Identifying cost-effective treatment with raloxifene in postmenopausal women using risk algorithms for fractures and invasive breast cancer

被引:20
作者
Ivergard, M. [1 ]
Strom, O. [1 ,2 ]
Borgstrom, F. [1 ,2 ]
Burge, R. T.
Tosteson, A. N. A. [3 ]
Kanis, J. [4 ]
机构
[1] i3 Innovus, S-11164 Stockholm, Sweden
[2] Karolinska Inst, Dept Learning Informat Management & Eth, Med Management Ctr, Stockholm, Sweden
[3] Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Hanover, NH 03756 USA
[4] Univ Sheffield, WHO Collaborating Ctr, Sheffield, S Yorkshire, England
关键词
Cost; Intervention threshold; Osteopenia; Osteoporosis; QALY; FRAX; QUALITY-OF-LIFE; HORMONE REPLACEMENT THERAPY; RANDOMIZED CONTROLLED-TRIAL; ET-AL MODEL; ECONOMIC-EVALUATION; BONE MASS; OSTEOPOROTIC FRACTURES; VENOUS THROMBOEMBOLISM; PULMONARY-EMBOLISM; VERTEBRAL FRACTURE;
D O I
10.1016/j.bone.2010.07.024
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The National Osteoporosis Foundation (NOF) recommends considering treatment in women with a 20% or higher 10-year probability of a major fracture. However, raloxifene reduces both the risk of vertebral fractures and invasive breast cancer so that raloxifene treatment may be clinically appropriate and cost-effective in women who do not meet a 20% threshold risk. The aim of this study was to identify cost-effective scenarios of raloxifene treatment compared to no treatment in younger postmenopausal women at increased risk of invasive breast cancer and fracture risks below 20%. Method: A micro-simulation model populated with data specific to American Caucasian women was used to quantify the costs and benefits of 5-year raloxifene treatment. The population evaluated was selected based on 10-year major fracture probability as estimated with FRAX (R) being below 20% and 5-year invasive breast cancer risk as estimated with the Gail risk model ranging from 1% to 5%. Results: The cost per QALY gained ranged from US $22,000 in women age 55 with 5% invasive breast cancer risk and 15-19.9% fracture probability, to $110,000 in women age 55 with 1% invasive breast cancer risk and 5-9.9% fracture probability. Raloxifene was progressively cost-effective with increasing fracture risk and invasive breast cancer risk for a given age cohort. At lower fracture risk in combination with lower invasive breast cancer risk or when no preventive raloxifene effect on invasive breast cancer was assumed, the cos-teffectiveness of raloxifene worsened markedly and was not cost-effective given a willingness-to-pay of US $50,000. At fracture risk of 15-19.9% raloxifene was cost-effective also in women at lower invasive breast cancer risk. Conclusions: Raloxifene is potentially cost-effective in cohorts of young postmenopausal women, who do not meet the suggested NOF 10-year fracture risk threshold. The cost-effectiveness is contingent on their 5-year invasive breast cancer risk. The result highlights the importance of considering a woman's full risk profile when considering anti-osteoporosis treatment. (C) 2010 Published by Elsevier Inc.
引用
收藏
页码:966 / 974
页数:9
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