Anderson Kristin R, Chambers Carole R, Lam Nadine, Yau Patrick S, Cusano Frances, Savoie M Lynn, Sheikh Naureen
Department of Pharmacy, Foothills Medical Centre, Calgary, Canada
Pharmacy Department, Tom Baker Cancer Centre, Calgary, Canada.
J Oncol Pharm Pract. 2015 Feb;21(1):19-25. doi: 10.1177/1078155213520261. Epub 2014 Feb 6.
Oral tyrosine kinase inhibitors are the standard of care for chronic myeloid leukemia. Tyrosine kinase inhibitors are administered in an outpatient setting for an indefinite period which may negatively impact adherence. Non-adherence to tyrosine kinase inhibitors is associated with disease progression.
To evaluate the need for adherence-enhancing interventions, this study was designed to determine the proportion of chronic myeloid leukemia patients non-adherent to their tyrosine kinase inhibitor regimen. The secondary objective was to identify the influence of patient characteristics on tyrosine kinase inhibitor adherence.
Cross-sectional retrospective chart and dispensing record reviews were performed to identify patients receiving a tyrosine kinase inhibitor from 1 June 2010 to 31 January 2012. Adherence was evaluated using the medication possession ratio.
A total of 124 patients were included. Thirty-eight (31%) patients were non-adherent to their tyrosine kinase inhibitor regimen. Patients not receiving concurrent medications were more likely to be non-adherent (odds ratio (OR) 2.33, 95% confidence interval (CI) 1.05-5.13, p=0.04). The median medication possession ratio was 0.95 (IQR=0.83-1.07). Median medication possession ratio was lower in patients receiving imatinib compared to dasatinib or nilotinib (0.95 vs. 1.00, p=0.01) and in those less than 50 years old compared to those greater than 50 years old (0.92 vs. 0.97, p=0.02).
Optimal tyrosine kinase inhibitor adherence in chronic myeloid leukemia patients poses a significant obstacle in achieving best possible outcomes while reducing healthcare costs. In this study, one in three chronic myeloid leukemia patients treated with a tyrosine kinase inhibitor were non-adherent to their regimen. Those at higher risk of non-adherence were on no concurrent medications, less than 50 years old, and those treated with imatinib. Active intervention to improve tyrosine kinase inhibitor adherence should be developed, implemented, and evaluated to improve patient outcomes at our center.
口服酪氨酸激酶抑制剂是慢性髓性白血病的标准治疗方法。酪氨酸激酶抑制剂需在门诊长期服用,这可能对依从性产生负面影响。不坚持服用酪氨酸激酶抑制剂与疾病进展相关。
为评估增强依从性干预措施的必要性,本研究旨在确定慢性髓性白血病患者中不坚持服用酪氨酸激酶抑制剂治疗方案的比例。次要目的是确定患者特征对酪氨酸激酶抑制剂依从性的影响。
进行横断面回顾性病历和配药记录审查,以确定2010年6月1日至2012年1月31日期间接受酪氨酸激酶抑制剂治疗的患者。使用药物持有率评估依从性。
共纳入124例患者。38例(31%)患者未坚持服用酪氨酸激酶抑制剂治疗方案。未同时服用其他药物的患者更有可能不依从(比值比(OR)2.33,95%置信区间(CI)1.05 - 5.13,p = 0.04)。药物持有率中位数为0.95(四分位间距=0.83 - 1.07)。与接受达沙替尼或尼罗替尼治疗的患者相比,接受伊马替尼治疗的患者药物持有率中位数较低(0.95对1.00,p = 0.01);与年龄大于50岁的患者相比,年龄小于50岁的患者药物持有率中位数较低(0.92对0.97,p = 0.02)。
慢性髓性白血病患者最佳的酪氨酸激酶抑制剂依从性是实现最佳治疗效果同时降低医疗成本的重大障碍。在本研究中,接受酪氨酸激酶抑制剂治疗的慢性髓性白血病患者中有三分之一未坚持治疗方案。不依从风险较高的人群包括未同时服用其他药物的患者、年龄小于50岁的患者以及接受伊马替尼治疗的患者。应制定、实施并评估积极干预措施以提高酪氨酸激酶抑制剂的依从性,从而改善我们中心患者的治疗效果。