Department of Radiology, Brigham and Women's Hospital, Boston, Massachusetts.
Institute for Technology Assessment, Massachusetts General Hospital, Boston, Massachusetts.
J Thorac Oncol. 2020 Aug;15(8):1298-1305. doi: 10.1016/j.jtho.2020.03.001. Epub 2020 Apr 6.
To evaluate the cost-effectiveness of a number of follow-up guidelines and variants for subsolid pulmonary nodules.
We used a simulation model informed by data from the literature and the National Lung Screening Trial to simulate patients with ground-glass nodules (GGNs) detected at baseline computed tomography undergoing follow-up. The nodules were allowed to grow and develop solid components over time. We tested the guidelines generated by varying follow-up recommendations for low-risk nodules, that is, pure GGNs or those stable over time. For each guideline, we computed average US costs and quality-adjusted life-years (QALYs) gained per patient and identified the incremental cost-effectiveness ratios of those on the efficient frontier. In addition, we compared the costs and effects of the most recently released version of the Lung Computed Tomography Screening Reporting and Data System (Lung-RADS), version 1.1, with those of the previous version, 1.0. Finally, we performed sensitivity analyses of our results by varying several relevant parameters.
Relative to the no follow-up scenario, the follow-up guideline system that was cost-effective at a willingness-to-pay of $100,000/QALY and had the greatest QALY assigned low-risk nodules a 2-year follow-up interval and stopped follow-up after 2 years for GGNs and after 5 years for part-solid nodules; this strategy yielded an incremental cost-effectiveness ratio of $99,970. Lung-RADS version 1.1 was found to be less costly but no less effective than Lung-RADS version 1.0. These findings were essentially stable under a range of sensitivity analyses.
Ceasing follow-up for low-risk subsolid nodules after 2 to 5 years of stability is more cost-effective than perpetual follow-up. Lung-RADS version 1.1 was cheaper but similarly effective to version 1.0.
评估多种亚实性肺结节随访指南和方案的成本效益。
我们使用基于文献和国家肺癌筛查试验数据的模拟模型来模拟基线计算机断层扫描检测到磨玻璃结节(GGN)的患者进行随访。随着时间的推移,结节允许生长并发展为实性成分。我们通过改变低风险结节(即纯 GGN 或随时间稳定的结节)的随访建议来测试指南。对于每个指南,我们计算了每位患者的平均超声检查成本和获得的质量调整生命年(QALY),并确定了有效边界上的增量成本效益比。此外,我们比较了最新发布的肺计算机断层扫描筛查报告和数据系统(Lung-RADS)版本 1.1 与前一版本 1.0 的成本和效果。最后,我们通过改变几个相关参数对结果进行了敏感性分析。
与不随访方案相比,在愿意支付 100,000 美元/QALY 的情况下具有成本效益且分配给低风险结节的 QALY 最大的随访指南系统为低风险 GGN 结节分配了 2 年的随访间隔,并在 2 年后停止随访,在 5 年后停止随访对于部分实性结节;该策略的增量成本效益比为 99,970 美元。发现 Lung-RADS 版本 1.1 的成本低于版本 1.0,但效果相同。在一系列敏感性分析中,这些发现基本保持稳定。
对于稳定 2 至 5 年的低风险亚实性结节,停止随访比持续随访更具成本效益。Lung-RADS 版本 1.1 更便宜,但与版本 1.0 同样有效。