Safety and efficacy of Sofosbuvir and Velpatasvir in children with active hepatitis C virus infection undergoing haploidentical transplantation.
Sarita Rani JaiswalPrakash BhakuniMayank SoniMahesh GuptaAtul ThataiSuparno ChakrabartiPublished in: Transplant infectious disease : an official journal of the Transplantation Society (2020)
Direct Acting Antivirals (DAA) have changed the landscape of hepatitis C virus (HCV) infection with high cure rates across genotypes. However, the use of these agents in the setting of allogeneic hematopoietic cell transplantation (HCT) has been limited. In this context, we report the outcome of five children (5-12 years) with relapsed and refractory leukemia and active HCV infection (genotype 1b), who underwent urgent haploidentical HCT and were treated with Sofosbuvir and Velpatasvir (Sof-Vel) from initiation of treatment to 24 weeks post-HCT. All achieved complete virologic response (VR) at a median of 2 weeks, with normalization of liver enzymes. There were no adverse events related to the use of Sof-Vel, with no major fluctuations in cyclosporine levels. Two of the patients developed chronic GVHD and one relapsed. Sof-Vel was continued in one of them along with sirolimus without affecting drug levels. With a median follow-up of 15 months, four patients are disease free with sustained VR. Our study shows that combination of Sof-Vel might be effective in inducing rapid complete and sustained VR during HCT without any major untoward drug interaction.
Keyphrases
- hepatitis c virus
- end stage renal disease
- stem cell transplantation
- bone marrow
- hepatitis c virus infection
- acute myeloid leukemia
- newly diagnosed
- human immunodeficiency virus
- ejection fraction
- acute lymphoblastic leukemia
- chronic kidney disease
- prognostic factors
- young adults
- stem cells
- diffuse large b cell lymphoma
- peritoneal dialysis
- emergency department
- cell cycle arrest
- drug induced
- allogeneic hematopoietic stem cell transplantation
- low dose
- high dose
- multiple myeloma
- peripheral blood
- mesenchymal stem cells
- hiv infected
- single cell
- pi k akt
- adverse drug