Usefulness of Sofosbuvir and Daclatasvir combination in the treatment of HCV infection in childhood cancer patients: experience from a tertiary care hospital

Uzma Imam, Ait Parkash, Nandlal Daryani, Fahad Mumtaz
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Abstract

Objective: To determine the usefulness of Sofosbuvir-Daclatasvir combination in the treatment of hepatitis c virus infection in paediatric cancer. Method: The retrospective study was conducted at the Oncology Department of the National Institute of Child Health, Karachi, and comprised medical charts of patients who received sofosbuvir and daclatasvir from January 2018 to January 2022. Efficacy was documented by clearance of hepatitis C virus ribonucleic acid as rapid viral response, early viral response and sustained viral response at weeks 4, 12 and 24, respectively. Drug efficacy was determined by monitoring and recording adverse effects. Chemotherapy protocol for the treatment of patients concomitantly receiving direct acting antivirals was modified while looking at drug-drug interactions. The total duration of direct acting antiviral therapy was 12 weeks. Data was analysed using SPSS 24. Results: Of the 804 patients with different malignancies, 132(16.4%) were found positive for hepatitis C virus. Of them, 28(21.21%) patients were started on direct acting antivirals; 17(60.71%) boys and 11(39.28%) girls. The overall mean age was 9.93±6.12 years. The diagnosis was pre-B acute lymphoblastic leukaemia in 18(64.28%) cases, 16(57.14%) were on maintenance chemotherapy, and 18(64.28%) had genotype 1. Pre- and post-treatment mean alanine transaminase levels were 328.00±324.00IU and 36.00±29.00IU, respectively (p=0.003). Pre- and post-treatment mean serum bilirubin levels were 3.13±3.95mg/dl and 0.61±0.21mg/dl (p=0.022). Rapid viral response was achieved in 26(92.85%) children, while early viral response and sustained viral response were achieved in all 28(100%) patients. Minor side effects were noted in 4(14.28%) patients and chemotherapy was continued in all 28(100%) cases as per the designed protocol. Conclusion: The sofosbuvir-daclatasvir combination was found to be effective in hepatitis C virus treatment in paediatric cancer patients. Key Words: Childhood cancer, HCV infection, Direct acting antiviral agents.
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索非布韦和Daclatasvir联合治疗儿童癌症患者HCV感染的有效性:来自三级医院的经验
目的:探讨索非布韦- daclatasvir联合治疗小儿肿瘤丙型肝炎病毒感染的有效性。方法:回顾性研究在卡拉奇国家儿童健康研究所肿瘤科进行,包括2018年1月至2022年1月接受索非布韦和daclatasvir治疗的患者的病历。在第4周、第12周和第24周,丙型肝炎病毒核糖核酸的清除效果分别为快速病毒反应、早期病毒反应和持续病毒反应。通过监测和记录不良反应来确定药物疗效。在观察药物相互作用的同时,对同时接受直接作用抗病毒药物的患者的化疗方案进行了修改。直接抗病毒治疗总持续时间为12周。数据采用SPSS 24进行分析。结果:804例不同恶性肿瘤患者中,丙型肝炎病毒阳性132例(16.4%)。其中28例(21.21%)患者开始使用直接抗病毒药物;男生17例(60.71%),女生11例(39.28%)。总平均年龄为9.93±6.12岁。诊断为b前急性淋巴细胞白血病18例(64.28%),维持化疗16例(57.14%),基因1型18例(64.28%)。治疗前后平均丙氨酸转氨酶水平分别为328.00±324.00IU和36.00±29.00IU (p=0.003)。治疗前后血清胆红素水平分别为3.13±3.95mg/dl和0.61±0.21mg/dl (p=0.022)。26例(92.85%)患儿实现了快速病毒应答,28例(100%)患儿实现了早期病毒应答和持续病毒应答。4例(14.28%)患者出现轻微副作用,所有28例(100%)患者按照设计方案继续化疗。结论:索非布韦-daclatasvir联合治疗小儿肿瘤丙型肝炎是有效的。关键词:儿童癌症,HCV感染,直接抗病毒药物
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