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氟维司群治疗未经治疗的激素受体阳性局部晚期或转移性乳腺癌:一项 NICE 单技术评估的证据审查组观点。

Fulvestrant for Untreated Hormone-Receptor Positive Locally Advanced or Metastatic Breast Cancer: An Evidence Review Group Perspective of a NICE Single Technology Appraisal.

机构信息

Southampton Health Technology Assessments Centre, University of Southampton, First Floor, Epsilon House, Enterprise Road, Southampton Science Park, Southampton, SO16 7NS, UK.

出版信息

Pharmacoeconomics. 2019 Jun;37(6):753-762. doi: 10.1007/s40273-018-0725-3.

Abstract

Clinical and cost-effectiveness evidence on fulvestrant for untreated hormone-receptor positive locally advanced or metastatic breast cancer was submitted to the single technology appraisal process of the National Institute for Health and Care Excellence by the manufacturer of fulvestrant. The Southampton Health Technology Assessments Centre was commissioned by the National Institute for Health and Care Excellence as an independent Evidence Review Group to critique the company's submitted evidence. Fulvestrant was compared directly with anastrozole in two randomised controlled trials and was compared indirectly by means of a network meta-analysis with anastrozole, letrozole and tamoxifen. This article summarises the Evidence Review Group's review of the company's submission and summarises the guidance the National Institute for Health and Care Excellence Appraisal Committee issued in January 2018. The Evidence Review Group had several concerns, the most important of which related to the degree to which fulvestrant might confer a benefit in overall survival. This was because mature data were not available from the key phase III trial FALCON. The economic model was sensitive to changes in overall survival and the Evidence Review Group considered the incremental cost-effectiveness ratio was uncertain and likely to increase once mature results from FALCON become available. The National Institute for Health and Care Excellence Appraisal Committee concluded that fulvestrant could not be recommended for treating locally advanced or metastatic estrogen-receptor-positive breast cancer in postmenopausal women who have not received previous endocrine therapy.

摘要

辉瑞公司向英国国家卫生与临床优化研究所提交了未经治疗的激素受体阳性局部晚期或转移性乳腺癌使用氟维司群的临床和成本效益证据。南安普顿健康技术评估中心受英国国家卫生与临床优化研究所委托,作为独立的证据审查小组,对该公司提交的证据进行了评估。氟维司群在两项随机对照试验中与阿那曲唑直接比较,并通过网络荟萃分析与阿那曲唑、来曲唑和他莫昔芬间接比较。本文总结了证据审查小组对该公司提交材料的审查,并总结了英国国家卫生与临床优化研究所评估委员会在 2018 年 1 月发布的指导意见。证据审查小组有几个关注的问题,其中最重要的是氟维司群在总生存方面可能带来的获益程度。这是因为关键的 III 期试验 FALCON 中没有成熟的数据。该经济模型对总生存的变化敏感,证据审查小组认为,一旦 FALCON 的成熟结果可用,增量成本效益比就不确定且可能会增加。英国国家卫生与临床优化研究所评估委员会的结论是,氟维司群不能推荐用于治疗绝经后未接受过内分泌治疗的局部晚期或转移性雌激素受体阳性乳腺癌患者。

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