Economic Evaluations of Emerging Genomic Tests for Early Stage Breast Cancer
Economic Evaluations of Emerging Genomic Tests for Early Stage Breast Cancer
批准号:
7256700
负责人:
Ya-Chen Tina Shih
金额:
$7.7万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-03-15 至 2009-02-28
关键词:
ClinicalEarly treatmentEconomicsEvaluationGenomeGenomicsHealthHealthcareHumanHuman Genome ProjectLicensingMedical TechnologyMethodsNumbersPatientsPerformancePharmacogenomicsPhysiciansPurposeRangeSafetySocietiesStagingTechnologyTestingWomanbasecostcost effectivenessimprovedinnovationmalignant breast neoplasmperformance testsprognostic
中文摘要
描述(由申请人提供):新兴的医疗技术正在大幅改善我们的医疗保健选择,但往往会带来相当大的额外成本。成本效益和可负担性被描述为新医疗技术的第四和第五个障碍,仅次于传统的许可要求的三个障碍:安全性、有效性和质量。人类基因组计划提供了充分的机会,通过创新的基于基因组的技术来改善人类健康,这些技术最近才出现。已经开发了许多基因组预后和预测测试,以帮助医生为早期乳腺癌(ESBC)患者提供更好的治疗。这些新兴的基因组测试的临床应用不仅取决于测试的准确性,还取决于它们对社会的经济影响。这项研究的目的是使用经济评估方法,在成本效益和可负担性的背景下,检查药物基因组预测和预测测试的性能和它们在可信范围内的测试性能和成本之间的关系,以及ESBC患者的成本。具体目标如下:
1.比较药物基因组学预后试验与目前治疗ESBC的方法的成本-效果
2.评估在ESBC治疗中使用药物基因组预测试验与当前做法的成本效益
3.评价药物基因组学预测试验和预测试验相结合治疗ESBC的成本效益。
4.评估新出现的药物基因组预测和/或预测试验的预算影响
英文摘要
DESCRIPTION (provided by applicant): Emerging medical technologies are substantially improving our health care options, but often at considerable added cost. Cost-effectiveness and affordability are described as the fourth and fifth hurdles for new medical technologies, following the traditional three hurdles for licensing requirements: safety, efficacy, and quality. The Human Genome Project offers ample opportunity to improve human health through innovative genome-based technologies that have only recently become available. A number of genomic prognostic and predictive tests have been developed to assist physicians in providing better treatment for patients with early-stage breast cancer (ESBC). Clinical use of these emerging genomic tests will depend not only on the accuracy of the tests but also on their economic impacts to the society. The purpose of this study is to use methods of economic evaluation to examine the relationship between the performance of pharmacogenomic prognostic and predictive tests and their costs over a plausible range of test performance and costs for women with ESBC in the context of costeffectiveness and affordability. The specific aims are the following:
1. To compare the cost-effectiveness of using pharmacogenomic prognostic tests versus current practices in the treatment of ESBC
2. To assess the cost-effectiveness of using pharmacogenomic predictive tests versus current practices in the treatment of ESBC
3. To evaluate the cost-effectiveness of using a combination of pharmacogenomic prognostic and predictive tests versus current practices in the treatment of ESBC
4. To estimate the budgetary impact of the emerging pharmacogenomic prognostic and/or predictive tests
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海外基金