Is Alpelisib Plus Fulvestrant Cost-Effective for Treating PIK3CA-Mutation, HR+/HER2- Advanced Breast Cancer in the USA?

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY Clinical Drug Investigation Pub Date : 2023-12-01 Epub Date: 2023-11-17 DOI:10.1007/s40261-023-01325-z
Wenhua Wu, Huiting Lin, Jiaqin Cai, Hong Sun, Jia Liu, Congting Hu, Xiaoxia Wei
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Abstract

Background and objective: There is a considerable survival benefit of alpelisib in patients with PIK3CA-mutated, hormone receptor-positive and human epidermal growth factor receptor 2-negative advanced breast cancer (HR+/HER2- ABC), yet the financial burden may limit its use. Therefore, this study evaluated the cost-effectiveness of alpelisib plus fulvestrant in patients with PIK3CA-mutated, HR+/HER2- ABC in the USA.

Methods: A Markov model was constructed to simulate the progression of PIK3CA-mutated, HR+/HER2- ABC. Efficacy and safety data were derived from the SOLAR-1 trial. A parametric survival model was used to explore the long-term effect. From a US payer perspective, only direct medical costs were considered. The cost data were estimated based on local pricing and relevant literature. The health outcomes were expressed in quality-adjusted life years (QALYs). Model stability was assessed using one-way sensitivity analysis and probability sensitivity analysis. Subgroup analyses were performed to explore cost-effectiveness outcomes for patients with different clinical characteristics.

Results: The QALY increased by 0.28 with alpelisib plus fulvestrant with an additional cost of $94,345.87 compared with placebo plus fulvestrant, leading to an incremental cost-effectiveness ratio (ICER) of $340,153.30/QALY gained. Sensitivity analyses suggested that the model is most sensitive to the price of alpelisib. At a willingness-to-pay (WTP) threshold of $150,000/QALY, alpelisib plus fulvestrant was cost effective when the cost of alpelisib was less than $71 per 300 mg (36.5 % of the original price), whereas this cost would be less than $168 per 300 mg (86.5 % of the original price) at a WTP threshold of $300,000/QALY. In addition, alpelisib + fulvestrant was not cost effective in all subgroups compared with placebo + fulvestrant at the WTP threshold of $150,000/QALY. In contrast, at the WTP threshold of $300,000/QALY, alpelisib + fulvestrant was cost effective in nearly all subgroups except for endocrine-sensitive patients.

Conclusion: At current drug prices, alpelisib plus fulvestrant is not cost effective for patients with PIK3CA-mutated, HR+/HER2- ABC from a US payer perspective. Given the considerable progression-free survival (PFS) and overall survival (OS) benefits observed with alpelisib in this setting, further discussion and negotiation of the price of alpelisib are warranted to provide more favorable economic outcomes and thereby increase the value of the alpelisib plus fulvestrant regimen in patients.

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在美国,Alpelisib + Fulvestrant治疗pik3ca突变、HR+/HER2-晚期乳腺癌是否具有成本效益?
背景与目的:在pik3ca突变、激素受体阳性和人表皮生长因子受体2阴性的晚期乳腺癌(HR+/HER2- ABC)患者中,alpelisib有相当大的生存获益,但经济负担可能限制了其使用。因此,本研究在美国评估了alpelisib加氟维司汀治疗pik3ca突变的HR+/HER2- ABC患者的成本-效果。方法:建立Markov模型,模拟pik3ca突变的HR+/HER2- ABC的进展。疗效和安全性数据来自SOLAR-1试验。采用参数生存模型探讨长期效果。从美国付款人的角度来看,只考虑直接医疗费用。成本数据是根据当地定价和相关文献估算的。健康结果以质量调整生命年(QALYs)表示。采用单向敏感性分析和概率敏感性分析对模型稳定性进行评价。进行亚组分析以探讨不同临床特征患者的成本-效果结果。结果:与安慰剂加氟维司汀相比,alpelisib加氟维司汀的QALY增加了0.28,额外的成本为94,345.87美元,导致增量成本-效果比(ICER)为340,153.30美元/QALY获得。敏感性分析表明,该模型对紫苏的价格最为敏感。在支付意愿(WTP)阈值为150,000美元/QALY时,当alpelisib的成本低于每300毫克71美元(原价的36.5%)时,alpelisib加氟维司汀具有成本效益,而在WTP阈值为300,000美元/QALY时,该成本将低于每300毫克168美元(原价的86.5%)。此外,在WTP阈值为15万美元/QALY时,与安慰剂+氟维司汀相比,alpelisib +氟维司汀并非在所有亚组中都具有成本效益。相比之下,在300,000美元/QALY的WTP阈值下,alpelisib + fulvestrant在除内分泌敏感患者外的几乎所有亚组中都具有成本效益。结论:从美国付款人的角度来看,以目前的药物价格,alpelisib加氟维司汀对pik3ca突变的HR+/HER2- ABC患者没有成本效益。鉴于alpelisib在这种情况下观察到的可观的无进展生存期(PFS)和总生存期(OS)益处,有必要对alpelisib的价格进行进一步讨论和谈判,以提供更有利的经济结果,从而提高alpelisib +氟维司汀方案对患者的价值。
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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional 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 Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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