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Hepatitis C Virus Treatment Response to Ledipasvir/Sofosbuvir Among Patients Co-Infected with HIV and HCV: Real-world Data in a Black Population
BACKGROUND: Treatment of Hepatitis C virus (HCV) infection for patients with Human Immunodeficiency Virus (HIV) has improved with direct acting antivirals (DAAs). However, outcomes among Black persons treated with ledipasvir/sofosbuvir (LDV/SOF) may be inferior to non-Blacks. We assessed responses t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630883/ http://dx.doi.org/10.1093/ofid/ofx163.1754 |
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author | Banga, Jaspreet Nizami, Sobia Slim, Jihad Nagarakanti, Sandhya Portilla, Mario Swaminathan, Shobha |
author_facet | Banga, Jaspreet Nizami, Sobia Slim, Jihad Nagarakanti, Sandhya Portilla, Mario Swaminathan, Shobha |
author_sort | Banga, Jaspreet |
collection | PubMed |
description | BACKGROUND: Treatment of Hepatitis C virus (HCV) infection for patients with Human Immunodeficiency Virus (HIV) has improved with direct acting antivirals (DAAs). However, outcomes among Black persons treated with ledipasvir/sofosbuvir (LDV/SOF) may be inferior to non-Blacks. We assessed responses to LDV/SOF in a cohort of Black HIV/HCV co-infected persons in Newark, New Jersey. METHODS: Retrospective chart reviews were conducted for Black, genotype 1 (GT1), HIV/HCV co-infected patients treated with LDV/SOF at three hospitals in Newark, New Jersey between January 2014 and July 2016. Data collected included demographics, HCV treatment history, treatment duration and response. RESULTS: 117 HIV/HCV co-infected Black patients started treatment with LDV/SOF but 5 had no follow up data and 5 prematurely discontinued treatment (1 due to side effects). We included 107 HIV/HCV co-infected patients who completed LDV/SOF at all three sites. The study population was 65% male, median age 58 years, 26% had cirrhosis and 77% had GT1a. 31% were treatment experienced but none with prior NS5a treatment. At baseline, median CD4 count was 680 cells/mm(3), HIV viral load (VL) was < 40 in 94% and median HCV VL was 2257403 IU/ml. 29% of patients changed antiretroviral treatment (ART) before LDV/SOF treatment due to drug interactions (Table-1). CONCLUSION: In this real-world cohort of Black, GT1, HIV/HCV co-infected patients, LDV/SOF had high SVR12 rate of 93%. However, there were not enough patients in the 8 week arm to assess its efficacy. This data supports the overall high efficacy of LDV/SOF in a difficult-to-treat patient population. DISCLOSURES: J. Slim, Gilead: CME/CE, Consultant, Investigator and Speaker’s Bureau, Consulting fee, Research support and Speaker honorarium; Abbvie: CME/CE, Consultant and Investigator, Consulting fee, Research support and Speaker honorarium; Merck: CME/CE, Consultant and Investigator, Consulting fee, Research support and Speaker honorarium; ViiV: CME/CE, Consultant and Investigator, Consulting fee, Research support and Speaker honorarium; Janssen: CME/CE and Consultant, Consulting fee and Speaker honorarium; BMS: CME/CE, Speaker honorarium S. Swaminathan, Gilead Sciences: Grant Investigator and Scientific Advisor, Consulting fee and Research grant |
format | Online Article Text |
