National Centre in HIV Epidemiology and Clinical Research, University of New South Wales, Sydney, Australia.
J Hepatol. 2011 Jul;55(1):76-85. doi: 10.1016/j.jhep.2010.10.033. Epub 2010 Nov 23.
BACKGROUND & AIMS: Adherence to HCV therapy impacts sustained virological response (SVR) but there are limited data on adherence, particularly among injecting drug users (IDUs). We assessed 80/80 adherence (≥80% of PEG-IFN doses, ≥80% treatment), on-treatment adherence, and treatment completion in a study of treatment of recent HCV infection (ATAHC).
Participants with HCV received pegylated interferon (PEG-IFN) alfa-2a (180μg/week, n=74) and those with HCV/HIV received PEG-IFN alfa-2a with ribavirin (n=35), for a planned 24 weeks. Logistic regression analyses were used to identify predictors of PEG-IFN 80/80 adherence.
A total of 109 out of 163 patients received treatment (HCV, n=74; HCV/HIV, n=35), with 75% ever reporting IDU. The proportion with 80/80 PEG-IFN adherence was 82% (n=89). During treatment, 14% missed ≥1 dose (on-treatment adherence=99%). Completion of 0-4, 5-19, 20-23, and all 24 weeks of PEG-IFN therapy occurred in 10% (n=11), 14% (n=15), 6% (n=7) and 70% (n=76) of cases, respectively. Participants with no tertiary education were less likely to have 80/80 PEG-IFN adherence (AOR 0.29, p=0.045). IDU prior to or during treatment did not impact 80/80 PEG-IFN adherence. SVR was higher among those patients with ≥80/80 PEG-IFN adherence (67% vs. 35%, p=0.007), but similar among those with and without missed doses during therapy (73% vs. 60%, p=0.309). SVR in those patients discontinuing therapy between 0-4, 5-19, 20-23, and 24 weeks was 9%, 33%, 43%, and 76%, respectively (p<0.001).
High adherence to treatment for recent HCV was observed, irrespective of IDU prior to, or during, therapy. Sub-optimal PEG-IFN exposure was mainly driven by early treatment discontinuation rather than missed doses during therapy.
对 HCV 治疗的依从性会影响持续病毒学应答(SVR),但目前关于依从性的数据有限,尤其是在注射吸毒者(IDU)中。我们评估了最近 HCV 感染治疗研究(ATAHC)中 80/80 依从性(≥80%PEG-IFN 剂量,≥80%治疗)、治疗期间依从性和治疗完成情况。
接受聚乙二醇干扰素(PEG-IFN)α-2a(180μg/周,n=74)治疗的 HCV 患者和接受 HCV/HIV 治疗的患者接受 PEG-IFNα-2a 联合利巴韦林(n=35)治疗,计划治疗 24 周。采用 logistic 回归分析确定 PEG-IFN 80/80 依从性的预测因素。
在 163 名患者中,共有 109 名接受了治疗(HCV,n=74;HCV/HIV,n=35),其中 75%曾报告有 IDU。80/80PEG-IFN 依从性的比例为 82%(n=89)。在治疗期间,有 14%的患者漏用了≥1 剂(治疗期间依从性=99%)。完成 0-4、5-19、20-23 和全部 24 周 PEG-IFN 治疗的比例分别为 10%(n=11)、14%(n=15)、6%(n=7)和 70%(n=76)。未接受过高等教育的参与者不太可能达到 80/80PEG-IFN 依从性(AOR 0.29,p=0.045)。在治疗前或治疗期间有 IDU 并不影响 80/80PEG-IFN 依从性。≥80/80PEG-IFN 依从性的患者 SVR 更高(67% vs. 35%,p=0.007),但在治疗期间漏用药物的患者中 SVR 相似(73% vs. 60%,p=0.309)。在 0-4、5-19、20-23 和 24 周之间停药的患者的 SVR 分别为 9%、33%、43%和 76%(p<0.001)。
观察到最近 HCV 治疗的高依从性,无论 IDU 在治疗前还是治疗期间。PEG-IFN 暴露不足主要是由于早期停药而不是治疗期间漏用药物所致。