Institute for Health Economics and Clinical Epidemiology, The University Hospital of Cologne (AöR), Gleueler Straße 176-178, 50935, Cologne, Germany.
Center for Hereditary Breast and Ovarian Cancer, University Hospital Cologne, Kerpener Straße 34, 50931, Cologne, Germany.
Eur J Health Econ. 2019 Jul;20(5):739-750. doi: 10.1007/s10198-019-01038-1. Epub 2019 Feb 21.
The 'German Consortium for Hereditary Breast and Ovarian Cancer' (GC-HBOC) offers women with a family history of breast and ovarian cancer genetic counseling. The aim of this modeling study was to evaluate the cost-effectiveness of genetic testing for BRCA 1/2 in women with a high familial risk followed by different preventive interventions (intensified surveillance, risk-reducing bilateral mastectomy, risk-reducing bilateral salpingo-oophorectomy, or both mastectomy and salpingo-oophorectomy) compared to no genetic test.
A Markov model with a lifelong time horizon was developed for a cohort of 35-year-old women with a BRCA 1/2 mutation probability of ≥ 10%. The perspective of the German statutory health insurance (SHI) was adopted. The model included the health states 'well' (women with increased risk), 'breast cancer without metastases', 'breast cancer with metastases', 'ovarian cancer', 'death', and two post (non-metastatic) breast or ovarian cancer states. Outcomes were costs, quality of life years gained (QALYs) and life years gained (LYG). Important data used for the model were obtained from 4380 women enrolled in the GC-HBOC.
Compared with the no test strategy, genetic testing with subsequent surgical and non-surgical treatment options provided to women with deleterious BRCA 1 or 2 mutations resulted in additional costs of €7256 and additional QALYs of 0,43 (incremental cost-effectiveness ratio of €17,027 per QALY; cost per LYG: €22,318). The results were robust in deterministic and probabilistic sensitivity analyses.
The provision of genetic testing to high-risk women with a BRCA1 and two mutation probability of ≥ 10% based on the individual family cancer history appears to be a cost-effective option for the SHI.
德国遗传性乳腺癌和卵巢癌联盟(GC-HBOC)为有乳腺癌和卵巢癌家族史的女性提供遗传咨询。本建模研究旨在评估对高风险家族史的女性进行 BRCA1/2 基因检测,并随后采取不同的预防干预措施(强化监测、预防性双侧乳房切除术、预防性双侧输卵管卵巢切除术,或双侧乳房切除术和输卵管卵巢切除术)与不进行基因检测相比的成本效益。
为 BRCA1/2 突变概率≥10%的 35 岁女性队列开发了一个具有终身时间范围的 Markov 模型。采用德国法定健康保险(SHI)的观点。该模型包括“健康”(风险增加的女性)、“无转移乳腺癌”、“有转移乳腺癌”、“卵巢癌”、“死亡”和两个(非转移性)乳腺癌或卵巢癌后状态。结果是成本、获得的质量调整生命年(QALYs)和获得的生命年(LYG)。模型中使用的重要数据来自参加 GC-HBOC 的 4380 名女性。
与不检测策略相比,对携带有害 BRCA1 或 2 突变的女性进行基因检测,并随后提供手术和非手术治疗选择,导致额外的 7256 欧元成本和 0.43 个 QALY(增量成本效益比为每 QALY 17027 欧元;每 LYG 的成本为 22318 欧元)。确定性和概率敏感性分析的结果是稳健的。
根据个体家族癌症史,对 BRCA1 和 2 突变概率≥10%的高风险女性提供基因检测,对 SHI 来说似乎是一种具有成本效益的选择。