Sofosbuvir, ribavirin and pegylated interferon for a daclatasvir-resistent genotype 3 hepatitis C virus

case report and review

  • Marcos Mucenic Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Ajacio Bandeira de Melo Brandão Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Claudio Augusto Marroni Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Alfeu de Medeiros Fleck Junior Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Maria Lucia Zanotelli Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Ian Leipnitz Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Mário Henrique Meine Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Guillermo Kiss Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Juliano Martini Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Eduardo Soares Schlindwein Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Ane Micheli Costabeber Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Fernanda Karlinsky Rodrigues Sacco Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Giovana Rossato Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
  • Guido Pio Cracco Cantisani Irmandade Santa Casa de Misericórdia de Porto Alegre, Grupo de Transplante Hepático
Keywords: Hepatitis C virus, Liver transplantation, Treatment

Abstract

Chronic Hepatitis C relapse after liver transplantation can lead to graft failure within a short time period. The high efficacy and good safety profile of direct-acting antivirals has led to consensual recommendations for using interferon-free treatment after liver transplantation. However, pegylated interferon may still be required for genotype 3 non-responders. We treated a liver graft recipient with grade 1 fibrosis in the biopsy with daclatasvir and sofosbuvir for 12 weeks. He did not respond and progressed to grade 3 fibrosis. Lacking other options, we obtained a sustained virological response with pegylated interferon, ribavirin and sofosbuvir for 12 weeks. The combination of pegylated interferon, ribavirin and sofosbuvir is a viable option after the failure of direct acting antivirals in economically disadvantaged countries.

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Published
2019-02-07
How to Cite
Mucenic, M., Brandão, A., Marroni, C. A., Fleck Junior, A., Zanotelli, M. L., Leipnitz, I., Meine, M. H., Kiss, G., Martini, J., Schlindwein, E., Costabeber, A., Sacco, F., Rossato, G., & Cantisani, G. (2019). Sofosbuvir, ribavirin and pegylated interferon for a daclatasvir-resistent genotype 3 hepatitis C virus. Revista Do Instituto De Medicina Tropical De São Paulo, 61, e12. https://doi.org/10.1590/S1678-9946201961012
Section
Case Report

INTRODUCTION

Chronic Hepatitis C Virus (HCV) infection is one of the most common diagnoses in candidates for liver transplantation (LT) throughout the world. HCV relapses in more than two thirds of those recipients that still have detectable viremia when they are submitted to LT. Furthermore, they have much higher viral loads and an accelerated disease course in the setting of immunosuppression1.

The high efficacy and good safety profile of direct-acting antivirals (DAA) has led to consensual recommendations for using interferon-free treatment after LT2-4. However, there are very few options for patients who fail to respond to DAA, especially in developing countries where newer drugs are not yet available. We report the case of DAA failure after LT with successful retreatment using pegylated interferon with ribavirin (PR) and sofosbuvir, and review the pertinent literature.

CASE PRESENTATION

We describe the case of a male patient submitted to LT due to hepatocellular carcinoma (HCC) and compensated cirrhosis caused by HCV when he was 67 years old. The HCC had been treated with alcohol injections and was completely necrotic on the liver explant. He had failed to respond to treatment twice before LT, once with standard interferon and ribavirin and once with PR. On the 17th postoperative month, he began a 48-week course of PR. Viremia lowered from 3 million international units (IU) to 92 IU at treatment week 12. It was undetectable at week 24 and at the end of treatment, but he suffered a relapse 6 months later, with a viral load of approximately 1 million IU. PR caused mild pleural and pericardial effusion and mild ascites, leading to the interruption of these drugs at week 48 instead of 72. Liver biopsy results are shown in Table 1. Four years and 3 months after LT, he was treated with daclatasvir and sofosbuvir for 12 weeks according to the Brazilians’ public health protocol at that time, which restricted treatment duration to 12 weeks for all patients. Notwithstanding, post-treatment viral load was 580.000 IU. One year after that, a fibroelastogram showed a liver stiffness of 9.6 kPa, equivalent to grade 3 fibrosis. Two different liver ultrasound examinations did not disclose any signs of chronic liver disease or portal hypertension. The patient then received PR plus sofosbuvir for 12 weeks. The viral load fell to 35 IU after 4 weeks of treatment. Within 7 weeks, ribavirin had to be reduced from 1 g to 500 mg daily, because serum hemoglobin fell from 12.8 to 7.6 mg/dL. He received two red blood cell transfusions; ribavirin was reduced to 250 mg per day, which he was able to receive until the end of treatment. Viral load was undetectable (less than 12 IU/mL) 24 weeks after treatment and remained so when tested after another year.

