFN-α-2a and ribavirin therapy at fourth week of therapy (intention-to-treat analysis).

Conclusion: The decision to stop the therapy in genotype 1 chronic hepatitis C patients treated with PEG-IFN-α-2a and ribavirin can be confidently made after 4 weeks of treatment based on the absence of baseline anti-NS4a Ab and a week-4 hepatitis C virus-RNA above 100.000 IU/ml.

Publication types

  • Clinical Trial, Phase III
  • Multicenter Study

MeSH terms

  • Adult
  • Aged
  • Algorithms
  • Antiviral Agents / therapeutic use*
  • Biomarkers / blood
  • Carrier Proteins / immunology*
  • Decision Support Techniques
  • Drug Therapy, Combination
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Genotype
  • Hepacivirus / genetics*
  • Hepacivirus / immunology*
  • Hepatitis C / blood
  • Hepatitis C / diagnosis
  • Hepatitis C / drug therapy*
  • Hepatitis C Antibodies / blood*
  • Humans
  • Interferon alpha-2
  • Interferon-alpha / therapeutic use*
  • Intracellular Signaling Peptides and Proteins
  • Logistic Models
  • Male
  • Middle Aged
  • Patient Selection
  • Polyethylene Glycols / therapeutic use*
  • Predictive Value of Tests
  • RNA, Viral / blood*
  • Recombinant Proteins
  • Reproducibility of Results
  • Ribavirin / therapeutic use*
  • Sensitivity and Specificity
  • Time Factors
  • Treatment Failure
  • Viral Nonstructural Proteins / immunology*
  • Young Adult

Substances

  • Antiviral Agents
  • Biomarkers
  • Carrier Proteins
  • Hepatitis C Antibodies
  • Interferon alpha-2
  • Interferon-alpha
  • Intracellular Signaling Peptides and Proteins
  • NS4A cofactor peptide, Hepatitis C virus
  • RNA, Viral
  • Recombinant Proteins
  • Viral Nonstructural Proteins
  • Polyethylene Glycols
  • Ribavirin
  • peginterferon alfa-2a