Chiu Richard, Tatara Eric, Mackesy-Amiti Mary Ellen, Page Kimberly, Ozik Jonathan, Boodram Basmattee, Dahari Harel, Gutfraind Alexander
Department of Medicine, University of Illinois College of Medicine at Chicago, Chicago, IL 60612, USA.
The Program for Experimental & Theoretical Modeling, Department of Medicine, Division of Hepatology, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60660, USA.
Healthcare (Basel). 2024 Mar 13;12(6):644. doi: 10.3390/healthcare12060644.
Despite the availability of direct-acting antivirals that cure individuals infected with the hepatitis C virus (HCV), developing a vaccine is critically needed in achieving HCV elimination. HCV vaccine trials have been performed in populations with high incidence of new HCV infection such as people who inject drugs (PWID). Developing strategies of optimal recruitment of PWID for HCV vaccine trials could reduce sample size, follow-up costs and disparities in enrollment. We investigate trial recruitment informed by machine learning and evaluate a strategy for HCV vaccine trials termed PREDICTEE-Predictive Recruitment and Enrichment method balancing Demographics and Incidence for Clinical Trial Equity and Efficiency. PREDICTEE utilizes a survival analysis model applied to trial candidates, considering their demographic and injection characteristics to predict the candidate's probability of HCV infection during the trial. The decision to recruit considers both the candidate's predicted incidence and demographic characteristics such as age, sex, and race. We evaluated PREDICTEE using in silico methods, in which we first generated a synthetic candidate pool and their respective HCV infection events using HepCEP, a validated agent-based simulation model of HCV transmission among PWID in metropolitan Chicago. We then compared PREDICTEE to conventional recruitment of high-risk PWID who share drugs or injection equipment in terms of sample size and recruitment equity, with the latter measured by participation-to-prevalence ratio (PPR) across age, sex, and race. Comparing conventional recruitment to PREDICTEE found a reduction in sample size from 802 (95%: 642-1010) to 278 (95%: 264-294) with PREDICTEE, while also reducing screening requirements by 30%. Simultaneously, PPR increased from 0.475 (95%: 0.356-0.568) to 0.754 (95%: 0.685-0.834). Even when targeting a dissimilar maximally balanced population in which achieving recruitment equity would be more difficult, PREDICTEE is able to reduce sample size from 802 (95%: 642-1010) to 304 (95%: 288-322) while improving PPR to 0.807 (95%: 0.792-0.821). PREDICTEE presents a promising strategy for HCV clinical trial recruitment, achieving sample size reduction while improving recruitment equity.
尽管有可治愈丙型肝炎病毒(HCV)感染者的直接抗病毒药物,但开发一种疫苗对于实现消除HCV至关重要。HCV疫苗试验已在新HCV感染高发人群中进行,如注射毒品者(PWID)。制定针对HCV疫苗试验的PWID最佳招募策略可以减少样本量、随访成本以及招募方面的差异。我们研究了由机器学习提供信息的试验招募情况,并评估了一种用于HCV疫苗试验的策略,称为PREDICTEE——平衡人口统计学和发病率以实现临床试验公平与效率的预测性招募和富集方法。PREDICTEE利用应用于试验候选者的生存分析模型,考虑他们的人口统计学和注射特征来预测候选者在试验期间感染HCV的概率。招募决策同时考虑候选者的预测发病率和年龄、性别、种族等人口统计学特征。我们使用计算机模拟方法评估了PREDICTEE,其中我们首先使用HepCEP生成了一个合成候选者库及其各自的HCV感染事件,HepCEP是一个经过验证的基于主体的芝加哥大都市PWID中HCV传播模拟模型。然后我们将PREDICTEE与传统的招募共用毒品或注射设备的高风险PWID的方法在样本量和招募公平性方面进行了比较,后者通过年龄、性别和种族的参与率与患病率之比(PPR)来衡量。将传统招募方法与PREDICTEE进行比较发现,使用PREDICTEE时样本量从802(95%:642 - 1010)减少到278(95%:264 - 294),同时筛查要求降低了30%。同时,PPR从0.475(95%:0.356 - 0.568)提高到0.754(95%:0.685 - 0.834)。即使针对一个更难实现招募公平的不同的最大平衡人群,PREDICTEE也能够将样本量从802(95%:642 - 1010)减少到304(95%:288 - 322),同时将PPR提高到0.807(95%:0.792 - 0.821)。PREDICTEE为HCV临床试验招募提供了一种有前景的策略,在减少样本量的同时提高了招募公平性。