Stacie B. Dusetzina, School of Medicine and Lineberger Comprehensive Cancer Center and Cecil G. Sheps Center for Health Services Research; Stacie B. Dusetzina and Aaron N. Winn, Gillings School of Global Public Health; University of North Carolina at Chapel Hill, Chapel Hill, NC; Gregory A. Abel, Dana-Farber Cancer Institute; Haiden A. Huskamp and Nancy L. Keating, Harvard Medical School; and Nancy L. Keating, Brigham and Women's Hospital, Boston, MA.
J Clin Oncol. 2014 Feb 1;32(4):306-11. doi: 10.1200/JCO.2013.52.9123. Epub 2013 Dec 23.
The introduction of imatinib, a tyrosine kinase inhibitor (TKI), has greatly increased survival for patients with chronic myeloid leukemia (CML). Conversely, nonadherence to imatinib and other TKIs undoubtedly results in disease progression and treatment resistance. We examined trends in imatinib expenditures from 2002 to 2011 and assessed the association between copayment requirements for imatinib and TKI adherence.
We used MarketScan health plan claims from 2002 to 2011 to identify adults (age 18 to 64 years) with CML who initiated imatinib therapy between January 1, 2002, and June 30, 2011, and had insurance coverage for at least 3 months before through 6 months after initiation (N = 1,541). Primary outcomes were TKI discontinuation and nonadherence. The primary independent variable was out-of-pocket cost for a 30-day supply of imatinib. By using a propensity-score weighted sample, we estimated the risk of discontinuation and nonadherence for patients with higher (top quartile) versus lower copayments.
Monthly copayments for imatinib averaged $108; median copayments were $30 (range, $0 to $4,792). Mean total monthly expenditures for imatinib nearly doubled between 2002 and 2011, from $2,798 to $4,892. Approximately 17% of patients with higher copayments and 10% with lower copayments discontinued TKIs during the first 180 days following initiation (adjusted risk ratio [aRR], 1.70; 95% CI, 1.30 to 2.22). Similarly, patients with higher copayments were 42% more likely to be nonadherent (aRR, 1.42; 95% CI, 1.19 to 1.69).
Patients with higher copayments are more likely to discontinue or be nonadherent to TKIs. Given the importance of these therapies for patients with CML, our data suggest a critical need to reduce patient costs for these therapies.
伊马替尼(一种酪氨酸激酶抑制剂[TKI])的问世极大地提高了慢性髓性白血病(CML)患者的生存率。相反,不遵守伊马替尼和其他 TKI 的用药规定无疑会导致疾病进展和治疗耐药。我们调查了 2002 年至 2011 年伊马替尼支出的趋势,并评估了伊马替尼共付要求与 TKI 依从性之间的关联。
我们使用 MarketScan 健康计划从 2002 年至 2011 年的索赔数据,确定了 2002 年 1 月 1 日至 2011 年 6 月 30 日期间开始接受伊马替尼治疗的年龄在 18 至 64 岁之间的 CML 成年患者(N=1541),并且在开始治疗前至少 3 个月至治疗后 6 个月内有保险。主要结局为 TKI 停药和不依从。主要的独立变量是 30 天伊马替尼供应的自付费用。通过使用倾向评分加权样本,我们估计了较高(最高四分位数)与较低共付额的患者停药和不依从的风险。
伊马替尼的月均自付费用平均为 108 美元;中位数自付额为 30 美元(范围:0 美元至 4792 美元)。2002 年至 2011 年间,伊马替尼的月平均总支出几乎翻了一番,从 2798 美元增加到 4892 美元。在开始治疗后的 180 天内,约有 17%的高自付费用患者和 10%的低自付费用患者停止使用 TKI(调整风险比[aRR],1.70;95%CI,1.30 至 2.22)。同样,高自付费用患者不依从的可能性增加了 42%(aRR,1.42;95%CI,1.19 至 1.69)。
自付费用较高的患者更有可能停止或不遵守 TKI 治疗规定。鉴于这些疗法对 CML 患者的重要性,我们的数据表明,迫切需要降低这些疗法的患者费用。