Table 1:
Anatomopathological results of liver biopsies.
Postoperative Time Inflammation Fibrosis Conclusion
6 months Severe (grade 3) Absent Acute hepatitis C
9 months Moderate (grade 2) Mild (grade 1) Chronic hepatitis C Metavir A2F1
48 months Mild (grade 1) Mild (grade 1) Chronic hepatitis C Metavir A1F1

DISCUSSION

The benefits of treating HCV relapse after LT have been more thoroughly evaluated with interferon. There is progression to cirrhosis in more than 20% of patients in 5 years without treatment , with a minimum decompensation rate of 30% in the first year. Sustained virological response (SVR) leads to favorable outcome with improvement of fibrosis, graft and patient survival and reduced rates of decompensated cirrhosis5-8.

DAA have revolutionized HCV treatment by means of high efficacy and a favorable safety profile. In Brazil, DAA has been provided by the public health system since 2015. We have only two options available for the treatment of genotype 3 HCV: PR plus sofosbuvir or sofosbuvir plus daclatasvir, with the possibility of adding ribavirin, for 12 or 24 weeks. At the time the reported patient was treated, there was no recommendation from the Brazilian public health system to use ribavirin in all LT patients.

Genotype 3 HCV is associated with fewer treatment options, faster rates of progression to fibrosis and lower SVR rates, especially in the presence of advanced fibrosis or decompensated cirrhosis9. Due to its lower prevalence, it was underrepresented in clinical trials, especially those that included LT patients10-14.

We have previously published our real-life data on HCV treatment after LT with a 12-week course of sofosbuvir and daclatasvir, with or without ribavirin. There were 4 treatment failures in 39 patients (89.7% SVR) and one of them is the case reported here. It is worth noticing that all failures occurred in the subgroup of 26 patients with genotype 3 HCV15. The CUPILT study included 137 mono-infected HCV LT patients treated with sofosbuvir and daclatasvir, with or without ribavirin, but only 15 patients were genotype 316. Ally-1 Phase 3 trial is currently underway and its preliminary results have shown up to 91% of SVR rates, but genotype 3 was represented by only 11 of 53 LT recipients treated with a 12-week course of sofosbuvir, daclatasvir and ribavirin17.

Considering the accelerated rate of progression to fibrosis in these immunocompromised patients, they should be treated without delay, using other classes of drugs. Current options for retreating DAA-experienced genotype 3 patients include combinations such as sofosbuvir, velpatasvir and voxilaprevir18, glecaprevir and pibrentasvir or triple combinations including these drugs19. However, these recently released DAA are still unavailable in many countries.

Resistance-associated variants (RAVs) are selected when treatment with daclatasvir or other nonstructural protein 5A (NS5A) inhibitors fails, and they might persist for a long time after treatment discontinuation1. RAVs can compromise DAA retreatment results with regimens that include NS5A inhibitors. On the other hand, the Y93H RAV has been shown to increase susceptibility to interferon-based therapy in comparison with the Y93 wild type, favoring interferon-containing regimens in these cases20.

Unlike NS5A inhibitors such as daclatasvir, sofosbuvir is a NS5B polymerase inhibitor with a high genetic barrier to resistance. A sofosbuvir and PR combination was recommended in EASL and AASLD editions in 2015 for genotype 3 HCV infection, excluding patients with decompensated cirrhosis and LT recipients3,4. The TARGET real-life study included a subgroup of 19 patients that received PR plus sofosbuvir with 84% SVR, although most of them were genotype 1 with no history of LT21. Although it is not a currently recommended option after LT, there is a large experience with PR treatment in these patients before DAAs were available.

