期刊
CURRENT ONCOLOGY
卷 26, 期 5, 页码 E597-E609出版社
MDPI
DOI: 10.3747/co.26.4843
关键词
Cost-effectiveness analyses; EGFR inhibitors; primary tumour location; RAS wild-type; colorectal cancer; metastatic
类别
资金
- Ontario Ministry of Research, Innovation, and Science Early Researcher Award
- Natural Sciences and Engineering Research Council of Canada
- Canadian Institutes of Health Research
Background Evidence from a retrospective analysis of multiple large phase III trials suggested that primary tumour location (PTL) in RAS wild-type metastatic colorectal cancer (wtRAS mcRC) might have predictive value with respect to response to drug therapies. Recent studies also show a potential preferential benefit for epidermal growth factor inhibitors (EGFRis) for left-sided tumours. In the present study, we aimed to determine the incremental cost-effectiveness ratio (ICER) for the first-line use of an EGFRi for patients with left-sided wtRAS mcRC. Methods We developed a state-transition model to determine the cost effectiveness of alternative treatment strategies in patients with left-sided mcRC: Standard of care Use of an EGFRi in first-line therapy The cohort for the study consisted of patients diagnosed with unresectable wtRAS mcRC with an indication for chemotherapy and previously documented PTL. Model parameters were obtained from the published literature and calibration. The perspective was that of a provincial ministry of health in Canada. We used a 5-year time horizon and an annual discount rate of 1.5%. Results Selecting patients for first-line EGFRi treatment based on left-sided location of their colorectal primary tumour was more effective than the standard of care, resulting in an increase in quality-adjusted life-years (QALYS) of 0.226 (or 0.644 life-years gained). However, the strategy was also more expensive, costing an average of $60,639 more per patient treated. The resulting ICER was $268,094 per QALY. A 35% price reduction in the cost of EGFRi would be needed to make this strategy cost-effective at a willingness-to-pay threshold (WTP) of $100,000 per QALY. Conclusions Selective use of an EGFRi based on PTL was more cost-effective than unselected use of those agents; however, based on traditional WTP thresholds, it was still not cost-effective. While awaiting the elucidation of more precise predictive biomarkers that might improve cost-effectiveness, the price of EGFRis could be reduced to meet the WTP threshold.
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