The cost-effectiveness of dacomitinib in first-line treatment of advanced/metastatic epidermal growth factor receptor mutation-positive non-small-cell lung cancer (


Journal

Journal of medical economics
ISSN: 1941-837X
Titre abrégé: J Med Econ
Pays: England
ID NLM: 9892255

Informations de publication

Date de publication:
Historique:
pubmed: 24 3 2021
medline: 30 9 2021
entrez: 23 3 2021
Statut: ppublish

Résumé

Although the benefit of first-line epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) over chemotherapy in A partitioned survival model was developed with three health states: progression-free, post-progression, and death. Progression-free and overall survival curves were used to inform movements between states. Clinical data were taken from randomized trials, compared The base-case analysis showed that dacomitinib accrued a total of 2.10 quality-adjusted life-years (QALYs) at a total cost of Swedish krona (SEK) 874,615. The incremental cost-effectiveness ratio (ICER) for dacomitinib vs afatinib was SEK 461,556 per QALY gained. The ICER of osimertinib vs dacomitinib, where the small QALY gains of the former came at a high additional cost, was SEK 11,444,709. Deterministic and probabilistic sensitivity analyses confirmed the robustness of these results; changes to drug and medical resource use costs and overall survival had the greatest impact on ICER estimates. This model is subject to uncertainty associated with extrapolating long-term treatment effects from shorter trial follow-up periods, although this would also be a limitation when using direct comparison or time-dependent hazard ratios. The NMA was limited by the use of indirect comparison, although sensitivity analyses supported the robustness of our findings. Our model demonstrated that dacomitinib is cost-effective for first-line

Identifiants

pubmed: 33754924
doi: 10.1080/13696998.2021.1901722
doi:

Substances chimiques

Protein Kinase Inhibitors 0
Quinazolinones 0
dacomitinib 5092U85G58
ErbB Receptors EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

447-457

Auteurs

Fredrik O L Nilsson (FOL)

Health and Value Sweden, Pfizer Innovations AB, Stockholm, Sweden.

Peter Gal (P)

Evidence Synthesis, Modeling & Communication, Evidera, Budapest, Hungary.

Ivan Houisse (I)

Evidence Synthesis, Modeling & Communication, Evidera, Budapest, Hungary.

Jasmina I Ivanova (JI)

Global Health Economics and Outcomes Research (Oncology), Pfizer Inc, New York, NY, USA.

Sandra T Asanin (ST)

Oncology Sweden, Pfizer Innovations AB, Stockholm, Sweden.

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Classifications MeSH