Boehringer Ingelheim International GmbH, Ingelheim, Germany.
Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, CT, USA.
J Med Econ. 2020 Jan;23(1):48-53. doi: 10.1080/13696998.2019.1645681. Epub 2019 Aug 9.
To assess healthcare resource utilization (HCRU) and costs in patients with non-small cell lung cancer treated with the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors afatinib or erlotinib as first-line treatment. This retrospective analysis used data from three large administrative claims databases in the US: Truven MarketScan, IMS PharMetrics Plus, and Optum Clinformatics Data Mart. Patients with diagnosis codes of lung cancer treated with afatinib or erlotinib were included in the sample. Treatment cohorts were matched on baseline characteristics using propensity scores to account for potential selection bias. HCRU and healthcare costs were compared between the matched afatinib and erlotinib cohorts. In total, 3,152 patients met the study inclusion criteria; propensity score matching of the afatinib and erlotinib patients yielded 525 matched pairs with well-balanced baseline characteristics. The afatinib cohort had significantly fewer patients with ≥1 inpatient visits (40.4% vs 52.2%, = 0.0001) and outpatient emergency room (ER) visits (45.7% vs 54.1%, = 0.0066). Per patient per month (PPPM) visits were significantly different between afatinib compared to erlotinib for inpatient visits (0.1 vs 0.2, = 0.0152), other outpatient visits PPPM (2.6 vs 3.0, = 0.022) and outpatient office visits (2.0 vs 1.7, = 0.0059). Although costs of outpatient office ($1,624 vs $1,070; = 0.0086) and pharmacy ($6,709 vs $5,932; < 0.0001) visits were higher for afatinib vs erlotinib, total costs did not differ significantly between cohorts ($14,972 vs $14,412; = 0.4415). Retrospective claims data can be subject to coding errors or data omissions; patients were required to have continuous health plan enrolment; EGFR mutation status was not confirmed. Patients treated with afatinib as first-line monotherapy experienced fewer inpatient stays and ER visits compared with erlotinib. Total costs were not significantly different between the two treatment cohorts.
评估表皮生长因子受体(EGFR)酪氨酸激酶抑制剂阿法替尼或厄洛替尼作为一线治疗非小细胞肺癌患者的医疗资源利用(HCRU)和成本。这项回顾性分析使用了来自美国三个大型行政索赔数据库的 Truven MarketScan、IMS PharMetrics Plus 和 Optum Clinformatics Data Mart 的数据。将诊断为肺癌并接受阿法替尼或厄洛替尼治疗的患者纳入样本。使用倾向评分对基线特征进行匹配,以考虑潜在的选择偏倚。比较匹配后的阿法替尼和厄洛替尼队列之间的 HCRU 和医疗保健成本。共有 3152 名患者符合研究纳入标准;对阿法替尼和厄洛替尼患者进行倾向评分匹配,生成了 525 对基线特征均衡的匹配对。阿法替尼组有明显更少的患者有≥1 次住院就诊(40.4% vs 52.2%,=0.0001)和门诊急诊就诊(45.7% vs 54.1%,=0.0066)。与厄洛替尼相比,阿法替尼患者的每患者每月就诊次数(PPPM)在住院就诊(0.1 次对 0.2 次,=0.0152)、其他门诊就诊(2.6 次对 3.0 次,=0.022)和门诊就诊(2.0 次对 1.7 次,=0.0059)方面存在显著差异。尽管阿法替尼的门诊就诊(1624 美元对 1070 美元;=0.0086)和药房就诊(6709 美元对 5932 美元;<0.0001)费用高于厄洛替尼,但两组的总费用无显著差异(14972 美元对 14412 美元;=0.4415)。回顾性索赔数据可能存在编码错误或数据遗漏;患者需要连续参加健康计划;未确认 EGFR 突变状态。与厄洛替尼相比,接受阿法替尼一线单药治疗的患者住院和急诊就诊次数较少。两个治疗组的总费用无显著差异。