Abstract
Adjuvant zoledronic acid (za) appears to improve disease-free survival (dfs) in women with early-stage breast cancer and low levels of estrogen (lle) because of induced or natural menopause. Characterizing the cost-utility (cu) of this therapy could help to determine its role in clinical practice. Using the perspective of the Canadian health care system, we examined the cu of adjuvant endocrine therapy with or without za in women with early-stage endocrine-sensitive breast cancer and lle. A Markov model was used to compute the cumulative costs in Canadian dollars and the quality-adjusted life-years (qalys) gained from each adjuvant strategy, discounted at a rate of 5% annually. The model incorporated the dfs and fracture benefits of adjuvant za. Probabilistic and one-way sensitivity analyses were conducted to examine key model parameters. Compared with a no-za strategy, adjuvant za in the induced and natural menopause groups was associated with, respectively, $7,825 and $7,789 in incremental costs and 0.46 and 0.34 in qaly gains for cu ratios of $17,007 and $23,093 per qaly gained. In one-way sensitivity analyses, the results were most sensitive to changes in the za dfs benefit. Probabilistic sensitivity analysis suggested a 100% probability of adjuvant za being a cost-effective strategy at a threshold of $100,000 per qaly gained. Based on available data, adjuvant za appears to be a cost-effective strategy in women with endocrine-sensitive breast cancer and lle, having cu ratios well below accepted thresholds.
Highlights
More than 50% of breast cancer patients present with earlystage endocrine-sensitive disease
Marked methodologic heterogeneity has complicated the interpretation of trials examining adjuvant za in early breast cancer
Many of the completed trials investigated adjuvant bisphosphonate therapy for its effect on bone health[7,8,9,10,11,12]. Those trials often compared early with delayed bisphosphonate therapy rather than adjuvant za with no bisphosphonate, or considered primary endpoints that were unrelated to breast cancer outcomes
Summary
More than 50% of breast cancer patients present with earlystage endocrine-sensitive disease. Many of the completed trials investigated adjuvant bisphosphonate therapy for its effect on bone health[7,8,9,10,11,12] Those trials often compared early with delayed bisphosphonate therapy rather than adjuvant za with no bisphosphonate, or considered primary endpoints that were unrelated to breast cancer outcomes. The only two phase iii trials that considered cancer-specific primary endpoints and compared adjuvant therapy with and without za (abcsg-12 and azure) independently suggested that adjuvant za improves breast cancer outcomes in patients with low circulating estrogen levels secondary to induced or natural menopause[13,14]. Adjuvant zoledronic acid (za) appears to improve disease-free survival (dfs) in women with earlystage breast cancer and low levels of estrogen (lle) because of induced or natural menopause. Characterizing the cost–utility (cu) of this therapy could help to determine its role in clinical practice
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