Mason Neil T, Burkett Jason M, Nelson Ryan S, Pow-Sang Julio M, Gatenby Robert A, Kubal Timothy, Peabody John W, Letson G Douglas, McLeod Howard L, Zhang Jingsong
Personalized Medicine Strategist, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Manager, Payer Strategies Analytics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
Am Health Drug Benefits. 2021 Mar;14(1):15-20.
The use of a novel strategy known as adaptive abiraterone therapy based on mathematical modeling of evolutionary dynamics of tumor subpopulations was shown in a clinical trial to extend the time to disease progression in patients with metastatic castration-resistant prostate cancer (CRPC) and reduced the use of abiraterone therapy. Although the clinical impact of adaptive abiraterone treatment is clear, the economic impact of this strategy has not been investigated.
To compare the cost of care with adaptive abiraterone therapy versus standard continuous abiraterone therapy in patients with metastatic CRPC, using patient billing data.
We performed a retrospective review of billing data for patients with metastatic CRPC who received abiraterone treatment at a large cancer center between June 1, 2012, and August 31, 2018. Patients were divided into 2 groups based on whether they received adaptive abiraterone therapy (N = 15) or continuous abiraterone therapy (N = 21). All patients with refractory, metastatic prostate cancer after castration that was indicated for abiraterone therapy were eligible for this study. Each patient in the adaptive abiraterone therapy cohort received abiraterone plus prednisone treatment until the patient reached a target threshold of 50% or more reduction in prostate-specific antigen (PSA) level compared with his PSA level before abiraterone therapy; treatment was then suspended until the PSA level rose above the 50% of PSA before abiraterone therapy target threshold. The continuous therapy cohort received abiraterone plus prednisone daily until radiographic progression. The primary outcomes were the mean annual cost of care per patient, including and excluding the cost of abiraterone, and the cost of care, by clinical category.
The median time to disease progression was 25.8 months for patients who received adaptive abiraterone therapy compared with 12.1 months for patients who received continuous abiraterone therapy. Overall, the mean total, including the cost of drug, annual cost per patient who received adaptive abiraterone therapy was $79,093 compared with $146,782 for patients who received continuous abiraterone therapy ( <.0001). The annual cost of care per patient, excluding the cost of abiraterone, was $13,883 for those who received adaptive therapy versus $22,322 for those who received continuous abiraterone therapy ( = .2757), which was not statistically significant.
Practical precision medicine strategies, such as adaptive abiraterone treatment or pharmacogenomics-targeted dosing, can use known biomarkers, such as PSA, to tailor therapy, generate improved outcomes, and reduce costs without the need for novel drug and diagnostic discovery and development. The results of this study suggest that a large clinical study of adaptive abiraterone therapy is warranted to validate the potential of this strategy to extend the time to disease progression and reduce costs of treatment of metastatic CRPC.
在一项临床试验中,基于肿瘤亚群进化动力学数学模型的新型策略——适应性阿比特龙疗法,被证明可延长转移性去势抵抗性前列腺癌(CRPC)患者的疾病进展时间,并减少阿比特龙疗法的使用。尽管适应性阿比特龙治疗的临床影响已很明确,但该策略的经济影响尚未得到研究。
利用患者计费数据,比较转移性CRPC患者接受适应性阿比特龙疗法与标准持续阿比特龙疗法的护理成本。
我们对2012年6月1日至2018年8月31日期间在一家大型癌症中心接受阿比特龙治疗的转移性CRPC患者的计费数据进行了回顾性分析。根据患者接受的是适应性阿比特龙疗法(N = 15)还是持续阿比特龙疗法(N = 21)将患者分为两组。所有因去势后难治性转移性前列腺癌而适合接受阿比特龙治疗的患者均符合本研究条件。适应性阿比特龙疗法队列中的每位患者接受阿比特龙加泼尼松治疗,直到患者的前列腺特异性抗原(PSA)水平相较于阿比特龙治疗前的水平降低50%或更多,达到目标阈值;然后暂停治疗,直到PSA水平升至阿比特龙治疗前PSA的50%目标阈值以上。持续治疗队列每天接受阿比特龙加泼尼松治疗,直至影像学进展。主要结局是每位患者的年均护理成本,包括和不包括阿比特龙成本,以及按临床类别划分的护理成本。
接受适应性阿比特龙疗法的患者疾病进展的中位时间为25.8个月,而接受持续阿比特龙疗法的患者为12.1个月。总体而言,接受适应性阿比特龙疗法的患者平均总年度成本(包括药物成本)为79,093美元,而接受持续阿比特龙疗法的患者为146,782美元(P <.0001)。接受适应性疗法的患者每位患者的年均护理成本(不包括阿比特龙成本)为13,883美元,而接受持续阿比特龙疗法的患者为22,322美元(P = 0.2757),无统计学意义。
实用的精准医学策略,如适应性阿比特龙治疗或药物基因组学靶向给药,可以利用已知生物标志物,如PSA,来调整治疗方案,改善治疗效果并降低成本,而无需进行新药和诊断的发现与开发。本研究结果表明,有必要对适应性阿比特龙疗法进行大规模临床研究,以验证该策略延长疾病进展时间和降低转移性CRPC治疗成本的潜力。