Direct-acting antiviral regimens in Egyptian patients with chronic hepatitis C virus infection: A real-world single-center experience

被引:8
|
作者
Naguib, Gina Gamal [1 ]
Farid, Amir [2 ]
Hassan, Mohamed [1 ,3 ]
Elshafie, Ahmed [1 ,3 ]
El Shazly, Yehia [1 ]
Shaker, Mohamed Kamal [2 ]
Ezzat, Haitham [1 ]
Safwat, Eslam [1 ]
Ahmed, Ossama Ashraf [1 ]
Dabbous, Hany [2 ]
Sherief, Ahmed Fouad [2 ]
Hassany, Mohamed [4 ]
Elserafy, Magdy [5 ]
Elsayed, Manal Hamdy [6 ,7 ]
机构
[1] Ain Shams Univ, Fac Med, Dept Internal Med, Cairo, Egypt
[2] Ain Shams Univ, Dept Trop Med & Infect Dis, Cairo, Egypt
[3] Armed Forces Coll Med, Cairo Governorate, Egypt
[4] Natl Hepatol & Trop Med Res Inst, Dept Trop Med, Cairo, Egypt
[5] Cairo Univ, Dept Trop Med, Fac Med, Giza, Egypt
[6] Ain Shams Univ, Fac Med, Dept Pediat, Cairo, Egypt
[7] Ain Shams Univ, Fac Med, Clin Res Ctr, Cairo, Egypt
关键词
Direct-acting antiviral; Interferon-free regimen; Hepatitis C virus; GENOTYPE; 1; PATIENTS; SAFETY; LEDIPASVIR/SOFOSBUVIR; SOFOSBUVIR; RIBAVIRIN; DASABUVIR; OMBITASVIR; VETERANS; PROGRAM; SVR;
D O I
10.1016/j.ajg.2021.06.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and study aims:: Chronic hepatitis C virus (HCV) infection has always been identified as a major health threat and a potential cause of liver cirrhosis, portal hypertension, and other associated problems. The introduction of direct-acting antiviral agents (DAAs) has represented a paradigm shift in HCV management. In this study, we aim to observe the rate of sustained virologic response (SVR12) in a large scale of patients at a single center as well as record the post-treatment changes in the hematologic, hepatic, and renal biochemical profiles. Patients and methods: In total, 1933 chronic HCV genotype 4 mono-infected non-HCC patients who completed the treatment with six different DAA regimens in the Faculty of Medicine, Ain Shams University Research Institute (MASRI), were retrospectively enrolled in this study. The rate of sustained virologic response after 12 weeks off-therapy (SVR12) was assessed. The baseline characteristics to predict the SVR12 were then analyzed. The post-treatment changes in many profiles were recorded and analyzed. Results: The overall SVR12 rate was 96.2% (after excluding 84 cases who were lost to follow-up). It was achieved in 346/375 patients (92.3%), 466/477 patients (97.7%), 60/62 patients (96.8%), 11/11 patients (100%), 532/545 patients (97.6%), and 445/463 patients (96.1%) who received sofosbuvir/daclatasvir (SOF/DCV), sofosbuvir/daclatasvir/ribavirin (SOF/DCV/RBV), sofosbuvir/ledipasvir (SOF/LDV), sofosbuvir/ledipasvir/ribavirin (SOF/LDV/RBV), sofosbuvir/simeprevir (SOF/SMV), and ombitasvir/parita previr/ritonavir/ribavirin (OBV/PTV/r + RBV), respectively. In total, 73 patients (3.8%) failed to achieve SVR12. The baseline aspartate aminotransferase (AST), cirrhotic status, and treatment regimen were determined to have a significant impact on SVR12. In the overall treated population, the levels of serum AST, alanine aminotransferase, albumin, creatinine, bilirubin, and hemoglobin and platelet count improved significantly after treatment. Furthermore, sustained virologic response was strongly related to cirrhosis and its degree. Conclusion: The interferon-free DAA regimens offered high SVR12 rates in Egyptian patients with chronic HCV infection. They were associated with a significant improvement in the hematologic, hepatic, and renal biochemical profiles. The baseline AST, liver cirrhosis, and treatment regimen might have an impact on achieving SVR. (c) 2021 Pan-Arab Association of Gastroenterology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:285 / 291
页数:7
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