Cost-Effectiveness Analysis of PI3K Inhibitors for Relapsed or Refractory Follicular Lymphoma in China: A Comparison Between Linperlisib and Duvelisib.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Clinical Drug Investigation Pub Date : 2026-05-01 Epub Date: 2026-03-10 DOI:10.1007/s40261-026-01532-4
Xuefei Bai, Rongjie Shao, Xiaoning He
{"title":"Cost-Effectiveness Analysis of PI3K Inhibitors for Relapsed or Refractory Follicular Lymphoma in China: A Comparison Between Linperlisib and Duvelisib.","authors":"Xuefei Bai, Rongjie Shao, Xiaoning He","doi":"10.1007/s40261-026-01532-4","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Linperlisib, a highly selective PI3K-δ inhibitor, was firstly approved in China in November 2022 for the treatment of patients with relapsed or refractory follicular lymphoma (r/r FL) who had received at least two prior lines of systemic therapy (3L+ FL), demonstrating compelling clinical efficacy.</p><p><strong>Objective: </strong>This study aimed to evaluate the cost effectiveness of linperlisib compared to duvelisib for patients with 3L+ FL from the perspective of Chinese healthcare system.</p><p><strong>Methods: </strong>A lifetime three-state partitioned survival model was developed to integrate comparative efficacy and direct costs. An unanchored matching-adjusted indirect comparison (MAIC) was conducted using individual data from NCT04370405 and published aggregate data from the DYNAMO trial, aiming to derive comparative efficacy data and calculate patients' life-years gained. Utility values were from GADOLIN study, as neither trial collected them. Quality-adjusted life-years (QALYs) were calculated by multiplying life-years by utility values. Direct costs included costs of drug acquisition, adverse events, subsequent salvage therapy, health-care resource use (HCRU), and end-of-life care. A 5% annual discount rate was applied to both future QALYs and costs. The primary outcome was the incremental cost-effectiveness ratio (ICER), calculated as discounted incremental costs divided by incremental QALYs. The willingness-to-pay (WTP) threshold was set at China's 2023 per capita GDP (CNY89,358/QALY), with an ICER below this threshold indicating linperlisib was more cost effective. Model robustness was verified via one-way deterministic and probabilistic sensitivity analyses (DSA and PSA).</p><p><strong>Results: </strong>In the base-case analysis, linperlisib yielded an additional 1.58 QALYs (4.13 vs 2.55) at an incremental cost of CNY108,780 (CNY292,805 vs CNY184,025) compared with duvelisib. The resulting ICER was CNY68,996 per QALY, which was below the WTP. Although drug costs were the main cost driver, improved survival reduced end-of-life care costs by CNY1,507. Deterministic sensitivity analysis identified the price of linperlisib as the top influential parameter, yet all ICERs stayed below the WTP threshold. Probabilistic sensitivity analysis showed a 91.2% cost-effectiveness probability at the preset WTP, confirming robust findings.</p><p><strong>Conclusions: </strong>Linperlisib is cost effective compared to duvelisib for 3L+ FL patients in China, as verified in sensitivity analyses. Further study is warranted to confirm that it meets an unmet need in China.</p>","PeriodicalId":10402,"journal":{"name":"Clinical Drug Investigation","volume":" ","pages":"571-581"},"PeriodicalIF":3.1000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Drug Investigation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s40261-026-01532-4","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/3/10 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Linperlisib, a highly selective PI3K-δ inhibitor, was firstly approved in China in November 2022 for the treatment of patients with relapsed or refractory follicular lymphoma (r/r FL) who had received at least two prior lines of systemic therapy (3L+ FL), demonstrating compelling clinical efficacy.

Objective: This study aimed to evaluate the cost effectiveness of linperlisib compared to duvelisib for patients with 3L+ FL from the perspective of Chinese healthcare system.

