4.8 Article

Prolonged Therapy of Advanced Chronic Hepatitis C with Low-Dose Peginterferon

Journal

NEW ENGLAND JOURNAL OF MEDICINE
Volume 359, Issue 23, Pages 2429-2441

Publisher

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa0707615

Keywords

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Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases
  2. National Institute of Allergy and Infectious Diseases
  3. National Cancer Institute,
  4. National Center for Minority Health and Health Disparities
  5. National Center for Research Resources
  6. National Institute on Alcohol Abuse and Alcoholism [K24 AA13736]
  7. Hoffmann-La Roche
  8. Idenix Pharmaceuticals
  9. Novartis
  10. Vertex Pharmaceuticals
  11. Bristol- Myers Squibb
  12. Abbott
  13. Schering-Plough
  14. Anadys
  15. GlobeImmune
  16. Pharmasset
  17. SciClone Pharmaceuticals
  18. Clinical Care Options
  19. Gilead
  20. Geneva Foundation
  21. Hoffmann La Roche
  22. Biolex
  23. Valeant Pharmaceuticals
  24. GlaxoSmithKline
  25. Novartis/Human Genome Sciences
  26. King Pharmaceuticals
  27. Peregrine Pharmaceuticals
  28. Roche Diagnostics
  29. ZymoGenetics
  30. Wyeth Pharmaceuticals
  31. Eli Lilly
  32. FibroGen
  33. AstraZeneca
  34. Siemens
  35. Ovation Pharmaceuticals
  36. Boehringer-Ingelheim
  37. Cardax Pharmaceuticals
  38. Achillion Pharmaceuticals
  39. Avant Immunotherapeutics
  40. CombinatoRx
  41. Cubist Pharmaceuticals
  42. Nucleonics
  43. Oxxon
  44. Metabasis
  45. Amgen
  46. Biogen
  47. EnablEd and Clinical Care Options

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Background: In patients with chronic hepatitis C who do not have a response to antiviral treatment, the disease may progress to cirrhosis, liver failure, hepatocellular carcinoma, and death. Whether long-term antiviral therapy can prevent progressive liver disease in such patients remains uncertain. Methods: We conducted a randomized, controlled trial of peginterferon alfa-2a at a dosage of 90 microg per week for 3.5 years, as compared with no treatment, in 1050 patients with chronic hepatitis C and advanced fibrosis who had not had a response to previous therapy with peginterferon and ribavirin. The patients, who were stratified according to stage of fibrosis (622 with noncirrhotic fibrosis and 428 with cirrhosis), were seen at 3-month intervals and underwent liver biopsy at 1.5 and 3.5 years after randomization. The primary end point was progression of liver disease, as indicated by death, hepatocellular carcinoma, hepatic decompensation, or, for those with bridging fibrosis at baseline, an increase in the Ishak fibrosis score of 2 or more points. Results: We randomly assigned the patients to receive peginterferon (517 patients) or no therapy (533 patients) for 3.5 years. The level of serum aminotransferases, the level of serum hepatitis C virus RNA, and histologic necroinflammatory scores all decreased significantly (P<0.001) with treatment, but there was no significant difference between the groups in the rate of any primary outcome (34.1% in the treatment group and 33.8% in the control group; hazard ratio, 1.01; 95% confidence interval, 0.81 to 1.27; P=0.90). The percentage of patients with at least one serious adverse event was 38.6% in the treatment group and 31.8% in the control group (P=0.07). Conclusions: Long-term therapy with peginterferon did not reduce the rate of disease progression in patients with chronic hepatitis C and advanced fibrosis, with or without cirrhosis, who had not had a response to initial treatment with peginterferon and ribavirin. (ClinicalTrials.gov number, NCT00006164.).

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