Chang Raymond C, Huang Joanna, Hurst James, Reck Daniel, Khachatourian Kat, Shannon Michael H
AstraZeneca Payer Evidence, US Medical, Wilmington, DE.
AstraZeneca, Cardiovascular Metabolic Disease, US Medical, Wilmington, DE.
J Manag Care Spec Pharm. 2024 Aug;30(8):834-842. doi: 10.18553/jmcp.2024.30.8.834.
One in 7 adults have chronic kidney disease (CKD), which is associated with high morbidity and mortality and substantial health care costs, especially in more advanced disease. Our data from a US commercial payer show rising per-member-per-year costs for renal and cardiac complications associated with CKD.
To predict the clinical and economic impact of treatment with or without dapagliflozin from the perspective of a US commercial payer using a cost-offset model (COM).
The COM used real-world cost and member count data from a US employer-sponsored commercial payer and results of the double-blind, randomized, phase 3 Dapagliflozin and Prevention of Adverse Outcomes in CKD clinical trial (NCT03036150) to predict the incidence of clinical events, including a greater than or equal to 50% decline in estimated glomerular filtration rate (eGFR), end-stage kidney disease, and hospitalization for heart failure, and their associated costs over a 3-year period. The COM compared a hypothetical scenario of the experience with or without dapagliflozin in members with CKD stages 2-4, aged younger than 65 years.
In the simulated populations of 130 members, the COM projected 9 events of a greater than or equal to 50% decline in estimated glomerular filtration rate for the experience with dapagliflozin vs 15 events for the experience without dapagliflozin (6 fewer events; number needed to treat [NNT] = 20, amounting to estimated cumulative cost offsets of $0.57 million [M] over a 3-year period). The COM projected similar results for end-stage kidney disease (8 events with dapagliflozin vs 14 events without dapagliflozin; NNT = 24, amounting to $1.92 M in cumulative cost offsets) and for hospitalization for heart failure (13 events with dapagliflozin vs 33 events without dapagliflozin; NNT = 7, amounting to $0.79 M in cumulative cost offsets). These projections translated to total mean, cumulative cost offsets of $3.89 M for all clinical events evaluated over the 3-year period (36.6% reduction with dapagliflozin vs without dapagliflozin), and net mean, cumulative cost offsets of $2.58 M over the 3-year period (24.2% reduction with dapagliflozin vs without dapagliflozin) after factoring in a discounted wholesale acquisition cost for dapagliflozin expenditure ($1.31 M over 3 years). Thus, the net mean, cumulative cost offsets were $19,843 per member over 3 years, representing a 197% return on investment for dapagliflozin expenditure.
Results of our COM suggest that dapagliflozin can reduce clinical events and their associated costs over a 3-year period when compared with a scenario without dapagliflozin. Cost offsets increased with each year, indicating that US commercial payers can substantially reduce costs associated with CKD morbidity and mortality.
七分之一的成年人患有慢性肾脏病(CKD),其与高发病率、高死亡率以及巨额医疗费用相关,尤其是在疾病进展到更严重阶段时。我们从美国一家商业医保机构获取的数据显示,与CKD相关的肾脏和心脏并发症的人均年度费用在不断上升。
从美国商业医保机构的角度,使用成本抵消模型(COM)预测达格列净治疗或不治疗的临床和经济影响。
COM使用了来自美国一个由雇主赞助的商业医保机构的真实世界成本和参保人数数据,以及双盲、随机、3期达格列净与CKD不良结局预防临床试验(NCT03036150)的结果,以预测临床事件的发生率,包括估计肾小球滤过率(eGFR)下降大于或等于50%、终末期肾病以及因心力衰竭住院,及其在3年期间的相关成本。COM比较了在年龄小于65岁的2 - 4期CKD患者中使用或不使用达格列净的假设情况。
在130名成员的模拟人群中,COM预测使用达格列净的情况下估计肾小球滤过率下降大于或等于50%的事件有9起,而不使用达格列净的情况下有15起(减少6起;治疗所需人数[NNT]=已翻译内容中未提及,原文为20,3年期间估计累计成本抵消为57万美元)。COM对终末期肾病(使用达格列净8起事件,不使用达格列净14起事件;NNT = 24,累计成本抵消为192万美元)和因心力衰竭住院(使用达格列净13起事件,不使用达格列净33起事件;NNT = 7,累计成本抵消为79万美元)的预测结果相似。这些预测转化为在3年期间对所有评估的临床事件的总平均累计成本抵消为389万美元(使用达格列净比不使用达格列净减少36.6%),在考虑到达格列净支出的折扣后批发采购成本(3年期间为131万美元)后,3年期间的净平均累计成本抵消为258万美元(使用达格列净比不使用达格列净减少24.2%)。因此,3年期间人均净平均累计成本抵消为19,843美元,代表达格列净支出的投资回报率为197%。
我们的COM结果表明,与不使用达格列净的情况相比,达格列净在3年期间可减少临床事件及其相关成本。成本抵消逐年增加,表明美国商业医保机构可大幅降低与CKD发病率和死亡率相关的成本。