Yi Shana, Truong David, Conway Brian
Vancouver Infectious Diseases Center, Vancouver, British Columbia, Canada.
Health Sciences, Simon Fraser University, Burnaby, British Columbia, Canada.
J Virus Erad. 2024 Dec 3;10(4):100569. doi: 10.1016/j.jve.2024.100569. eCollection 2024 Dec.
Several clinical trials, including the recently published the GRAND PLAN study from Vancouver Infectious Diseases Center (VIDC), have demonstrated the efficacy of hepatitis C (HCV) therapy among active drug users, including those facing significant addiction-related and social challenges. In the GRAND PLAN, we documented sustained virological response post-treatment Week12 (SVR12) in 108/117 (92.3 %) individuals (108/111 (mITT) or 97.3 % of those reaching the SVR12 timepoint) receiving an 8-week course of glecaprevir/pibrentasvir (G/P), with almost all using fentanyl and over half being unstably housed. Data on the maintenance of this favorable outcome in the long-term in such a population with a significant risk of reinfection is limited. We hypothesized that the offer of ongoing multidisciplinary care (including addiction care) after SVR12 was achieved would reduce the likelihood of loss to follow up, HCV reinfection or death and consolidate the gains achieved by initial engagement in care to diagnose and treat HCV infection.
The inception cohort for this analysis was the 108 individuals achieving a cure of HCV infection within the GRAND PLAN study. All were offered the opportunity to continue to receive care at the VIDC. This is a multidisciplinary model of care to address medical, mental health, social and addiction-related concerns on an ongoing basis. This included, if necessary, opiate agonist and safer supply therapy, usually provided by the pharmacy adjacent to our inner-city campus. Among those choosing to be retained in care, the endpoint of this analysis was loss to follow up, mortality and HCV reinfection and their correlates. Reinfection was ascertained by repeat HCV RNA testing every 6 months, more frequently if clinically indicated.
Of the 108 individuals making up the inception cohort for this analysis, all chose to remain in care at the VIDC. We note a median age of 47 (22-75) years, 28 % female, 21.3 % identifying as indigenous, the majority with mild fibrosis (90.8 % F0-F2), slightly more than half with unstable housing. It is of note that we recorded a 20 % decrease in fentanyl users among those who were cured compared to the baseline evaluation of the overall study cohort (73.5 % vs 94.9 %, p < 0.000001). Among the cured individuals, 104 (96.3 %) remained alive, while 4 individuals died of opioid overdoses. Out of the 104 , 99 (95.2 %) remained HCV-free, while 5 (4.8 %) were re-infected. All five have recently initiated repeat HCV therapy at VIDC, 2 of whom are already documented to be cured.
Among a population of vulnerable inner-city residents cured of HCV infection within a multidisciplinary program of care at the VIDC, all individuals accepted the offer to remain in long-term follow up, with a statistically significant reduction in fentanyl use over time. In the setting of an ongoing opioid crisis where 3 deaths/day are recorded in the neighborhood where the study population resides, we documented 4 deaths. Reinfections occurred at a very modest rate, with maintenance in care allowing prompt re-treatment, with a cure already being documented in 2/5 cases, with the other 3 individuals remaining on HCV therapy at the VIDC.
包括温哥华传染病中心(VIDC)最近发表的GRAND PLAN研究在内的多项临床试验,已证明丙型肝炎(HCV)治疗在活跃吸毒者中的疗效,包括那些面临重大成瘾相关和社会挑战的人。在GRAND PLAN研究中,我们记录了108/117(92.3%)的个体在接受为期8周的glecaprevir/pibrentasvir(G/P)治疗后第12周实现持续病毒学应答(SVR12)(108/111(mITT),即达到SVR12时间点的个体中的97.3%),几乎所有人都使用芬太尼,超过一半的人居住不稳定。关于在这样一个有显著再感染风险的人群中长期维持这一良好结果的数据有限。我们假设,在实现SVR12后提供持续的多学科护理(包括成瘾护理)将降低失访、HCV再感染或死亡的可能性,并巩固通过最初参与护理来诊断和治疗HCV感染所取得的成果。
本分析的初始队列是GRAND PLAN研究中108例实现HCV感染治愈的个体。所有人都有机会继续在VIDC接受护理。这是一种多学科护理模式,旨在持续解决医疗、心理健康、社会和成瘾相关问题。如有必要,这包括阿片类激动剂和更安全供应治疗,通常由我们市中心校区附近的药房提供。在选择继续接受护理的人中,本分析的终点是失访、死亡率和HCV再感染及其相关因素。通过每6个月重复进行HCV RNA检测来确定再感染,如果临床有指征则检测更频繁。
在构成本分析初始队列的108例个体中,所有人都选择继续在VIDC接受护理。我们注意到中位年龄为47(22 - 75)岁,28%为女性,21.3%为原住民,大多数为轻度纤维化(90.8% F0 - F2),略超过一半的人居住不稳定。值得注意的是,与整个研究队列的基线评估相比,我们记录到治愈者中芬太尼使用者减少了20%(73.5%对94.9%,p < 0.000001)。在治愈的个体中,104例(96.3%)存活,4例死于阿片类药物过量。在这104例中,99例(95.2%)保持无HCV状态,而5例(4.8%)再次感染。所有5例最近都在VIDC开始了重复HCV治疗,其中2例已记录治愈。
在VIDC多学科护理项目中治愈HCV感染的弱势市中心居民群体中,所有个体都接受了继续长期随访的提议,随着时间推移芬太尼使用量有统计学意义的下降。在研究人群居住的社区每天有3人死于阿片类药物过量的持续阿片类药物危机背景下,我们记录到4例死亡。再感染发生率非常低,持续接受护理允许及时重新治疗,2/5的病例已记录治愈,另外3例个体仍在VIDC接受HCV治疗。