Cost-effectiveness of olaparib as a maintenance treatment for women with newly diagnosed advanced ovarian cancer and BRCA1/2 mutations in the United States

被引:15
|
作者
Muston, Dominic [1 ]
Hettle, Robert [2 ]
Monberg, Matthew [1 ]
McLaurin, Kimmie K. [3 ]
Gao, Wei [4 ]
Swallow, Elyse [4 ]
Zhang, Su [4 ]
Kalemaj, Iden [4 ]
Signorovitch, James [4 ]
Moore, Kathleen [5 ]
机构
[1] Merck & Co Inc, 2000 Galloping Hill Rd, Kenilworth, NJ 07033 USA
[2] AstraZeneca, Acad House,136 Hills Rd, Cambridge, England
[3] AstraZeneca, One MedImmune Way, Gaithersburg, MD 20878 USA
[4] Anal Grp Inc, 111 Huntington Ave,14th Floor, Boston, MA 02199 USA
[5] Univ Oklahoma, Oklahoma City, OK USA
关键词
Ovarian cancer; Cost-effectiveness; Maintenance treatment; Olaparib; HOMOLOGOUS RECOMBINATION GENES; DOUBLE-BLIND; BEVACIZUMAB; SURVIVAL; THERAPY;
D O I
10.1016/j.ygyno.2020.08.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. This study evaluated the cost-effectiveness of olaparib monotherapy in the first-line maintenance setting vs. surveillance in women with newly diagnosed advanced ovarian cancer and a BRCA1/2 mutation from a US third-party payer perspective. Methods. A three-state (progression free, progressed disease, and death) partitioned survival model over a 50-year lifetime horizon was developed. Piecewise models were applied to data from the phase III trial SOLO1 to extrapolate survival outcomes. Health state utilities and adverse event disutilities were obtained from literature and SOLO1. Treatment costs, adverse event costs, and medical costs associated with health states were obtained from publicly available databases, SOLO1, and real-world data. Time on treatment was estimated using the data from SOLO1. Incremental costs per quality-adjusted life year (QALY) and life year (LY) gained were estimated. One-way deterministic and probabilistic sensitivity analyses were conducted. Results. Over a lifetime horizon, olaparib was associated with an additional 3.63 LYs and 2.93 QALYs, and an incremental total cost of $152,545 vs. surveillance. Incremental cost per LY gained and per QALY gained for olaparib were $42,032 and $51,986, respectively. The incremental cost-effectiveness ratios remained below $100,000 across a range of inputs and scenarios. In the PSA, the probability of olaparib being cost-effective at a $100,000 per QALY threshold was 99%. Conclusions. Compared to surveillance, olaparib increases both the LYs and QALYs of women with newly diagnosed advanced ovarian cancer and with a germline or somatic BRCA mutation. Olaparib offers a cost-effective maintenance option for these women from a US third-party payer perspective. (C) 2020 The Authors. Published by Elsevier Inc.
引用
收藏
页码:491 / 497
页数:7
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