首页> 外文期刊>Journal of community genetics >Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care
【24h】

Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care

机译:基于研究的综合基因组测序在先进癌症治疗中的早期经济分析

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Genomic research is driving discovery for future population benefit. Limited evidence exists on immediate patient and health system impacts of research participation. This study uses real-world data and quasi-experimental matching to examine early-stage cost and health impacts of research-based genomic sequencing. British Columbia's Personalized OncoGenomics (POG) single-arm program applies whole genome and transcriptome analysis (WGTA) to characterize genomic landscapes in advanced cancers. Our cohort includes POG patients enrolled between 2014 and 2015 and 1:1 genetic algorithm-matched usual care controls. We undertake a cost consequence analysis and estimate 1-year effects of WGTA on patient management, patient survival, and health system costs reported in 2015 Canadian dollars. WGTA costs are imputed and forecast using system of equations modeling. We use Kaplan-Meier survival analysis to explore survival differences and inverse probability of censoring weighted linear regression to estimate mean 1-year survival times and costs. Non-parametric bootstrapping simulates sampling distributions and enables scenario analysis, revealing drivers of incremental costs, survival, and net monetary benefit for assumed willingness to pay thresholds. We identified 230 POG patients and 230 matched controls for cohort inclusion. The mean period cost of research-funded WGTA was $26,211 (SD: $14,191). Sequencing costs declined rapidly, with WGTA forecasts hitting $13,741 in 2021. The incremental healthcare system effect (non-research expenditures) was $5203 (95 CI: 75, 10,424) compared to usual care. No overall survival differences were observed, but outcome heterogeneity was present. POG patients receiving WGTA-informed treatment experienced incremental survival gains of 2.49 months (95 CI: 1.32, 3.64). Future cost consequences became favorable as WGTA cost drivers declined and WGTA-informed treatment rates improved to 60. Our study demonstrates the ability of real-world data to support evaluations of only-in-research health technologies. We identify situations where precision oncology research initiatives may produce survival benefit at a cost that is within healthcare systems' willingness to pay. This economic evidence informs the early-stage healthcare impacts of precision oncology research.
机译:基因组研究正在推动未来人口造福的发现。关于参与研究对患者和卫生系统的直接影响的证据有限。本研究使用真实世界数据和准实验匹配来检查基于研究的基因组测序的早期成本和健康影响。不列颠哥伦比亚省的个性化肿瘤基因组学 (POG) 单臂项目应用全基因组和转录组分析 (WGTA) 来表征晚期癌症的基因组景观。我们的队列包括 2014 年至 2015 年间入组的 POG 患者和 1:1 遗传算法匹配的常规护理对照。我们进行了成本后果分析,并估计了 WGTA 对患者管理、患者生存和卫生系统成本的 1 年影响,以 2015 年加元计算。WGTA成本使用方程组建模进行估算和预测。我们使用 Kaplan-Meier 生存分析来探索生存差异和删失加权线性回归的逆概率,以估计平均 1 年生存时间和成本。非参数引导模拟抽样分布并实现情景分析,揭示假设支付意愿阈值的增量成本、生存和净货币收益的驱动因素。我们确定了 230 名 POG 患者和 230 名匹配的对照组纳入队列。研究资助的WGTA的平均期间成本为26,211美元(SD:14,191美元)。测序成本迅速下降,WGTA 预测 2021 年将达到 13,741 美元。与常规护理相比,医疗保健系统增量效应(非研究支出)为5203美元(95%CI:75,10,424)。未观察到总生存差异,但存在结局异质性。接受WGTA知情治疗的POG患者的生存期增量为2.49个月(95%CI:1.32,3.64)。随着WGTA成本驱动因素的下降和WGTA知情治疗率提高到60%,未来的成本后果变得有利。我们的研究表明,真实世界的数据能够支持对仅在研究中的卫生技术的评估。我们确定了精准肿瘤学研究计划可能以医疗保健系统愿意支付的成本产生生存益处的情况。这一经济证据为精准肿瘤学研究的早期医疗保健影响提供了信息。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号