Kircher Sheetal M, Mohindra Nisha, Nimeiri Halla
Department of Medicine, Division of Hematology-Oncology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA
Department of Medicine, Division of Hematology-Oncology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Oncologist. 2015 Jan;20(1):14-8. doi: 10.1634/theoncologist.2014-0252. Epub 2014 Nov 19.
In colorectal cancer (CRC), evidence shows that expanding RAS testing to analyze more mutations may better predict benefit from anti-EGFR therapy. The economic implications of expanding RAS testing for metastatic CRC were analyzed.
Estimates of standard KRAS exon 2 testing were based on the Centers for Medicare and Medicaid Services (CMS) 2014 Diagnostic Laboratory Fee Schedule, and expanded RAS testing was estimated using a sensitivity analysis done with various potential cost scenarios (1, 2, 10, and 30 times the cost of the standard KRAS test). The cost estimates for cetuximab and panitumumab were based on the CMS payment allowance limits for Medicare Part B.
A total of 28,692 patients with metastatic CRC were estimated to be eligible annually for RAS testing. For cetuximab, the societal cost of standard KRAS testing plus the drug versus expanded testing plus the drug would be $1.16 billion versus $816 million if the cost of the tests were the same. If the cost of the expanded RAS test were 30 times the cost of the standard test, then the societal cost of standard KRAS testing plus the drug versus expanded testing plus the drug would be $1.16 billion versus $980 million, a continued savings of more than $184 million annually. Similar savings were seen with panitumumab.
The increased societal cost of expanded RAS testing versus standard approved KRAS exon 2 testing was inconsequential when compared with the amount of money saved by not treating the additional 18% of patients who harbor additional RAS mutations (beyond exon 2) with anti-EGFR therapy.
在结直肠癌(CRC)中,有证据表明扩大RAS检测以分析更多突变可能能更好地预测抗表皮生长因子受体(EGFR)治疗的获益情况。本研究分析了扩大转移性结直肠癌RAS检测的经济影响。
标准KRAS外显子2检测的费用估算基于医疗保险和医疗补助服务中心(CMS)2014年诊断实验室收费表,扩大RAS检测则通过对各种潜在成本情景(标准KRAS检测成本的1倍、2倍、10倍和30倍)进行敏感性分析来估算。西妥昔单抗和帕尼单抗的成本估算基于医疗保险B部分的CMS支付限额。
估计每年共有28,692例转移性结直肠癌患者符合RAS检测条件。对于西妥昔单抗,如果检测成本相同,标准KRAS检测加药物的社会成本与扩大检测加药物的社会成本分别为11.6亿美元和8.16亿美元。如果扩大RAS检测的成本是标准检测成本的30倍,那么标准KRAS检测加药物的社会成本与扩大检测加药物的社会成本分别为11.6亿美元和9.8亿美元,每年仍可节省超过1.84亿美元。帕尼单抗也有类似的节省情况。
与不对另外18%携带额外RAS突变(外显子2以外)的患者进行抗EGFR治疗所节省的费用相比,扩大RAS检测相对于标准的KRAS外显子2检测增加的社会成本微不足道。