AstraZeneca Nordic-Baltic, Södertälje, Sweden.
Department of Medical Sciences, Respiratory, Allergy and Sleep Research, Uppsala University, Uppsala, Sweden.
J Med Econ. 2020 Aug;23(8):877-884. doi: 10.1080/13696998.2020.1760285. Epub 2020 May 13.
We investigated cost effectiveness of benralizumab vs. standard of care (SOC) plus oral corticosteroids (OCS) for patients with severe, eosinophilic OCS-dependent asthma in Sweden. A three-state, cohort-based Markov model of data from three Phase III benralizumab clinical trials (ZONDA [NCT02075255], SIROCCO [NCT01928771], and CALIMA [NCT01914757]) was used to assess the incremental cost-effectiveness ratio of benralizumab vs. SOC plus OCS. Health outcomes were estimated in terms of quality-adjusted life-years (QALYs). The model included costs and disutilities associated with extrapolated OCS-related adverse events. Patients with severe asthma were defined as those receiving OCS ≥5 mg/day. Benralizumab demonstrated a cost-effectiveness ratio vs. SOC plus OCS of 2018 Swedish Kronor (SEK) 366,855 (€34,127) per QALY gained, based on increases of 1.33 QALYs and SEK 488,742 (€45,344) per patient. Benralizumab treatment costs contributed most to incremental costs. The probability of benralizumab's being cost-effective with willingness-to-pay (WTP) thresholds between SEK 429,972 (€40,000) and SEK 752,452 (€70,000) ranged from 75% to 99%. Potential limitations of these analyses include the use of combined data from three different clinical trials, a one-way sensitivity analysis that did not include mortality and transition estimates, and Observational & Pragmatic Research Institute (OPRI) data from the UK as a proxy of the Swedish health care system. The results of these analyses demonstrate that benralizumab has a high probability of being cost-effective compared with SOC plus OCS for a subgroup of patients with severe, eosinophilic asthma receiving regular OCS treatment and may support clinicians, payers and patients in making treatment decisions.
我们研究了贝那鲁肽对比标准治疗(SOC)加口服皮质类固醇(OCS)在瑞典重度嗜酸性粒细胞性 OCS 依赖型哮喘患者中的成本效果。采用来自三项贝那鲁肽 III 期临床试验(ZONDA [NCT02075255]、SIROCCO [NCT01928771]和 CALIMA [NCT01914757])数据的三状态、队列基础马尔可夫模型来评估贝那鲁肽对比 SOC 加 OCS 的增量成本效果比。健康结果以质量调整生命年(QALY)来评估。模型纳入了因 OCS 相关不良事件外推所致的成本和非效用值。重度哮喘患者定义为每日接受 OCS≥5mg 的患者。贝那鲁肽对比 SOC 加 OCS 的成本效果比为每增加 1.33QALY 和每位患者增加 SEK 488,742(€45,344),瑞典克朗(SEK)366,855(€34,127)。贝那鲁肽治疗成本对增量成本的贡献最大。贝那鲁肽的成本效果比在 SEK 429,972(€40,000)至 SEK 752,452(€70,000)之间的意愿支付(WTP)阈值范围内的概率为 75%至 99%。这些分析的潜在局限性包括使用来自三项不同临床试验的合并数据、不包括死亡率和过渡估计的单向敏感性分析,以及英国观察性和实用研究学会(OPRI)数据作为瑞典医疗保健系统的替代。这些分析的结果表明,贝那鲁肽在重度嗜酸性粒细胞性哮喘患者中与 SOC 加 OCS 相比,具有较高的成本效果概率,这些患者需要定期接受 OCS 治疗,这可能有助于临床医生、支付方和患者做出治疗决策。