Bridging Biomarker Testing to Biomarker-Driven Targeted Therapy: Real-World ESR1 Mutation Testing Patterns and Prevalence in ER+, HER2- Metastatic Breast Cancer.

IF 5.8 3区 医学 Q1 GENETICS & HEREDITY
Chi-Yin Liao, Jincy John, Precious Anyanwu, Manali A Bhave, Francois-Clement Bidard, Tyler Marquart, Francisco Sapunar, Aarti Chawla, Lindsay A Williams
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引用次数: 0

Abstract

Background: The estrogen receptor-positive, human epidermal growth factor receptor 2-negative metastatic breast cancer (MBC) treatment landscape continues to evolve with targeted therapy development. Estrogen receptor 1 (ESR1) testing is recommended at recurrence or each progression event to identify patients for effective therapies. However, there is limited information on testing and mutation patterns in the real world that can inform patient identification in the clinic.

Methods: A retrospective observational study among patients with estrogen receptor-positive, human epidermal growth factor receptor 2-negative MBC who initiated first line (1L) therapy with aromatase inhibitors or selective estrogen receptor degraders ± CDK4/6 inhibitors from 1 January, 2020 to 31 March, 2025, using the Flatiron Health Research Database was conducted. ESR1 testing and mutation positivity rates at 1L to third line initiation, stratified by endocrine-resistant, 1L endocrine-sensitive, and endocrine-sensitive/de novo MBC were descriptively reported.

Results: Overall testing rates varied across subgroups, with one or more ESR1 test per patient in 61.2% of patients with endocrine-resistant MBC (n = 2152), 50.5% in patients with 1L endocrine-sensitive MBC (n = 827), and 43.1% in patients with endocrine-sensitive/de novo MBC (n = 5772). Testing rates at 1L initiation were 36.2% in endocrine-resistant MBC and 19.6% in endocrine-sensitive/de novo MBC. Testing rates were approximately 32% at second line and 25% at third line across subgroups. ESR1 mutation positivity (ESR1m+) rates varied by subgroup at 1L initiation and were highest among patients with endocrine-resistant MBC (24.7%), followed by patients with 1L endocrine-sensitive MBC (6.9%) and patients with endocrine-sensitive/de novo MBC (2.1%). All groups had ESR1m+ rates around 30% at second line initiation and 40% at third line initiation. In an exploratory analysis, ~ 60% of ESR1 tests during 1L were conducted in tissue and ~ 40% in blood.

Conclusions: In this population, real-world ESR1 testing rates were low. One in four patients with endocrine-resistant MBC were ESR1m+ at 1L initiation, ~ 30% were ESR1m+ at second line across subgroups, and ~ 40% were ESR1m+ at third line across subgroups. More blood-based testing at recurrence and progression is recommended in the real world to align with guideline recommendations as ESR1m detection is more sensitive in blood than in tissue.

连接生物标志物检测到生物标志物驱动的靶向治疗:真实世界ESR1突变检测模式和ER+, HER2-转移性乳腺癌的患病率。
背景:雌激素受体阳性、人表皮生长因子受体2阴性的转移性乳腺癌(MBC)的治疗前景随着靶向治疗的发展而不断发展。雌激素受体1 (ESR1)检测建议在复发或每次进展事件,以确定患者的有效治疗。然而,在现实世界中,关于检测和突变模式的信息有限,无法为临床中的患者识别提供信息。方法:利用Flatiron健康研究数据库,对2020年1月1日至2025年3月31日期间,雌激素受体阳性、人表皮生长因子受体2阴性的MBC患者进行first线(1L)治疗,使用芳香化酶抑制剂或选择性雌激素受体降解剂±CDK4/6抑制剂。描述性地报道了ESR1检测和突变阳性率在1L至3线起始,按内分泌抗性、1L内分泌敏感和内分泌敏感/新生MBC分层。结果:各亚组的总体检测率各不相同,61.2%的内分泌耐药MBC患者(n = 2152)、50.5%的内分泌敏感MBC患者(n = 827)和43.1%的内分泌敏感/新生MBC患者(n = 5772)每名患者进行一次或多次ESR1检测。内分泌抗性MBC的1L起始检出率为36.2%,内分泌敏感/新生MBC的1L起始检出率为19.6%。在亚组中,二线和三线的检测率分别约为32%和25%。ESR1突变阳性(ESR1m+)率在1L起始时不同亚组间存在差异,其中内分泌抵抗型MBC患者最高(24.7%),其次是1L内分泌敏感型MBC患者(6.9%)和内分泌敏感/新生型MBC患者(2.1%)。所有组的ESR1m+率在二线起始时约为30%,三线起始时约为40%。在一项探索性分析中,1L期间约60%的ESR1检测在组织中进行,约40%在血液中进行。结论:在该人群中,真实世界ESR1检测率较低。四分之一的内分泌耐药MBC患者在起始时间为1L时为ESR1m+,在二线亚组中约30%为ESR1m+,在三线亚组中约40%为ESR1m+。在现实世界中,由于ESR1m在血液中的检测比在组织中的检测更敏感,建议在复发和进展时进行更多的血液检测,以符合指南的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
2.50%
发文量
53
审稿时长
>12 weeks
期刊介绍: Molecular Diagnosis & Therapy welcomes current opinion articles on emerging or contentious issues, comprehensive narrative reviews, systematic reviews (as outlined by the PRISMA statement), original research articles (including short communications) and letters to the editor. All manuscripts are subject to peer review by international experts.
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