Cost effectiveness of therapeutic drug monitoring for imatinib administration in chronic myeloid leukemia

English version

Autoři: Kibum Kim ^aff001; Gwendolyn A. McMillin ^aff001; Philip S. Bernard ^aff001; Srinivas Tantravahi ^aff003; Brandon S. Walker ^aff001; Robert L. Schmidt ^aff001
Působiště autorů: Department of Pathology and ARUP Laboratories, University of Utah, Salt Lake City, Utah, United States of America ^aff001; Department of Pharmacy, Pharmacotherapy Outcomes Research Center, University of Utah, Salt Lake City, Utah, United States of America ^aff002; Department of Internal Medicine, Division of Hematology and Hematological Malignancies, University of Utah, Salt Lake City, Utah, United States of America ^aff003
Vyšlo v časopise: PLoS ONE 14(12)
Kategorie: Research Article
doi: https://doi.org/10.1371/journal.pone.0226552

Souhrn

Background

Imatinib mesylate (IM) is a first-line treatment option for patients with chronic myeloid leukemia (CML). Patients who fail or are intolerant to IM therapy are treated with more expensive second and third-generation tyrosine kinase inhibitors. Patients show wide variation in trough concentrations in response to standard dosing. Thus, many patients receive subtherapeutic or supratherapeutic doses. Therapeutic drug monitoring (TDM) may improve dose management that, in turn, may reduce costs and improve outcomes. However, TDM also adds to the cost of patient care. The objective of this study was to determine the cost-effectiveness of TDM for generic IM therapy.

Methods

We developed a microsimulation model for the trough plasma concentration of IM which is related to a cytogenetic or molecular response. We compared two cohorts: one with TDM and one without TDM (NTDM). The lifetime incremental cost-effectiveness ratio (ICER) was calculated using quality-adjusted life years (QALYs) as the effectiveness measure. One-way and probabilistic sensitivity analyses were performed.

Results

The lifetime cost and QALY of treatment with TDM were $2,137K [95% Ci: 2,079K; 2,174K] and 12.37 [95% CI: 12.07; 12.55], respectively. The cost and QALY of NTDM were $2,132K [95% CI: 2,091K; 2,197K] and 12.23 [95% CI: 11.96; 12.50], respectively. The incremental cost and QALY for TDM relative to NTDM was $4,417 [95% CI: -52,582; 32,097]) and 0.15 [95% CI: -0.13; 0.28]. The ICER for TDM relative to NTDM was $30,450/QALY. Probabilistic sensitivity analysis showed that TDM was cost-effective relative to NTDM in 90% of the tested scenarios at a willingness-to-pay threshold of $100,000/QALY.

Conclusions

Although the impact of TDM is modest, the cost-effectiveness over a lifetime horizon (societal perspective, ($30,450/QALY) falls within the acceptable range (< $100k/QALY).

Klíčová slova:

Cost-effectiveness analysis – Death rates – Hematology – Hematopoietic stem cell transplantation – Chemotherapy – Pharmacokinetics – Therapeutic drug monitoring – Tyrosine kinase inhibitors

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Cost effectiveness of therapeutic drug monitoring for imatinib administration in chronic myeloid leukemia

Souhrn

Background

Methods

Results

Conclusions

Klíčová slova:

Zdroje

PLOS One

Svět praktické medicíny 3/2024 (znalostní test z časopisu)

Kardiologické projevy hypereozinofilií

Střevní příprava před kolonoskopií

Aktuální možnosti diagnostiky a léčby litiáz

Závislosti moderní doby – digitální závislosti a hypnotika