Ward Melea A, Fang Gang, Richards Kristy L, Walko Christine M, Earnshaw Stephanie R, Happe Laura E, Blalock Susan J
University of North Carolina, Department of Pharmaceutical Outcomes and Policy , Chapel Hill, NC , USA.
Curr Med Res Opin. 2015 Feb;31(2):289-97. doi: 10.1185/03007995.2014.991440. Epub 2014 Dec 10.
Chronic myeloid leukemia (CML) treatment guidelines recommend first-line therapy with either first- or second-generation tyrosine kinase inhibitors (1GTKI, 2GTKI), but do not specify which generation should be used first.
To examine the association between initiation of 2GTKI versus 1GTKI and medication adherence, health services utilization, and healthcare costs.
This was a retrospective cohort study utilizing administrative claims data from a single health plan within the US of commercial and Medicare patients newly initiating 1GTKI or 2GTKI therapy for CML between June 2010 and December 2011. Multivariate logistic regression was used to investigate the association between TKI therapy and adherence, defined as proportion of days covered ≥0.85. Multivariate logistic regression and generalized linear models examined the association between TKI and health services utilization and direct healthcare costs (plan and patient paid) during the 12 month follow-up period.
Among the 368 patients included, there was no difference in adherence between patients initiating a 2GTKI compared to a 1GTKI (odds ratio = 0.88, 95% confidence interval [CI] 0.55-1.40). Initiating a 2GTKI was associated with increased outpatient visits (incidence rate ratio [IRR] = 1.12, 95% CI 1.06-1.20); however, there were no statistically significant differences in emergency room visits or inpatient visits between the treatment groups. Total costs were 1.3 times higher for 2GTKI initiators versus 1GTKI initiators ($86,509 versus $66,443; p = 0.001), with a significant difference in TKI pharmacy costs.
Although there were no differences in adherence, hospitalizations, or emergency room visits among patients initiating a second- versus first-generation TKI, total all-cause costs and outpatient visits were higher for 2GTKI initiators. With the impending release of generic imatinib, these comparative data will become germane in the selection of a first-line TKI therapy. Because this study used claims from a single health plan, it may not be generalizable to the general population.
慢性粒细胞白血病(CML)治疗指南推荐使用第一代或第二代酪氨酸激酶抑制剂(1GTKI、2GTKI)进行一线治疗,但未明确应首先使用哪一代。
研究开始使用2GTKI与1GTKI治疗与药物依从性、医疗服务利用及医疗费用之间的关联。
这是一项回顾性队列研究,利用美国一家单一医保计划中2010年6月至2011年12月期间新开始使用1GTKI或2GTKI治疗CML的商业保险和医疗保险患者的管理索赔数据。采用多因素逻辑回归分析来研究酪氨酸激酶抑制剂(TKI)治疗与依从性之间的关联,依从性定义为覆盖天数比例≥0.85。多因素逻辑回归和广义线性模型用于研究TKI与12个月随访期内医疗服务利用及直接医疗费用(医保和患者支付)之间的关联。
在纳入的368例患者中,开始使用2GTKI的患者与开始使用1GTKI的患者在依从性方面无差异(优势比=0.88,95%置信区间[CI]为0.55 - 1.40)。开始使用2GTKI与门诊就诊次数增加相关(发病率比[IRR]=1.12,95%CI为1.06 - 1.20);然而,治疗组之间在急诊就诊或住院就诊方面无统计学显著差异。2GTKI起始者的总费用比1GTKI起始者高1.3倍(86,509美元对66,443美元;p = 0.001),TKI药房费用存在显著差异。
尽管开始使用第二代与第一代TKI的患者在依从性、住院或急诊就诊方面无差异,但2GTKI起始者的全因总费用和门诊就诊次数更高。随着通用型伊马替尼即将上市,这些比较数据在一线TKI治疗的选择中将变得至关重要。由于本研究使用的是单一医保计划的索赔数据,可能不适用于一般人群。