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基于面板的基因组检测在转移性结直肠癌治疗决策中的真实世界成本效益。

Real-world cost-effectiveness of panel-based genomic testing to inform therapeutic decisions for metastatic colorectal cancer.

机构信息

Canadian Centre for Applied Research in Cancer Control, Canada; Cancer Control Research, BC Cancer, Vancouver, BC, Canada.

Canadian Centre for Applied Research in Cancer Control, Canada; Cancer Control Research, BC Cancer, Vancouver, BC, Canada.

出版信息

J Cancer Policy. 2024 Sep;41:100496. doi: 10.1016/j.jcpo.2024.100496. Epub 2024 Jul 18.

Abstract

BACKGROUND

Mutations in KRAS and NRAS are associated with a lack of response to cetuximab and panitumumab, two biologics used for third-line therapy of metastatic colorectal cancer (mCRC). In British Columbia, Canada, eligibility for cetuximab or panitumumab was first based on single-gene KRAS testing. OncoPanel, a multi-gene next-generation sequencing panel with both KRAS and NRAS, was introduced in 2016. Our objective was to estimate the real-world cost-effectiveness of OncoPanel versus to single-gene KRAS testing to inform eligibility for cetuximab or panitumumab in mCRC.

METHODS

Using population-based administrative health data, we identified a cohort of mCRC patients who had received a KRAS or OncoPanel test, and completed prior chemotherapy in 2010-2019. We matched KRAS- and OncoPanel-tested patients (1:1) using genetic matching to balance baseline covariates. Mean and incremental 3-year costs, survival, and quality-adjusted survival were estimated using inverse-probability-of-censoring weighting and bootstrapping. We conducted scenario-based sensitivity analysis for key costs and assumptions.

FINDINGS

All OncoPanel-tested cases (n=371) were matched to a KRAS-tested comparator. In the KRAS and OncoPanel groups, respectively, 55·8 % and 41·2 % of patients were potentially eligible for cetuximab or panitumumab based on mutation status. Incremental cost and effectiveness of OncoPanel were $72 (95 % CI: -6387, 6107), -0·004 life-years (95 % CI: -0·119, 0·113), and -0·011 quality-adjusted life-years (95 % CI: -0·094, 0·075). Reductions in systemic therapy costs were offset by increased costs in other resources. Results were moderately sensitive to time horizon and changes in testing or treatment cost.

INTERPRETATION

The use of OncoPanel resulted in more precise targeting of cetuximab and panitumumab, but there was no change in incremental cost or quality-adjusted survival. Understanding the balance of costs achieved in practice can provide insight into the effect of future changes in testing policy, test cost, treatment eligibility, or drug prices in this setting.

摘要

背景

KRAS 和 NRAS 突变与西妥昔单抗和帕尼单抗(两种用于转移性结直肠癌(mCRC)三线治疗的生物制剂)无应答相关。在加拿大不列颠哥伦比亚省,西妥昔单抗或帕尼单抗的使用资格最初基于单基因 KRAS 检测。OncoPanel 是一种具有 KRAS 和 NRAS 的多基因下一代测序面板,于 2016 年推出。我们的目的是评估 OncoPanel 与单基因 KRAS 检测相比在 mCRC 中用于确定西妥昔单抗或帕尼单抗使用资格的真实世界成本效益。

方法

使用基于人群的行政健康数据,我们确定了一组在 2010-2019 年间接受过 KRAS 或 OncoPanel 检测且已完成先前化疗的 mCRC 患者。我们使用遗传匹配对 KRAS 检测和 OncoPanel 检测的患者(1:1)进行匹配,以平衡基线协变量。使用逆概率删失加权和自举法估计 3 年的平均和增量成本、生存和质量调整生存。我们对关键成本和假设进行了基于情景的敏感性分析。

结果

所有 OncoPanel 检测的病例(n=371)均与 KRAS 检测的对照组相匹配。在 KRAS 和 OncoPanel 组中,分别有 55.8%和 41.2%的患者根据突变状态可能有资格使用西妥昔单抗或帕尼单抗。OncoPanel 的增量成本和效果分别为 72 美元(95%CI:-6387,6107)、0.004 个生命年(95%CI:-0.119,0.113)和 0.011 个质量调整生命年(95%CI:-0.094,0.075)。系统治疗成本的降低被其他资源成本的增加所抵消。结果对时间范围和检测或治疗成本的变化具有中等敏感性。

解释

OncoPanel 的使用使得西妥昔单抗和帕尼单抗的靶向性更加精确,但增量成本或质量调整后的生存没有变化。了解在实践中实现的成本平衡可以深入了解未来检测政策、检测成本、治疗资格或药物价格变化对该环境的影响。

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