Skip to main content

Advertisement

Log in

Baseline risk factors for relapse in HIV/HCV co-infected patients treated with PEG-IFN/RBV

  • Clinical and Epidemiological Study
  • Published:
Infection Aims and scope Submit manuscript

Abstract

Purpose

Hepatitis C virus (HCV) viral relapse (VR) after end-of-treatment response (ETR) in human immunodeficiency virus (HIV) co-infected patients is observed in as many as one in three co-infected patients. The aim of the study was to identify baseline risk factors for VR in HIV/HCV co-infected patients treated with pegylated interferon plus ribavirin (PEG-INF/RBV).

Methods

A total of 212 Caucasian HIV-infected patients with chronic hepatitis C naïve for PEG-INF/RBV were followed prospectively. Patients were included in this prospective study if they had completed a full course of therapy with an ETR. We assessed the relationship between VR rate and potential predictors of relapse.

Results

Of the patients followed, 130 (61.3 %) attained ETR and 103 (79.2 %) achieved sustained virological response (SVR). Consequently, 27 (20.8 %) showed VR. Patients who relapsed were more often male (p = 0.036), carried the non-CC rs14158 genotype in the low-density lipoprotein receptor (LDLr) gene (p = 0.039), had higher baseline HCV RNA levels (p = 0.012), body mass index (BMI) ≥25 kg/m2 (p = 0.034), significant liver fibrosis (p < 0.001), had been diagnosed with acquired immunodeficiency syndrome (AIDS)-defining criteria in the past (p = 0.001) and bore the HCV genotypes 1/4 (p = 0.046) when compared with SVR patients. The IL28B genotype was not associated with relapse. Multivariate binary logistic regression showed that high baseline HCV RNA, significant liver fibrosis, HCV genotypes 1/4, being overweight and being diagnosed with AIDS-defining criteria in the past were independently associated with relapse.

Conclusions

Our study shows that VR can be accurately predicted in HIV/HCV co-infected patients on the basis of risk factors which can be identified before treatment.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Lauer GM, Walker BD. Hepatitis C virus infection. N Engl J Med. 2011;345:41–52.

    Article  Google Scholar 

  2. Operskalski EA, Kovacs A. HIV/HCV co-infection: pathogenesis, clinical complications, treatment, and new therapeutic technologies. Curr HIV/AIDS Rep. 2011;8:12–22.

    Article  PubMed  Google Scholar 

  3. Soriano V, Vispo E, Labarga P, Medrano J, Barreiro P. Viral hepatitis and HIV co-infection. Antivir Res. 2010;85:303–15.

    Article  PubMed  CAS  Google Scholar 

  4. Hadigan C, Kottilil S. Hepatitis C virus infection and coinfection with human immunodeficiency virus: challenges and advancements in management. JAMA. 2011;306:294–301.

    Article  PubMed  CAS  Google Scholar 

  5. Soriano V, Pérez-Olmeda M, Ríos P, Núñez M, García-Samaniego J, González-Lahoz J. Hepatitis C virus (HCV) relapses after anti-HCV therapy are more frequent in HIV-infected patients. AIDS Res Hum Retroviruses. 2004;20:351–3.

    Article  PubMed  CAS  Google Scholar 

  6. Medrano J, Barreiro P, Resino S, et al. Rate and timing of hepatitis C virus relapse after a successful course of pegylated interferon plus ribavirin in HIV-infected and HIV-uninfected patients. Clin Infect Dis. 2009;49:1397–401.

    Article  PubMed  CAS  Google Scholar 

  7. Núñez M, Mariño A, Miralles C, et al. Baseline serum hepatitis C virus (HCV) RNA level and response at week 4 are the best predictors of relapse after treatment with pegylated interferon plus ribavirin in HIV/HCV-coinfected patients. J Acquir Immune Defic Syndr. 2007;45:439–44.

    Article  PubMed  Google Scholar 

  8. Ghany MG, Strader DB, Thomas DL, Seeff LB; American Association for the Study of Liver Diseases. Diagnosis, management, and treatment of hepatitis C: an update. AASLD practice guidelines. Hepatology. 2009;49:1335–74.

