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超越标准内分泌治疗:高危早期乳腺癌的一种新辅助治疗方法

Beyond Standard Endocrine Therapy: A New Adjuvant Treatment in High-Risk Early Breast Cancer.

作者信息

Dean Barbara

机构信息

From Carolina Oncology Specialists, Hickory, North Carolina.

出版信息

J Adv Pract Oncol. 2024 Jul 22:1-8. doi: 10.6004/jadpro.2024.15.8.11.

DOI:10.6004/jadpro.2024.15.8.11
PMID:39802529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11715397/
Abstract

The standard adjuvant treatment of estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative early breast cancer (EBC) is endocrine therapy (ET). Despite this treatment, 20% of patients will have their disease recur. Cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors with ET have shown overall survival (OS) benefit in ER-positive, HER2-negative breast cancer in the metastatic setting. Clinical trials are studying the role of oral CDK4/6 inhibitors in the adjuvant treatment of ER-positive, HER2-negative EBC patients who are clinically and pathologically at high risk for recurrence while on standard ET. The monarchE phase III, randomized, controlled trial, looked at one arm of high-risk ER-positive, HER2-negative EBC patients receiving standard ET and the second arm receiving standard ET with a CDK4/6 inhibitor, abemaciclib. Primary endpoint data showed improvement in invasive disease-free survival of 92.2% in the ET and abemaciclib arm vs. 88.7% in the ET arm at 2 years. At 5 years, a preplanned interim analysis showed continued absolute improvement in invasive disease-free survival. Secondary endpoint data for OS have not yet matured. Abemaciclib is approved for use with ET in patients with high-risk, ER-positive, HER2-negative EBC. This article aims to review a case study and the rationale for using oral CDK4/6 inhibitors as adjuvant treatment for this high-risk subset of patients.

摘要

雌激素受体(ER)阳性、人表皮生长因子受体2(HER2)阴性早期乳腺癌(EBC)的标准辅助治疗是内分泌治疗(ET)。尽管有这种治疗方法,但仍有20%的患者疾病会复发。细胞周期蛋白依赖性激酶4和6(CDK4/6)抑制剂联合ET在转移性ER阳性、HER2阴性乳腺癌中已显示出总生存期(OS)获益。临床试验正在研究口服CDK4/6抑制剂在接受标准ET治疗时临床和病理复发风险高的ER阳性、HER2阴性EBC患者辅助治疗中的作用。monarchE III期随机对照试验观察了一组高危ER阳性、HER2阴性EBC患者接受标准ET,另一组接受标准ET联合CDK4/6抑制剂阿贝西利。主要终点数据显示,2年时,ET联合阿贝西利组的无侵袭性疾病生存期改善率为92.2%,而ET组为88.7%。在5年时,一项预先计划的中期分析显示无侵袭性疾病生存期持续有绝对改善。OS的次要终点数据尚未成熟。阿贝西利被批准与ET联合用于高危、ER阳性、HER2阴性EBC患者。本文旨在回顾一个病例研究以及将口服CDK4/6抑制剂用作该高危患者亚组辅助治疗的基本原理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd1/11715397/5a240ba1fef4/jadpro-2024-15-8-11-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd1/11715397/5a240ba1fef4/jadpro-2024-15-8-11-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd1/11715397/5a240ba1fef4/jadpro-2024-15-8-11-g001.jpg

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本文引用的文献

1
Adjuvant Abemaciclib Plus Endocrine Therapy for Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative, High-Risk Early Breast Cancer: Results From a Preplanned monarchE Overall Survival Interim Analysis, Including 5-Year Efficacy Outcomes.辅助阿贝西利联合内分泌治疗激素受体阳性、人表皮生长因子受体 2 阴性、高危早期乳腺癌: monarchE 总生存期中期分析的预先计划结果,包括 5 年疗效结果。
J Clin Oncol. 2024 Mar 20;42(9):987-993. doi: 10.1200/JCO.23.01994. Epub 2024 Jan 9.
2
Abemaciclib plus endocrine therapy for hormone receptor-positive, HER2-negative, node-positive, high-risk early breast cancer (monarchE): results from a preplanned interim analysis of a randomised, open-label, phase 3 trial.阿贝西利联合内分泌治疗激素受体阳性、HER2 阴性、淋巴结阳性、高危早期乳腺癌(monarchE):一项随机、开放标签、III 期临床试验的预先计划的中期分析结果。
Lancet Oncol. 2023 Jan;24(1):77-90. doi: 10.1016/S1470-2045(22)00694-5. Epub 2022 Dec 6.
3
Overall Survival with Palbociclib and Fulvestrant in Women with HR+/HER2- ABC: Updated Exploratory Analyses of PALOMA-3, a Double-blind, Phase III Randomized Study.哌柏西利联合氟维司群治疗 HR+/HER2-ABC 患者的总生存期:PALOMA-3 研究的更新探索性分析,这是一项双盲、III 期随机研究。
Clin Cancer Res. 2022 Aug 15;28(16):3433-3442. doi: 10.1158/1078-0432.CCR-22-0305.
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J Clin Oncol. 2021 May 10;39(14):1518-1530. doi: 10.1200/JCO.20.03639. Epub 2021 Apr 1.