National Cancer Institute, Division of Cancer Control and Population Sciences, Surveillance Research Program, Rockville, MD.
National Cancer Institute, Division of Cancer Control and Population Sciences, Health Care Delivery Research Program, Rockville, MD.
J Manag Care Spec Pharm. 2020 Dec;26(12):1494-1504. doi: 10.18553/jmcp.2020.26.12.1494.
Following approval of imatinib, a breakthrough tyrosine kinase inhibitor (TKI), survival significantly improved by more than 20% since 2001 among treated chronic myelogenous leukemia (CML) patients. Subsequently, more expensive second-generation TKIs with varying selectivity profiles have been approved. Population-based studies are needed to evaluate the real-world utilization of TKI therapies, particularly given their escalating costs and recommendations for maintenance therapy. To assess the utilization patterns of first-line TKIs, overall and by specific agent, among elderly CML patients in the United States, and the cost implications. CML patients aged 65 years and older at diagnosis between 2007 and 2015 were identified from population-based cancer registries in the linked Surveillance, Epidemiology, and End Results (SEER)-Medicare database. The percentage of CML patients receiving imatinib, dasatinib, or nilotinib within the first year of diagnosis was calculated along with time to first-line treatment initiation. Bivariate comparisons and Cox proportional hazards models were used to identify factors associated with TKI initiation. Average monthly patient responsibility, including patient out-of-pocket (OOP) costs, stratified by Part D low-income subsidy (LIS) status were also calculated. Among the 1,589 CML patients included, receipt of any TKI within 1 year of diagnosis increased from 66.2% to 78.9%. In 2015, the distribution of first-line TKI therapies was 41.3% imatinib, 28.3% dasatinib, and 9.3% nilotinib. Almost 60% of patients initiated TKI treatment within 3 months of diagnosis. Multivariable analysis indicated that TKI use in the first year was lower among the very elderly (aged > 75 years vs. 65-69 years: HR = 0.72; 95% CI = 0.63-0.83), patients with more comorbidities (Hierarchical Condition Category risk score > 2 vs. HR = 0.74, 95% CI = 0.62-0.88), and patients ineligible for LIS (HR = 0.75; 95% CI = 0.65-0.87). Average monthly patient OOP cost was significantly lower for LIS-eligible versus LIS-ineligible patients: imatinib (2016: $12 vs. $487), dasatinib (2016: $34 vs. $557), and nilotinib (2016: $1 vs. $526). TKI use has increased significantly since 2007. While imatinib remained the most frequently prescribed first-line agent, by 2015 newer TKIs represented one third of the market share. Utilization patterns indicated persistent age, comorbidity, and financial barriers. TKI use is indicated for long-term therapy, and increased adoption of newer, more expensive agents raises concerns about the sustained affordability of CML treatment, particularly among unsubsidized patients. No outside funding supported this study. There are no reported conflicts of interest.
伊马替尼获批后,自 2001 年以来,接受治疗的慢性髓性白血病(CML)患者的生存率提高了 20%以上。随后,批准了具有不同选择性特征的更昂贵的第二代 TKI。需要进行基于人群的研究来评估 TKI 治疗的实际应用情况,特别是考虑到其成本不断上升和维持治疗的建议。本研究旨在评估美国老年 CML 患者一线 TKI 的使用模式,包括总体使用模式和特定药物的使用模式,以及成本影响。
从链接的监测、流行病学和最终结果(SEER)-医疗保险数据库中的基于人群的癌症登记处确定了 2007 年至 2015 年诊断时年龄在 65 岁及以上的 CML 患者。计算了诊断后第一年接受伊马替尼、达沙替尼或尼洛替尼的 CML 患者的百分比,以及一线治疗开始的时间。使用双变量比较和 Cox 比例风险模型来确定与 TKI 起始相关的因素。还计算了按患者的医疗保险部分 D(Part D)低收入补贴(LIS)状况分层的患者的平均每月患者责任,包括患者自付费用(OOP)。
在纳入的 1589 名 CML 患者中,在诊断后 1 年内接受任何 TKI 的患者比例从 66.2%增加到 78.9%。2015 年,一线 TKI 治疗的分布为 41.3%伊马替尼、28.3%达沙替尼和 9.3%尼洛替尼。近 60%的患者在诊断后 3 个月内开始 TKI 治疗。多变量分析表明,在非常高龄(>75 岁)的患者中,第一年 TKI 的使用率较低(与 65-69 岁相比:HR=0.72;95%CI=0.63-0.83),合并症较多的患者(分层健康状况类别风险评分>2 与 HR=0.74,95%CI=0.62-0.88),以及不符合 LIS 资格的患者(HR=0.75;95%CI=0.65-0.87)。符合 LIS 资格的患者与不符合 LIS 资格的患者相比,每月患者 OOP 费用显著降低:伊马替尼(2016 年:$12 比 $487)、达沙替尼(2016 年:$34 比 $557)和尼洛替尼(2016 年:$1 比 $526)。自 2007 年以来,TKI 的使用显著增加。虽然伊马替尼仍然是最常开的一线药物,但到 2015 年,新型 TKI 占市场份额的三分之一。使用模式表明,年龄、合并症和经济障碍仍然存在。TKI 适用于长期治疗,新型、更昂贵药物的广泛采用引起了人们对 CML 治疗可持续性的担忧,特别是在没有补贴的患者中。本研究没有外部资金支持。没有报道的利益冲突。