    Article  PubMed  CAS  Google Scholar 

  9. Centers for Disease Control and Prevention (CDC). Revised surveillance case definitions for HIV infection among adults, adolescents, and children aged <18 months and for HIV infection and AIDS among children aged 18 months to <13 years—United States, 2008. MMWR Recomm Rep. 2008;57:1–8.

    Google Scholar 

  10. Medrano J, Neukam K, Rallón N, et al. Modeling the probability of sustained virological response to therapy with pegylated interferon plus ribavirin in patients coinfected with hepatitis C virus and HIV. Clin Infect Dis. 2010;15:1209–16.

    Article  Google Scholar 

  11. Shirakawa H, Matsumoto A, Joshita S, et al. Pretreatment prediction of virological response to peginterferon plus ribavirin therapy in chronic hepatitis C patients using viral and host factors. Hepatology. 2008;48:1753–60.

    Article  PubMed  CAS  Google Scholar 

  12. Cheng WS, Roberts SK, McCaughan G, et al. Low virological response and high relapse rates in hepatitis C genotype 1 patients with advanced fibrosis despite adequate therapeutic dosing. J Hepatol. 2010;53:616–23.

    Article  PubMed  Google Scholar 

  13. Shin SR, Sinn DH, Gwak GY, et al. Risk factors for relapse in chronic hepatitis C patients who have achieved end of treatment response. J Gastroenterol Hepatol. 2010;25:957–63.

    Article  PubMed  CAS  Google Scholar 

  14. Deschênes M, Bain VG, Lee SS, et al. Identifying HCV genotype 1 patients at risk of relapse. Eur J Gastroenterol Hepatol. 2010;22:546–51.

    Article  PubMed  Google Scholar 

  15. Chung RT, Andersen J, Volberding P, et al. Peginterferon alfa-2a plus ribavirin versus interferon alfa-2a plus ribavirin for chronic hepatitis C in HIV-coinfected persons. N Engl J Med. 2004;351:451–9.

    Article  PubMed  CAS  Google Scholar 

  16. Carrat F, Bani-Sadr F, Pol S, et al. Pegylated interferon alfa-2b vs standard interferon alfa-2b, plus ribavirin, for chronic hepatitis C in HIV-Infected patients: a randomized controlled trial. JAMA. 2004;292:2839–48.

    Article  PubMed  CAS  Google Scholar 

  17. Torriani FJ, Rodriguez-Torres M, Rockstroh JK, et al. Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection in HIV-infected patients. N Engl J Med. 2004;351:438–50.

    Article  PubMed  CAS  Google Scholar 

  18. Rodríguez-Torres M, Ríos-Bedoya CF, Ortiz-Lasanta G, et al. Weight affect relapse rates in latinos with genotype 2/3 chronic hepatitis C (CHC) treated with peg IFN alfa-2a (Pegasys) 180 mcg/week and 800 mg daily of ribavirin for 24 weeks. J Med Virol. 2008;80:1576–80.

    Article  PubMed  Google Scholar 

  19. Jacobson IM, Brown RS Jr, Freilich B, et al. Peginterferon alfa-2b and weight-based or flat-dose ribavirin in chronic hepatitis C patients: a randomized trial. Hepatology. 2007;46:971–81.

    Article  PubMed  CAS  Google Scholar 

  20. Mangia A, Santoro R, Minerva N, et al. Peginterferon alfa-2b and ribavirin for 12 vs. 24 weeks in HCV genotype 2 or 3. N Engl J Med. 2005;352:2609–17.

    Article  PubMed  CAS  Google Scholar 

  21. Jian Wu Y, Shu Chen L, Gui Qiang W. Effects of fatty liver and related factors on the efficacy of combination antiviral therapy in patients with chronic hepatitis C. Liver Int. 2006;26:166–72.

    Article  PubMed  Google Scholar 

  22. Pineda JA, Caruz A, Rivero A, et al. Prediction of response to pegylated interferon plus ribavirin by IL28B gene variation in patients coinfected with HIV and hepatitis C virus. Clin Infect Dis. 2010;51:788–95.

    Article  PubMed  CAS  Google Scholar 

  23. Thompson AJ, Muir AJ, Sulkowski MS, et al. Interleukin-28B polymorphism improves viral kinetics and is the strongest pretreatment predictor of sustained virologic response in genotype 1 hepatitis C virus. Gastroenterology. 2010;139:120–9.

