Department of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, AL, USA.
Division of Gynecologic Oncology, University of Alabama at Birmingham, Birmingham, AL, USA.
Gynecol Oncol. 2015 Oct;139(1):59-62. doi: 10.1016/j.ygyno.2015.08.013. Epub 2015 Aug 22.
To determine the cost-effectiveness of olaparib, a PARP inhibitor, as maintenance therapy for platinum-sensitive (PS) recurrent ovarian cancer.
Two separate decision analysis models compared the cost of observation versus olaparib maintenance therapy in patients with PS recurrent ovarian cancer, one for patients with a germline BRCA1/2 mutation and one for patients with wild-type BRCA1/2. Patients received six cycles of paclitaxel and carboplatin. Drug costs were estimated using 2014-2015 wholesale acquisition costs. The cost of olaparib was estimated at $13,440 per month. Rate of germline BRCA1/2 mutation was estimated at 20%. Progression-free survival was determined from published data. Incremental cost-effectiveness ratios (ICERs) per progression-free life-year saved (PF-LYS) were calculated. A sensitivity analysis estimated the cost at which olaparib would be cost-effective.
We estimated that there were 5549 patients diagnosed with PS recurrent ovarian cancer in the United States annually. The cost of observation in 1110 patients with a BRCA1/2 mutation was $5.5 million (M) versus $169.2M for maintenance therapy with olaparib. The ICER for olaparib maintenance therapy in patients with a BRCA mutation was $258,864 per PF-LYS. If the cost of olaparib was decreased to $2500 per month, the ICER was $49,584. For the 4439 patients with wild-type BRCA, the cost of maintenance therapy was $444.2M; the ICER was $600,552 per PF-LYS.
For patients with a germline BRCA1/2 mutation, maintenance therapy with olaparib is not cost-effective with an ICER of $258,864 per PF-LYS. To achieve an ICER of less than $50,000, the cost of olaparib should be $2500 or less per month. For wild-type BRCA1/2 patients, maintenance therapy with olaparib is not cost-effective.
确定聚腺苷二磷酸核糖聚合酶(PARP)抑制剂奥拉帕利作为铂类敏感(PS)复发性卵巢癌维持治疗的成本效益。
两个独立的决策分析模型比较了 PS 复发性卵巢癌患者观察与奥拉帕利维持治疗的成本,一个针对胚系 BRCA1/2 突变患者,另一个针对野生型 BRCA1/2 患者。患者接受六周期紫杉醇和卡铂治疗。药物成本使用 2014-2015 年批发采购成本进行估算。奥拉帕利的成本估计为每月 13440 美元。胚系 BRCA1/2 突变率估计为 20%。无进展生存期(PFS)从已发表的数据中确定。计算每获得一个无进展生存生命年(PF-LYS)的增量成本效益比(ICER)。敏感性分析估计了奥拉帕利具有成本效益的成本。
我们估计,美国每年有 5549 例 PS 复发性卵巢癌患者。1110 例 BRCA1/2 突变患者的观察成本为 5500 万美元(M),而奥拉帕利维持治疗的成本为 16920 万美元。BRCA 突变患者奥拉帕利维持治疗的 ICER 为每 PF-LYS 258864 美元。如果奥拉帕利的成本降低到每月 2500 美元,ICER 为 49584 美元。对于 4439 例野生型 BRCA 患者,维持治疗的成本为 44420 万美元;ICER 为每 PF-LYS 600552 美元。
对于存在胚系 BRCA1/2 突变的患者,奥拉帕利维持治疗的 ICER 为每 PF-LYS 258864 美元,不具有成本效益。要达到低于 50000 美元的 ICER,奥拉帕利的成本应低于每月 2500 美元。对于野生型 BRCA1/2 患者,奥拉帕利维持治疗不具有成本效益。