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Impact of CD4+ T-cell count on sustained virologic response to direct-acting antivirals in hepatitis C virus monoinfected cancer patients: a prospective observational study.
- Source :
-
Diagnostic microbiology and infectious disease [Diagn Microbiol Infect Dis] 2022 Jul; Vol. 103 (3), pp. 115719. Date of Electronic Publication: 2022 May 04. - Publication Year :
- 2022
-
Abstract
- Limited data are available on the use of CD4+ T-cell count and percentage to predict response to direct-acting antiviral (DAA) treatment outside the hepatitis C virus (HCV)-HIV coinfected population. We sought to determine the impact of CD4+ T-cell count and percentage on response to DAAs in cancer patients with HCV monoinfection. Patients treated with DAAs were enrolled in a prospective observational study. CD4+ T-cell count and percentage was measured at baseline, end of treatment (EOT), and 12 weeks after the EOT (SVR12). A total of 174 patients were enrolled. Most patients (155/174, 89%) achieved an SVR12. A multivariate logistic regression model found that patients with hepatocellular carcinoma, HCV-3 and previous DAA treatment were more likely to develop treatment failure. Neither univariate analysis nor multivariate logistic regression analysis did show any association between CD4+ T-cell count or percentage and SVR12. CD4 T-cell count or percentage does not appear to impact SVR rates in cancer patients with HCV monoinfection receiving DAAs.<br /> (Copyright © 2022 Elsevier Inc. All rights reserved.)
- Subjects :
- Antiviral Agents therapeutic use
CD4-Positive T-Lymphocytes
Hepacivirus
Humans
Sustained Virologic Response
Treatment Outcome
HIV Infections complications
HIV Infections drug therapy
HIV Infections epidemiology
Hepatitis C
Hepatitis C, Chronic complications
Hepatitis C, Chronic drug therapy
Neoplasms complications
Neoplasms drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0070
- Volume :
- 103
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Diagnostic microbiology and infectious disease
- Publication Type :
- Academic Journal
- Accession number :
- 35605562
- Full Text :
- https://doi.org/10.1016/j.diagmicrobio.2022.115719