Assessment of direct-acting antiviral treatment outcomes in patients with chronic hepatitis C infected with various HCV genotypes: Insights from a real-world cohort in West Bengal, India.

IF 3 3区 医学 Q2 INFECTIOUS DISEASES
Supradip Dutta, Shreyasi Nath, Raina Das, Sagnik Bakshi, Moumita Majumdar, Anwesha Ghosh, Upasana Baskey, Prosanto Kumar Chowdhury, Provash Chandra Sadhukhan
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引用次数: 0

Abstract

Background & objectives: Genomic diversity of Hepatitis C Virus (HCV), accessibility and long-term influence of Direct Acting Antiviral (DAA) treatment remain underexplored among HCV-infected chronic liver disease (CLD) patients in the real world. This retrospective study addressed the inadequacy of assessing the effectiveness of DAA and identify genotype-specific variations in treatment response in the context of HCV epidemiology. Additionally, real-world treatment challenges encountered during the COVID-19 pandemic and the transitional phase of implementing the National Viral Hepatitis Control Program (NVHCP) guidelines have also been addressed.

Methods: This retrospective study included 254 CLD patients from November 2017 and February 2020 to assess the effectiveness of DAA and long-term treatment outcomes among CLD patients.

Results: HCV viremia was observed in 58.26% (n = 148) patients. Patients aged 52-59 years with a history of blood transfusions exhibited a higher prevalence of active HCV infection. Two major genotypes (GT) - GT1 and GT3, and seven subtypes with few new subtypes were identified. SVR24 was achieved in 89.6% of patients receiving sofosbuvir (SOF) + daclatasvir (DCV) or SOF/ledipasvir (LDV) drug regimens. For individuals who failed to reach SVR24 (n = 13), a modified regimen (SOF + Velpatasvir (VEL) + ribavirin (Riba) for 6 months) was given and the success rate was 92.31%. GT-1a and GT-1b showed better treatment response, whereas GT-3b had a lower treatment response. Among 77 SVR24 achieved patients, 57.14% were cirrhotic and 42.86% were non-cirrhotic at the start of the therapy.

Interpretation & conclusion: This study highlights genotype-specific variations in treatment response, with GT-3b exhibiting lower treatment response which highlights the need to decipher the reasons behind treatment failure for future therapeutic management.

评估不同HCV基因型感染的慢性丙型肝炎患者的直接抗病毒治疗结果:来自印度西孟加拉邦现实世界队列的见解
背景与目的:在现实世界中,丙型肝炎病毒(HCV)的基因组多样性、直接抗病毒药物(DAA)治疗的可及性和长期影响在丙型肝炎感染的慢性肝病(CLD)患者中仍未得到充分探讨。本回顾性研究解决了在HCV流行病学背景下评估DAA有效性和确定治疗反应基因型特异性差异的不足。此外,在COVID-19大流行期间和实施国家病毒性肝炎控制规划(NVHCP)指南的过渡阶段遇到的现实治疗挑战也得到了解决。方法:本回顾性研究纳入2017年11月至2020年2月的254例CLD患者,以评估DAA的有效性和CLD患者的长期治疗结果。结果:HCV病毒血症发生率为58.26% (n = 148)。52-59岁有输血史的患者表现出较高的活动性HCV感染患病率。主要基因型(GT)为GT1和GT3,并鉴定出7个亚型,新增亚型较少。在接受索非布韦(SOF) + daclatasvir (DCV)或SOF/ledipasvir (LDV)药物方案的患者中,89.6%的患者达到了SVR24。对于未达到SVR24的患者(n = 13),给予改良方案(SOF +维帕他韦(VEL) +利巴韦林(Riba) 6个月),成功率为92.31%。GT-1a和GT-1b的治疗反应较好,而GT-3b的治疗反应较低。在77例获得SVR24治疗的患者中,治疗开始时57.14%为肝硬化,42.86%为非肝硬化。解释和结论:本研究强调了治疗反应的基因型特异性差异,GT-3b表现出较低的治疗反应,这表明需要破译治疗失败背后的原因,以便未来的治疗管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
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