The Cost-Effectiveness of Frontline Tyrosine Kinase Inhibitors for Patients With Chronic Myeloid Leukemia: In Pursuit of Treatment-Free Remission and Dose Reduction

被引:0
|
作者
Metsemakers, Sanne J. J. P. M. [1 ]
Hermens, Rosella P. M. G. [2 ]
Ector, Genevieve I. C. G. [1 ]
Blijlevens, Nicole M. A. [3 ]
Govers, Tim M. [1 ,4 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Hematol, Nijmegen, Gelderland, Netherlands
[2] Radboud Univ Nijmegen, IQ Hlth, Med Ctr, Nijmegen, Gelderland, Netherlands
[3] Medip Analyt, Nijmegen, Gelderland, Netherlands
[4] Radboud Univ Nijmegen, Dept Med Imaging, Med Ctr, Nijmegen, Gelderland, Netherlands
关键词
chronic myeloid leukemia; dose reduction; economic evaluation; healthcare costs; treatment-free remission; tyrosine kinase inhibitors; quality of life; CHRONIC MYELOGENOUS LEUKEMIA; QUALITY-OF-LIFE; GENERIC IMATINIB; OUTCOMES; CML; THERAPY; RECOMMENDATIONS; IDENTIFICATION; AVAILABILITY; ASSOCIATION;
D O I
10.1016/j.jval.2024.12.005
中图分类号
F [经济];
学科分类号
02 ;
摘要
Objectives: The management of chronic myeloid leukemia (CML) now includes dose reduction (DR) and treatment-free remission (TFR). Evaluating the cost-effectiveness of lifelong-prescribed expensive tyrosine kinase inhibitors (TKIs) for CML is crucial. Prior cost-effectiveness evaluations state that imatinib is the favorable frontline TKI. Some of these evaluations address TFR, but not DR, nor aging and second-generation (2G)-TKIs upcoming patent expirations. This study evaluates the cost-effectiveness of frontline TKIs for CML patients including these factors. Methods: This Markov model evaluates the cost-effectiveness of frontline TKIs for newly diagnosed patients with CML using 17 health states. Transition probabilities, costs, and utilities were derived from literature data. Incremental cost-effectiveness ratios were calculated. Sensitivity analysis and model validation were conducted. Results: Nilotinib is most effective (20.13 quality-adjusted life-years [QALYs]) and imatinib is least effective (17.25 QALYs) for the model including TFR and DR. Imatinib was favored over dasatinib (89.80%), nilotinib (62.70%), and bosutinib (78.40%), at a willingness-to-pay threshold of V80 000 per QALY. Without TFR and DR, fewer QALYs were generated. For patients at the age of 70 years, imatinib has a high probability of being more cost-effective than dasatinib, nilotinib, and bosutinib. With 50% 2GTKI cost reductions, nilotinib is considered more cost-effective compared with imatinib (98.40%), dasatinib (94.80%), and bosutinib (68.90%). Conclusions: The findings indicate that 2GTKIs are more effective in generating QALYs, including for older (age >70 years) patients. Given the current TKI prices, imatinib remains cost-effective. Including DR and TFR in CML management generates more QALYs. Cost reductions from expected 2GTKIs patent expirations will greatly increase their cost-effectiveness. Results may inform 2GTKIs cost discussions after patent expiration, potentially broadening global availability. The findings also emphasize the importance of aiming for TFR and DR in CML management.
引用
收藏
页码:224 / 232
页数:9
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