Podkonjak Tanja, Cranmer Holly, Scarisbrick Julia, McCarthy Grant, Lilley Cameron, Cheng Lung-I
Takeda Pharmaceuticals International Co., London, UK.
Department of Dermatology, University Hospital Birmingham, Birmingham, B15 2TH, UK.
J Comp Eff Res. 2022 Feb;11(3):193-202. doi: 10.2217/cer-2021-0201. Epub 2021 Dec 9.
To assess the cost-effectiveness of brentuximab vedotin (BV) versus physician's choice (methotrexate or bexarotene) for treating advanced cutaneous T-cell lymphoma. A partitioned-survival model was developed from the National Health Service perspective in England and Wales. Model inputs were informed by the ALCANZA trial, real-world UK data, published literature or clinical experts. Over the modeled lifetime, BV dominated physician's choice and provided an additional 1.58 life-years and 1.09 higher quality-adjusted life years with a net cost saving of £119,565. The net monetary benefit was £152,326 using a willingness-to-pay threshold of £30,000/quality-adjusted life year. Results were robust in sensitivity and scenario analyses. BV is a highly cost-effective treatment for advanced cutaneous T-cell lymphoma.
评估用于治疗晚期皮肤T细胞淋巴瘤的本妥昔单抗(BV)相对于医生选择的药物(甲氨蝶呤或贝沙罗汀)的成本效益。从英国国家医疗服务体系的角度出发,在英格兰和威尔士建立了一个分段生存模型。模型输入数据来源于ALCANZA试验、英国真实世界数据、已发表文献或临床专家。在模拟的生存期内,BV相对于医生选择的药物具有优势,可额外增加1.58个生命年和1.09个质量调整生命年,净成本节省119,565英镑。使用30,000英镑/质量调整生命年的支付意愿阈值,净货币收益为152,326英镑。敏感性分析和情景分析的结果具有稳健性。BV是治疗晚期皮肤T细胞淋巴瘤的一种极具成本效益的治疗方法。