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A Systematic Review and Methodological Evaluation of Published Cost-Effectiveness Analyses of Aromatase Inhibitors versus Tamoxifen in Early Stage Breast Cancer
被引:15
|作者:
John-Baptiste, Ava A.
[1
,2
,3
,4
,5
]
Wu, Wei
[1
]
Rochon, Paula
[1
,5
,6
]
Anderson, Geoffrey M.
[1
,5
,6
]
Bell, Chaim M.
[5
,6
,7
]
机构:
[1] Womens Coll Hosp, Womens Coll Res Inst, Toronto, ON, Canada
[2] St Michaels Hosp, Keenan Res Ctr, Li Ka Shing Knowledge Inst, Toronto, ON M5B 1W8, Canada
[3] Canc Care Ontario, Pharmacoecon Res Unit, Toronto, ON, Canada
[4] Canadian Ctr Appl Res Canc Control, Toronto, ON, Canada
[5] Inst Clin Evaluat Sci, Toronto, ON, Canada
[6] Univ Toronto, Fac Med, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
[7] Mt Sinai Hosp, Dept Med, Toronto, ON M5G 1X5, Canada
来源:
基金:
加拿大健康研究院;
关键词:
INITIAL ADJUVANT THERAPY;
COMPLETED TREATMENT ANALYSIS;
POSTMENOPAUSAL WOMEN;
HORMONE THERAPIES;
UTILITY ANALYSES;
ATAC ARIMIDEX;
ANASTROZOLE;
LETROZOLE;
CARE;
METAANALYSIS;
D O I:
10.1371/journal.pone.0062614
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Background: A key priority in developing policies for providing affordable cancer care is measuring the value for money of new therapies using cost-effectiveness analyses (CEAs). For CEA to be useful it should focus on relevant outcomes and include thorough investigation of uncertainty. Randomized controlled trials (RCTs) of five years of aromatase inhibitors (AI) versus five years of tamoxifen in the treatment of post-menopausal women with early stage breast cancer, show benefit of AI in terms of disease free survival (DFS) but not overall survival (OS) and indicate higher risk of fracture with AI. Policy-relevant CEA of AI versus tamoxifen should focus on OS and include analysis of uncertainty over key assumptions. Methods: We conducted a systematic review of published CEAs comparing an AI to tamoxifen. We searched Ovid MEDLINE, EMBASE, PsychINFO, and the Cochrane Database of Systematic Reviews without language restrictions. We selected CEAs with outcomes expressed as cost per life year or cost per quality adjusted life year (QALY). We assessed quality using the Neumann checklist. Using structured forms two abstractors collected descriptive information, sources of data, baseline assumptions on effectiveness and adverse events, and recorded approaches to assessing parameter uncertainty, methodological uncertainty, and structural uncertainty. Results: We identified 1,622 citations and 18 studies met inclusion criteria. All CE estimates assumed a survival benefit for aromatase inhibitors. Twelve studies performed sensitivity analysis on the risk of adverse events and 7 assumed no additional mortality risk with any adverse event. Sub-group analysis was limited; 6 studies examined older women, 2 examined women with low recurrence risk, and 1 examined women with multiple comorbidities. Conclusion: Published CEAs comparing AIs to tamoxifen assumed an OS benefit though none has been shown in RCTs, leading to an overestimate of the cost-effectiveness of AIs. Results of these CEA analyses may be suboptimal for guiding policy.
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页数:9
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