Puri Pankaj, Saraswat Vivek A, Dhiman Radha K, Anand Anil C, Acharya Subrat K, Singh Shivaram P, Chawla Yogesh K, Amarapurkar Deepak N, Kumar Ajay, Arora Anil, Dixit Vinod K, Koshy Abraham, Sood Ajit, Duseja Ajay, Kapoor Dharmesh, Madan Kaushal, Srivastava Anshu, Kumar Ashish, Wadhawan Manav, Goel Amit, Verma Abhai, Pandey Gaurav, Malik Rohan, Agrawal Swastik
Department of Internal Medicine, Armed Forces Medical College, Pune 411040, India.
Department of Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow 226014, India.
J Clin Exp Hepatol. 2016 Jun;6(2):119-45. doi: 10.1016/j.jceh.2016.07.001. Epub 2016 Jul 2.
India contributes significantly to the global burden of HCV. While the nucleoside NS5B inhibitor sofosbuvir became available in the Indian market in March 2015, the other directly acting agents (DAAs), Ledipasvir and Daclatasvir, have only recently become available in the India. The introduction of these DAA in India at a relatively affordable price has led to great optimism about prospects of cure for these patients as not only will they provide higher efficacy, but combination DAAs as all-oral regimen will result in lower side effects than were seen with pegylated interferon alfa and ribavirin therapy. Availability of these newer DAAs has necessitated revision of INASL guidelines for the treatment of HCV published in 2015. Current considerations for the treatment of HCV in India include the poorer response of genotype 3, nonavailability of many of the DAAs recommended by other guidelines and the cost of therapy. The availability of combination DAA therapy has simplified therapy of HCV with decreased reliance of evaluation for monitoring viral kinetics or drug related side effects.
印度对全球丙型肝炎病毒(HCV)负担有重大影响。虽然核苷类NS5B抑制剂索磷布韦于2015年3月在印度市场上市,但其他直接抗病毒药物(DAAs),如来迪派韦和达卡他韦,直到最近才在印度上市。这些DAA以相对可承受的价格在印度推出,这让人们对治愈这些患者的前景充满了极大的乐观情绪,因为它们不仅疗效更高,而且作为全口服方案的联合DAA比聚乙二醇化干扰素α和利巴韦林疗法的副作用更低。这些更新的DAA的出现使得有必要修订印度肝脏研究学会(INASL)于2015年发布的HCV治疗指南。目前印度治疗HCV的考虑因素包括3型基因型反应较差、其他指南推荐的许多DAA无法获得以及治疗费用。联合DAA疗法的出现简化了HCV治疗,减少了对监测病毒动力学或药物相关副作用评估的依赖。