id | pubmed-5630883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56308832017-11-07 Hepatitis C Virus Treatment Response to Ledipasvir/Sofosbuvir Among Patients Co-Infected with HIV and HCV: Real-world Data in a Black Population Banga, Jaspreet Nizami, Sobia Slim, Jihad Nagarakanti, Sandhya Portilla, Mario Swaminathan, Shobha Open Forum Infect Dis Abstracts BACKGROUND: Treatment of Hepatitis C virus (HCV) infection for patients with Human Immunodeficiency Virus (HIV) has improved with direct acting antivirals (DAAs). However, outcomes among Black persons treated with ledipasvir/sofosbuvir (LDV/SOF) may be inferior to non-Blacks. We assessed responses to LDV/SOF in a cohort of Black HIV/HCV co-infected persons in Newark, New Jersey. METHODS: Retrospective chart reviews were conducted for Black, genotype 1 (GT1), HIV/HCV co-infected patients treated with LDV/SOF at three hospitals in Newark, New Jersey between January 2014 and July 2016. Data collected included demographics, HCV treatment history, treatment duration and response. RESULTS: 117 HIV/HCV co-infected Black patients started treatment with LDV/SOF but 5 had no follow up data and 5 prematurely discontinued treatment (1 due to side effects). We included 107 HIV/HCV co-infected patients who completed LDV/SOF at all three sites. The study population was 65% male, median age 58 years, 26% had cirrhosis and 77% had GT1a. 31% were treatment experienced but none with prior NS5a treatment. At baseline, median CD4 count was 680 cells/mm(3), HIV viral load (VL) was < 40 in 94% and median HCV VL was 2257403 IU/ml. 29% of patients changed antiretroviral treatment (ART) before LDV/SOF treatment due to drug interactions (Table-1). CONCLUSION: In this real-world cohort of Black, GT1, HIV/HCV co-infected patients, LDV/SOF had high SVR12 rate of 93%. However, there were not enough patients in the 8 week arm to assess its efficacy. This data supports the overall high efficacy of LDV/SOF in a difficult-to-treat patient population. DISCLOSURES: J. Slim, Gilead: CME/CE, Consultant, Investigator and Speaker’s Bureau, Consulting fee, Research support and Speaker honorarium; Abbvie: CME/CE, Consultant and Investigator, Consulting fee, Research support and Speaker honorarium; Merck: CME/CE, Consultant and Investigator, Consulting fee, Research support and Speaker honorarium; ViiV: CME/CE, Consultant and Investigator, Consulting fee, Research support and Speaker honorarium; Janssen: CME/CE and Consultant, Consulting fee and Speaker honorarium; BMS: CME/CE, Speaker honorarium S. Swaminathan, Gilead Sciences: Grant Investigator and Scientific Advisor, Consulting fee and Research grant Oxford University Press 2017-10-04 /pmc/articles/PMC5630883/ http://dx.doi.org/10.1093/ofid/ofx163.1754 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Banga, Jaspreet Nizami, Sobia Slim, Jihad Nagarakanti, Sandhya Portilla, Mario Swaminathan, Shobha Hepatitis C Virus Treatment Response to Ledipasvir/Sofosbuvir Among Patients Co-Infected with HIV and HCV: Real-world Data in a Black Population |
title | Hepatitis C Virus Treatment Response to Ledipasvir/Sofosbuvir Among Patients Co-Infected with HIV and HCV: Real-world Data in a Black Population |
title_full | Hepatitis C Virus Treatment Response to Ledipasvir/Sofosbuvir Among Patients Co-Infected with HIV and HCV: Real-world Data in a Black Population |
title_fullStr | Hepatitis C Virus Treatment Response to Ledipasvir/Sofosbuvir Among Patients Co-Infected with HIV and HCV: Real-world Data in a Black Population |
title_full_unstemmed | Hepatitis C Virus Treatment Response to Ledipasvir/Sofosbuvir Among Patients Co-Infected with HIV and HCV: Real-world Data in a Black Population |
title_short | Hepatitis C Virus Treatment Response to Ledipasvir/Sofosbuvir Among Patients Co-Infected with HIV and HCV: Real-world Data in a Black Population |
title_sort | hepatitis c virus treatment response to ledipasvir/sofosbuvir among patients co-infected with hiv and hcv: real-world data in a black population |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630883/ http://dx.doi.org/10.1093/ofid/ofx163.1754 |
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