Venetoclax in Combination with Obinutuzumab in Previously Untreated Fit Patients with Chronic Lymphocytic Leukemia: A Canadian Cost-Utility Analysis.

IF 2.4 Q2 ECONOMICS
PharmacoEconomics Open Pub Date : 2026-01-01 Epub Date: 2025-11-07 DOI:10.1007/s41669-025-00610-1
Gijs van de Wetering, Carolyn Owen, Versha Banerji, Ariane Gosselin, Shivani Kamdar, Nancy Paul Roc, Lytske Bakker, Gargi Ratnaparkhi, Stephane Barakat, Colin Vicente, Beenish S Manzoor
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引用次数: 0

Abstract

Background/objective: Chronic lymphocytic leukemia (CLL) is the most common lymphoproliferative disorder diagnosed in Canada and is associated with a significant economic burden. This study evaluates the cost effectiveness of fixed-treatment duration venetoclax plus obinutuzumab (VEN + O) for previously untreated, fit CLL patients in Canada, for whom this therapy is not universally reimbursed provincially.

Methods: A three-state partitioned survival model was developed using data from the CLL13 trial and a Bayesian network meta-analysis. Health states included progression-free, progressed disease, and death. A lifetime horizon (40-year) was used and a 1.5% discount rate was applied to costs and effects. Costs included drug acquisition, administration, monitoring, adverse events, subsequent treatment, and terminal care. Utility values were derived from previous NICE technology appraisals in CLL. Extensive sensitivity and scenario analyses were conducted.

Results: VEN + O was associated with lower total costs and higher quality-adjusted life years and thus dominant compared with ibrutinib, zanubrutinib, and fludarabine plus cyclophosphamide plus rituximab. Compared with acalabrutinib and venetoclax plus ibrutinib, the incremental cost-utility ratios (ICURs) were in the south-west quadrant and substantially above a CA$50,000/QALY willingness-to-pay threshold, meaning VEN + O was cost effective versus these comparators. VEN + O was cost effective versus bendamustine plus rituximab. Extensive sensitivity and scenario analyses confirmed the robustness of these results.

Conclusions: This analysis demonstrates that VEN + O, a 12-month fixed duration treatment, is a cost-effective option for previously untreated fit CLL patients in Canada. VEN + O offers potential health benefits and cost savings when compared with relevant comparator treatments.

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Venetoclax联合Obinutuzumab治疗未治疗的慢性淋巴细胞白血病患者:加拿大的成本-效用分析
背景/目的:慢性淋巴细胞白血病(CLL)是加拿大诊断出的最常见的淋巴增生性疾病,并与重大的经济负担相关。本研究评估了固定治疗时间venetoclax + obinutuzumab (VEN + O)对加拿大未接受治疗的适合CLL患者的成本效益,该治疗在各省没有普遍报销。方法:利用CLL13试验数据和贝叶斯网络元分析建立三状态分区生存模型。健康状态包括无进展、疾病进展和死亡。使用寿命期限(40年),对成本和效果采用1.5%的贴现率。费用包括药物购置、给药、监测、不良事件、后续治疗和临终护理。效用值来源于以前NICE在CLL中的技术评价。进行了广泛的敏感性和情景分析。结果:VEN + O与较低的总成本和较高的质量调整生命年相关,因此与依鲁替尼、扎鲁替尼和氟达拉滨+环磷酰胺+利妥昔单抗相比具有优势。与acalabrutinib和venetoclax + ibrutinib相比,增量成本效用比(ICURs)位于西南象限,并且大大高于50,000加元/QALY的支付意愿阈值,这意味着VEN + O与这些比较物相比具有成本效益。与苯达莫司汀+利妥昔单抗相比,VEN + O具有成本效益。广泛的敏感性和情景分析证实了这些结果的稳健性。结论:该分析表明,VEN + O,一种12个月的固定疗程治疗,是加拿大先前未治疗的适合CLL患者的成本效益选择。与相关比较治疗相比,VEN + O提供潜在的健康益处和成本节约。
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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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