The therapeutic success that we obtained in this case is relevant, because it shows there is an economically viable option for LT patients, in whom the disease can progress too rapidly to wait for new drugs to become available in countries that cannot afford to distribute the top line DAA treatment.

REFERENCES

  1. , , (). Recurrent hepatitis C after liver transplant. World J Gastroenterol 20, 10668-10681.
  2. , , , , , (). ELITA consensus statements on the use of DAAs in liver transplant candidates and recipients. J Hepatol 67, 585-602.
  3. (). EASL Recommendations on Treatment of Hepatitis C 2015. J Hepatol 63, 199-236.
  4. (). Hepatitis C guidance: AASLD-IDSA recommendations for testing, managing, and treating adults infected with hepatitis C virus. Hepatology 62, 932-954.
  5. , , , , , (). Sustained viral response to interferon and ribavirin in liver transplant recipients with recurrent hepatitis C. Liver Transpl 10, 199-207.
  6. , , , , , (). Benefit of sustained virological response to combination therapy on graft survival of liver transplanted patients with recurrent chronic hepatitis C. Am J Transplant 5, 1909-1913.
  7. , , , , , (). Impact of pegylated interferon and ribavirin treatment on graft survival in liver transplant patients with recurrent hepatitis C infection. Am J Transplant 8, 2426-2433.
  8. , , , , , (). Antiviral treatment of recurrent hepatitis C after liver transplantation: predictors of response and long-term outcome. Transplantation 88, 1214-1221.
  9. , , , , , (). Genotype 3 is associated with accelerated fibrosis progression in chronic hepatitis C. J Hepatol 51, 655-666.
  10. , , , (). Interferon-free hepatitis C treatment before and after liver transplantation: the role of HCV drug resistance. Viruses 7, 5155-5168.
  11. , , , , , (). Sofosbuvir and ribavirin for treatment of compensated recurrent hepatitis C virus infection after liver transplantation. Gastroenterology 148, 108-117.
  12. , , , , , (). An interferon-free antiviral regimen for HCV after liver transplantation. N Engl J Med 371, 2375-2382.
  13. , , , , , (). Multicenter experience using simeprevir and sofosbuvir with or without ribavirin to treat hepatitis C genotype 1 after liver transplant. Hepatology 61, 1880-1886.
  14. , , , , , (). Sofosbuvir plus daclatasvir for post-transplant recurrent hepatitis C: potent antiviral activity but no clinical benefit if treatment is given late. Dig Liv Dis 46, 923-927.
  15. , , , , , (). Daclatasvir and sofosbuvir with or without ribavirin in liver transplant recipients: a single-center real-world study. Transplant Proc 50, 769-771.
  16. , , , , , (). Multicentre experience using daclatasvir and sofosbuvir to treat hepatitis C recurrence – The ANRS CUPILT study. J Hepatol 65, 711-718.
  17. , , , , , (). Daclatasvir, sofosbuvir, and ribavirin combination for HCV patients with advanced cirrhosis or posttransplant recurrence: phase 3 ALLY-1 study. J Hepatol 62, S261-S262.
  18. , , , , , (). Sofosbuvir, velpatasvir, and voxilaprevir for previously treated HCV infection. N Engl J Med 376, 2134-2146.
  19. (). EASL Recommendations on Treatment of Hepatitis C 2018. J Hepatol 69, 461-511.
  20. , , , , , (). Resistance-associated NS5A variants of hepatitis C virus are susceptible to interferon-based therapy. PloS One 10
  21. , , , , , (). Effectiveness and safety of sofosbuvir-based regimens for chronic HCV genotype 3 infection: results of the HCV-TARGET Study. Clin Infect Dis 63, 776-783.