Evidence map›Paper›PMID 42304371›Full record

ArticleCost effectiveness and resource allocation : C/E2026

Cost-effectiveness analysis of PET-guided BrECADD with chemotherapy in advanced-stage, classical Hodgkin lymphoma.

Guihao Zeng, Bikun Cai, Hui Zhang, Yuhang Liu, Haonan Li

Registry-linked trialAbstract read
In one paragraph

Article in Cost effectiveness and resource allocation : C/E, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02661503 (HD21 for Advanced Stages Treatment Optimization Trial in the First-line Treatment of Advanced Stage Hodgkin Lymphoma; Comparison of 6 Cycles of Escalated BEACOPP With 6 Cycles of BrECADD), which is not on this map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02661503 phase3unknown statusnot on this map

HD21 for Advanced Stages Treatment Optimization Trial in the First-line Treatment of Advanced Stage Hodgkin Lymphoma; Comparison of 6 Cycles of Escalated BEACOPP With 6 Cycles of BrECADD

TypeinterventionalSponsorUniversity of CologneRan2016 to 2025Enrolled1,500ConditionsClassical Hodgkin LymphomaArmsBleomycin, Etoposide, Doxorubicin, Cyclophosphamide, Vincristine
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Guihao ZengSchool of Medical Business, Guangdong Pharmaceutical University, Guangzhou, Guangdong, China.
Bikun CaiSchool of Medical Business, Guangdong Pharmaceutical University, Guangzhou, Guangdong, China.
Hui ZhangSchool of Medical Business, Guangdong Pharmaceutical University, Guangzhou, Guangdong, China. huizi_zhang@126.com.
Yuhang LiuSchool of Medical Business, Guangdong Pharmaceutical University, Guangzhou, Guangdong, China.
Haonan LiSchool of Pharmaceutical Sciences, Peking University, Beijing, China.

Funding

General Project for Planning Philosophy and Social Sciences in Guangdong Province GD24CGL29General Project of Humanities and Social Science Research for the Ministry of Education 22YJAZH147Guangdong University Innovation Team Project 2022WCXTD011Research team of Pharmacoeconomics and Health Technology Evaluation, Guangdong Pharmaceutical University 2024ZZ13
6 · The paper itself

Abstract

objectiveThe HD21 trial demonstrated efficacy and safety of brentuximab vedotin, etoposide, cyclophosphamide, doxorubicin, dacarbazine, and dexamethasone (BrECADD) vs. bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (eBEACOPP) as frontline therapy for advanced-stage, classical Hodgkin lymphoma. This analysis evaluated the cost-effectiveness of BrECADD from a US healthcare payer perspective.

methodsBuilding upon a multicenter, randomized, open-label phase 3 HD21 trial (NCT02661503) that evaluated BrECADD versus eBEACOPP in advanced-stage, classical Hodgkin lymphoma patients, we constructed a Markov model with 3-week cycles over a 50-year horizon. The model's primary outcomes encompassed total costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratios, with all economic parameters discounted at 3.0% annually. Cost-utility analyses employed a willingness-to-pay threshold of $100,000 per QALY, supplemented by comprehensive sensitivity and scenario analyses to verify model robustness.

resultsEconomic evaluation demonstrated that compared to eBEACOPP, the BrECADD regimen yielded an additional 2.24 QALYs at an incremental cost of $113,134.17, producing an ICER of $50,411.69/QALY, substantially below the $100,000 WTP threshold. One-way sensitivity analysis identified BrECADD drug acquisition costs and health state utility values as the predominant model drivers; all ICERs remained below the $100,000 WTP threshold across the plausible ranges of all parameters. Probabilistic sensitivity analysis indicated that at a willingness-to-pay threshold of $100,000 per QALY, BrECADD was cost-effective compared to eBEACOPP in 100% of 1000 Monte Carlo iterations. The cost-effectiveness acceptability curve demonstrated that BrECADD achieved a greater than 50% probability of being cost-effective at WTP thresholds above approximately $55,000 per QALY.

conclusionsBrECADD can be considered a cost-effective treatment versus eBEACOPP in treating advanced-stage, classical Hodgkin lymphoma in America. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Advanced-stage and classic Hodgkin lymphomaAmericaBrentuximab vedotinChemotherapyCost-effectiveness analysisCost-utility analysis

Identifiers

PMID42304371
PMCPMC13520147

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