Hepatitis C therapy with direct antiviral agents in patients with advanced chronic kidney disease: real-world experience of the German Hepatitis C-Registry (Deutsches Hepatitis C-Register)

Eur J Gastroenterol Hepatol. 2019 Nov;31(11):1424-1431. doi: 10.1097/MEG.0000000000001426.

Abstract

Background: Direct-acting antiviral agents (DAAs) have revolutionized treatment of chronic hepatitis C in patients with normal glomerular filtration rate (GFR). However, patients with impaired kidney function have been excluded from several clinical trials. We, therefore, investigated the use, effectiveness, and tolerability of DAAs in patients with GFR less than 30 ml/min in the real-world setting.

Patients and methods: An analysis was done within the German Hepatitis C-Registry on 5733 patients including 46 individuals with a baseline GFR less than 30 ml/min treated with sofosbuvir-based (61%) or paritaprevir/ritonavir-based (39%) regimens.

Results: Sustained virological response 12 rates did not differ significantly between patients with baseline GFR less than 30 versus more than 30 ml/min (91 vs. 96%). Nine individuals with a baseline GFR more than 30 ml/min presented with a GFR less than 30 ml/min at the end of treatment. GFR improvement from less than 30 ml/min to more than 30 ml/min was observed in 9/46 cases. Adverse events did not differ in patients with GFR less than 30 versus more than 30 ml/min. However, serious adverse events were significantly more frequent in individuals with GFR less than 30 ml/min and associated with ribavirin.

Conclusion: Different DAA therapies can be safely used with high sustained virological response rates in patients with GFR less than 30 ml/min. Ribavirin has to be avoided because of poor tolerability.

MeSH terms

  • 2-Naphthylamine
  • Acute Disease
  • Adult
  • Aged
  • Anemia / chemically induced
  • Anilides / therapeutic use
  • Antiviral Agents / therapeutic use*
  • Benzimidazoles / therapeutic use
  • Carbamates / therapeutic use
  • Cyclopropanes
  • Disease Progression
  • Drug Therapy, Combination
  • Female
  • Fluorenes / therapeutic use
  • Germany
  • Glomerular Filtration Rate*
  • Hepatitis C, Chronic / blood
  • Hepatitis C, Chronic / complications
  • Hepatitis C, Chronic / drug therapy*
  • Humans
  • Hypertension / chemically induced
  • Imidazoles / therapeutic use
  • Lactams, Macrocyclic
  • Liver Cirrhosis / etiology
  • Macrocyclic Compounds / therapeutic use
  • Male
  • Middle Aged
  • Pleural Effusion / chemically induced
  • Proline / analogs & derivatives
  • Pyrrolidines
  • RNA, Viral / blood
  • Registries
  • Renal Insufficiency, Chronic / complications
  • Renal Insufficiency, Chronic / metabolism*
  • Ribavirin / therapeutic use
  • Ritonavir / therapeutic use
  • Severity of Illness Index
  • Simeprevir / therapeutic use
  • Sofosbuvir / therapeutic use
  • Sulfonamides / therapeutic use
  • Sustained Virologic Response
  • Treatment Outcome
  • Uracil / analogs & derivatives
  • Uracil / therapeutic use
  • Uridine Monophosphate / analogs & derivatives
  • Uridine Monophosphate / therapeutic use
  • Valine / analogs & derivatives

Substances

  • Anilides
  • Antiviral Agents
  • Benzimidazoles
  • Carbamates
  • Cyclopropanes
  • Fluorenes
  • Imidazoles
  • Lactams, Macrocyclic
  • Macrocyclic Compounds
  • Pyrrolidines
  • RNA, Viral
  • Sulfonamides
  • ledipasvir, sofosbuvir drug combination
  • ombitasvir
  • Ribavirin
  • Uracil
  • Proline
  • Simeprevir
  • 2-Naphthylamine
  • dasabuvir
  • Uridine Monophosphate
  • Valine
  • daclatasvir
  • Ritonavir
  • paritaprevir
  • Sofosbuvir