Methods: A lifetime three-state partitioned survival model was developed to integrate comparative efficacy and direct costs. An unanchored matching-adjusted indirect comparison (MAIC) was conducted using individual data from NCT04370405 and published aggregate data from the DYNAMO trial, aiming to derive comparative efficacy data and calculate patients' life-years gained. Utility values were from GADOLIN study, as neither trial collected them. Quality-adjusted life-years (QALYs) were calculated by multiplying life-years by utility values. Direct costs included costs of drug acquisition, adverse events, subsequent salvage therapy, health-care resource use (HCRU), and end-of-life care. A 5% annual discount rate was applied to both future QALYs and costs. The primary outcome was the incremental cost-effectiveness ratio (ICER), calculated as discounted incremental costs divided by incremental QALYs. The willingness-to-pay (WTP) threshold was set at China's 2023 per capita GDP (CNY89,358/QALY), with an ICER below this threshold indicating linperlisib was more cost effective. Model robustness was verified via one-way deterministic and probabilistic sensitivity analyses (DSA and PSA).

Results: In the base-case analysis, linperlisib yielded an additional 1.58 QALYs (4.13 vs 2.55) at an incremental cost of CNY108,780 (CNY292,805 vs CNY184,025) compared with duvelisib. The resulting ICER was CNY68,996 per QALY, which was below the WTP. Although drug costs were the main cost driver, improved survival reduced end-of-life care costs by CNY1,507. Deterministic sensitivity analysis identified the price of linperlisib as the top influential parameter, yet all ICERs stayed below the WTP threshold. Probabilistic sensitivity analysis showed a 91.2% cost-effectiveness probability at the preset WTP, confirming robust findings.

Conclusions: Linperlisib is cost effective compared to duvelisib for 3L+ FL patients in China, as verified in sensitivity analyses. Further study is warranted to confirm that it meets an unmet need in China.

PI3K抑制剂治疗中国复发或难治性滤泡性淋巴瘤的成本-效果分析:Linperlisib和Duvelisib的比较
背景:Linperlisib是一种高选择性PI3K-δ抑制剂,于2022年11月在中国首次获批,用于治疗复发或难治性滤泡性淋巴瘤(r/r FL)患者,这些患者之前至少接受过两种全身治疗(3L+ FL),显示出令人满意的临床疗效。目的:本研究旨在从中国医疗体系的角度,评价linperlisib与duvelisib治疗3L+ FL患者的成本-效果。方法:建立一种综合比较疗效和直接成本的终生三状态分区生存模型。使用NCT04370405的个体数据和DYNAMO试验公布的汇总数据进行非锚定匹配调整间接比较(MAIC),旨在获得比较疗效数据并计算患者获得的生命年。效用值来自GADOLIN研究,因为两项试验都没有收集效用值。质量调整寿命年(QALYs)是用寿命年乘以效用值来计算的。直接成本包括药物购买成本、不良事件、后续救助治疗、卫生保健资源使用(HCRU)和临终关怀。5%的年贴现率适用于未来的质量年和成本。主要结局是增量成本-效果比(ICER),计算方法为贴现增量成本除以增量质量比。支付意愿(WTP)阈值设定为中国人均GDP 2023元(89,358元/QALY), ICER低于该阈值表明linperliis更具成本效益。通过单向确定性和概率敏感性分析(DSA和PSA)验证了模型的稳健性。结果:在基本病例分析中,与duvelisib相比,linperlisib产生了额外的1.58个QALYs (4.13 vs 2.55),增量成本为108,780元(292,805元对184,025元)。最终的ICER为68,996元/ QALY,低于WTP。虽然药物成本是主要的成本驱动因素,但生存率的提高使临终关怀成本降低了1,507元。确定性敏感性分析发现,林伯利西布的价格是影响最大的参数,但所有ICERs都低于WTP阈值。概率敏感性分析显示,在预设WTP下,成本-效果概率为91.2%,证实了稳健的研究结果。结论:敏感性分析证实,在中国,与duvelisib相比,Linperlisib对3L+ FL患者具有成本效益。需要进一步的研究来证实它是否满足了中国尚未满足的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书