Cost-effectiveness of the Sequential Application of Tyrosine Kinase Inhibitors for the Treatment of Chronic Myeloid Leukemia
Overview
Authors
Affiliations
Several tyrosine kinase inhibitors (TKIs) are approved for chronic myeloid leukemia (CML) therapy. We evaluated the long-term cost-effectiveness of seven sequential therapy regimens for CML in Austria. A cost-effectiveness analysis was performed using a state-transition Markov model. As model parameters, we used published trial data, clinical, epidemiological and economic data from the Austrian CML registry and national databases. We performed a cohort simulation over a life-long time-horizon from a societal perspective. Nilotinib without second-line TKI yielded an incremental cost-utility ratio of 121,400 €/quality-adjusted life year (QALY) compared to imatinib without second-line TKI after imatinib failure. Imatinib followed by nilotinib after failure resulted in 131,100 €/QALY compared to nilotinib without second-line TKI. Nilotinib followed by dasatinib yielded 152,400 €/QALY compared to imatinib followed by nilotinib after failure. Remaining strategies were dominated. The sequential application of TKIs is standard-of-care, and thus, our analysis points toward imatinib followed by nilotinib as the most cost-effective strategy.
Wan Puteh S, Mohamad Selamat E, Aizuddin A, Tumian N, Sathar J Asian Pac J Cancer Prev. 2022; 23(12):4253-4260.
PMID: 36580008 PMC: 9971449. DOI: 10.31557/APJCP.2022.23.12.4253.
Agrawal R, Vieira J, Ryan J, Negi H, Rajput T, Corbin R Pharmacoeconomics. 2022; 40(12):1159-1186.
PMID: 36175789 DOI: 10.1007/s40273-022-01189-9.
Yamamoto C, Nakashima H, Ikeda T, Kawaguchi S, Toda Y, Ito S Blood Adv. 2019; 3(21):3266-3277.
PMID: 31698458 PMC: 6855125. DOI: 10.1182/bloodadvances.2019000745.
How Do We Improve the Impact of Iodine Deficiency Disorders Prevention in Europe and Beyond?.
Volzke H, Erlund I, Hubalewska-Dydejczyk A, Ittermann T, Peeters R, Rayman M Eur Thyroid J. 2018; 7(4):193-200.
PMID: 30283737 PMC: 6140605. DOI: 10.1159/000490347.
Fu J, Liu Y, Lin H, Wu B Clin Drug Investig. 2018; 38(12):1167-1178.
PMID: 30232698 DOI: 10.1007/s40261-018-0706-5.