    Article  PubMed  CAS  Google Scholar 

  24. Wiegand J, Neumann K, Böhm S, et al. Prediction of relapse after peginterferon alfa-2b/ribavirin therapy in chronic HCV genotype 1 patients is dependent on minimal residual virema but not on il28b genotype. In: 46th annual meeting of the European Association for the Study of the Liver, Berlin, Germany, March 30–April 3 2011.

  25. Pineda JA, Caruz A, Di Lello FA, et al. Low-density lipoprotein receptor genotyping enhances the predictive value of IL28B genotype in HIV/hepatitis C virus-coinfected patients. AIDS. 2011;25:1415–20.

    Article  PubMed  CAS  Google Scholar 

  26. Grebely J, Pham ST, Matthews GV, et al. Hepatitis C virus reinfection and superinfection among treated and untreated participants with recent infection. Hepatology. 2012;55:1058–69.

    Article  PubMed  CAS  Google Scholar 

  27. van de Laar TJ, Molenkamp R, van den Berg C, et al. Frequent HCV reinfection and superinfection in a cohort of injecting drug users in Amsterdam. J Hepatol. 2009;51:667–74.

    Article  PubMed  Google Scholar 

  28. Poordad F, McCone J Jr, Bacon BR, et al. Boceprevir for untreated chronic HCV genotype 1 infection. N Engl J Med. 2011;364:1195–206.

    Article  PubMed  CAS  Google Scholar 

  29. Jacobson IM, McHutchison JG, Dusheiko G, et al. Telaprevir for previously untreated chronic hepatitis C virus infection. N Engl J Med. 2011;364:2405–16.

    Article  PubMed  CAS  Google Scholar 

  30. Dieterich D, Soriano V, Sherman K, et al. Telaprevir in combination with pegylated interferon-α-2a + ribavirin in HCV/HIV-co-infected patients: a 24-week treatment interim analysis. In: 19th Conference on Retroviruses and Opportunistic Infections (CROI), Seattle, USA, March 2012. Oral abstract 46.

  31. Sulkowski M, Pol S, Cooper C, et al. Boceprevir + pegylated interferon + ribavirin for the treatment of HCV/HIV-co-infected patients: end of treatment (week 48) interim results. In: 19th Conference on Retroviruses and Opportunistic Infections (CROI), Seattle, USA, March 2012. Oral abstract 47.

Download references

Acknowledgments

This work was partly supported by grants from the Fundación Progreso y Salud, Consejería de Salud de la Junta de Andalucía (grants for health research projects, references: 0036/2010, PI-0247-2010 and PI-0208 and 0124/2008) and the Spanish Health Ministry (ISCIII-RETIC RD06/006, and projects PI10/0164 and PI10/01232). A.R. is the recipient of a research extension grant from the Fundación Progreso y Salud, Consejería de Salud de la Junta de Andalucía (reference AI-0011-2010), J.A.P. is the recipient of an extension grant from the Fundación Progreso y Salud of the Consejería de Salud de la Junta de Andalucía (reference AI-0021) and K.N. is the recipient of a Sara Borrell postdoctoral perfection grant from the Instituto de Salud Carlos III (SCO/523/2008).

Conflict of interest

The authors have no conflicts of interest to declare. A.R. has received consulting fees from Bristol-Myers Squibb, Abbott, Gilead, Roche and Boehringer Ingelheim. J.A.P. has received consulting fees from GlaxoSmithKline, Bristol-Myers Squibb, Abbott, Gilead, Merck Sharp & Dohme, Janssen-Cilag and Boehringer Ingelheim. They have received research support from GlaxoSmithKline, Roche, Bristol-Myers Squibb, Schering-Plough, Abbott and Boehringer Ingelheim, and lecture fees from GlaxoSmithKline, Roche, Abbott, Bristol-Myers Squibb, Boehringer Ingelheim and Schering-Plough. The remaining authors have no conflicts of interest to declare.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to A. Rivero-Juarez or A. Rivero.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rivero-Juarez, A., Mira, J.A., Camacho, A. et al. Baseline risk factors for relapse in HIV/HCV co-infected patients treated with PEG-IFN/RBV. Infection 41, 21–26 (2013). https://doi.org/10.1007/s15010-012-0352-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s15010-012-0352-4

Keywords

Navigation