Cost-Effectiveness Analysis of Ribociclib plus an Aromatase Inhibitor (AI) Versus AI Alone in the Adjuvant Treatment of Stage II and III Pre- and Postmenopausal Women with HR+/HER2- Early Breast Cancer (EBC): A Canadian Payer Perspective.

IF 2.4 Q2 ECONOMICS
Dina Soliman, Christine Brezden-Masley, Sandeep Sehdev, Khalid El Ouagari, Natalia Sabater Anaya, Daniel Stellato, Talitha Vincken
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引用次数: 0

Abstract

Background: Cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors have transformed the treatment of hormone receptor-positive (HR+) human epidermal growth factor receptor 2-negative (HER2-) breast cancer. Ribociclib plus an aromatase inhibitor (AI) was approved in Canada as adjuvant treatment for high-risk stage II-III early breast cancer (EBC) based on the phase 3 NATALEE trial, demonstrating improved invasive disease-free survival (iDFS) versus AI treatment alone. This study evaluated the cost-effectiveness of ribociclib plus AI versus AI alone and tamoxifen from a Canadian public payer perspective.

Methods: A non-homogeneous, semi-Markov cohort model with six health states (iDFS, second primary malignancy, non-metastatic recurrence, remission, distant recurrence [DR], and death) was developed, using Ontario-based costs (Canadian dollars) and a lifetime horizon. Transition probabilities from iDFS were derived from NATALEE trial data; other transitions were informed by published sources. DR was stratified by endocrine therapy (ET) sensitivity based on recurrence timing (≤ 12 months post-ET: resistant; > 12 months: sensitive), with outcomes and costs informed by prior health technology assessment evidence in metastatic disease. Results were reported as incremental cost-effectiveness ratios (ICERs) per quality-adjusted life-year (QALY) gained.

Results: Ribociclib plus AI yielded a probabilistic ICER of $45,097/QALY versus AI alone; tamoxifen was dominated by AI alone. Sensitivity analyses showed results were most sensitive to iDFS hazard rates and ribociclib drug costs. In the probabilistic analysis, ribociclib was preferred in 58.5% of simulations at a $50,000 willingness-to-pay threshold.

Conclusion: Ribociclib plus AI is cost-effective for HR+/HER2- EBC with an ICER of $45,097, below the $50,000 willingness-to-pay threshold versus AI or tamoxifen alone.

Ribociclib联合芳香酶抑制剂(AI)与单独使用AI辅助治疗II期和III期绝经前和绝经后HR+/HER2-早期乳腺癌(EBC)的成本-效果分析:加拿大支付款人的观点
背景:细胞周期蛋白依赖性激酶4和6 (CDK4/6)抑制剂已经改变了激素受体阳性(HR+)人表皮生长因子受体2阴性(HER2-)乳腺癌的治疗。Ribociclib +一种芳香酶抑制剂(AI)在加拿大被批准作为高风险II-III期早期乳腺癌(EBC)的辅助治疗,基于3期NATALEE试验,显示与单独使用AI相比,浸润性无病生存期(iDFS)得到改善。本研究从加拿大公共付款人的角度评估了核素西布加人工智能与单独使用人工智能和他莫西芬的成本效益。方法:采用基于安大略省的成本(加元)和生命周期,建立了一个具有六种健康状态(iDFS、第二原发恶性肿瘤、非转移性复发、缓解、远处复发[DR]和死亡)的非均匀半马尔可夫队列模型。iDFS的过渡概率来自NATALEE试验数据;其他的转变是由公开的消息来源提供的。根据复发时间(ET后≤12个月:耐药;12个月:敏感)的内分泌治疗(ET)敏感性对DR进行分层,转移性疾病的预后和成本由先前的卫生技术评估证据提供。结果报告为每个质量调整生命年(QALY)获得的增量成本-效果比(ICERs)。结果:与单独使用AI相比,Ribociclib加AI的概率ICER为45,097美元/QALY;他莫昔芬仅以AI为主。敏感性分析显示,结果对iDFS危险率和核糖素药物成本最为敏感。在概率分析中,在50,000美元的支付意愿阈值下,58.5%的模拟中首选ribociclib。结论:Ribociclib联合AI治疗HR+/HER2- EBC具有成本效益,ICER为45,097美元,低于50,000美元的支付意愿阈值,与单独使用AI或他莫昔芬相比。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
64
审稿时长
8 weeks
期刊介绍: PharmacoEconomics - Open focuses on applied research on the economic implications and health outcomes associated with drugs, devices and other healthcare interventions. The journal includes, but is not limited to, the following research areas:Economic analysis of healthcare interventionsHealth outcomes researchCost-of-illness studiesQuality-of-life studiesAdditional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in PharmacoEconomics -Open may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.All manuscripts are subject to peer review by international experts. Letters to the Editor are welcomed and will be considered for publication.
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