Cost-Effectiveness Analysis of Treating Acute Promyelocytic Leukemia Patients With Arsenic Trioxide and Retinoic Acid in the United States

被引:16
作者
Tallman, Martin [1 ]
Lo-Coco, Francesco [2 ]
Barnes, Gisoo [3 ]
Kruse, Morgan [4 ]
Wildner, Rebecca [5 ]
Martin, Monique [5 ]
Mueller, Udo [6 ]
Tang, Boxiong [3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[2] Univ Tor Vergata, Via Montpellier 1, I-00133 Rome, Italy
[3] Teva Pharmaceut, Frazer, PA USA
[4] Optum, Waltham, MA USA
[5] MAPI, Uxbridge, Middx, England
[6] Teva Pharmaceut, Ulm, Germany
关键词
Acute promyelocytic leukemia; All-trans retinoic acid; Arsenic trioxide; Cost-effectiveness; Markov model; CHRONIC LYMPHOCYTIC-LEUKEMIA; RISK-ADAPTED TREATMENT; THERAPY; ANTHRACYCLINE; CHEMOTHERAPY; REMISSION; MULTICENTER; INTERGROUP; SURVIVAL; UTILITY;
D O I
10.1016/j.clml.2015.07.634
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A Markov cohort model was used to estimate the cost-effectiveness of arsenic trioxide (ATO) added to all-trans retinoic acid (ATRA) when used in first-line acute promyelocytic leukemia (APL) treatment. Results indicated that the ATO + ATRA regimen is highly cost-effective compared to ATRA + cytarabine + additional chemotherapy or ATRA Didarubicin in the treatment of newly diagnosed low-to intermediate-risk APL patients. Introduction: This study estimated the cost-effectiveness of arsenic trioxide (ATO) added to all-trans retinoic acid (ATRA) when used in first-line acute promyelocytic leukemia (APL) treatment. Materials and Methods: A Markov cohort model was developed with 3 states: stable disease (during first-or second-line treatment), disease event, and death. Newly diagnosed patients with low-to intermediate-risk APL were included and each month could remain in their current health state or move to another. Treatment consisted of ATO + ATRA, ATRA + idarubicin (IDA), or ATRA + cytarabine (AraC) + additional chemotherapy. After an initial disease event, patients discontinued first-line therapy and switched to a second-line ATO regimen. Efficacy and safety data were obtained from published trials; quality of life/utility estimates were obtained from the literature; costs were obtained from US data sources. Costs and outcomes over time were used to calculate incremental cost-effectiveness ratios (ICERs). Deterministic and probabilistic sensitivity analyses were conducted. Results: Compared to ATRA + AraC + additional chemotherapy, ATRA + IDA treatment had ICERs of $2933 per life-year (LY) saved and $3122 per quality-adjusted life-year (QALY) gained. Compared to the ATRA + IDA regimen, first-line ATO + ATRA treatment had ICERs of $4512 per LY saved and $5614 per QALY gained. Results were sensitive to changes in pharmacy costs of the ATO + ATRA regimen during consolidation. Conclusion: The ATO + ATRA regimen is highly cost-effective compared to ATRA + AraC + additional chemotherapy or ATRA + IDA in the treatment of newly diagnosed low-to intermediate-risk APL patients. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:771 / 777
页数:7
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