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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.

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

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