口服 SERDs 单独或与 CDK 4/6 抑制剂联合治疗乳腺癌:当前视角与临床试验

IF 5.7 2区 医学 Q1 OBSTETRICS & GYNECOLOGY Breast Pub Date : 2024-04-04 DOI:10.1016/j.breast.2024.103729
Kleoniki Apostolidou, Eleni Zografos, Maria Alkistis Papatheodoridi, Oraianthi Fiste, Meletios Athanasios Dimopoulos, Flora Zagouri
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引用次数: 0

摘要

过去几十年来,由于采用了细胞周期蛋白依赖性激酶4/6抑制剂(CDK 4/6i)辅助内分泌治疗,治疗晚期和转移性HR+/HER2-乳腺癌的一线疗法发生了转变。然而,对具有卓越疗效的新型内分泌疗法的需求仍未得到满足,以改善治疗效果并克服CDK4/6i耐药性。口服给药且生物利用度更高的新一代选择性雌激素受体降解剂(SERD)有可能成为满足这一新兴需求的新型化合物。在本文中,我们回顾了有关 CDK4/6 抑制剂和口服 SERDs 联合作用的已获认可的临床研究,报告了已有的疗效数据,并为未来以这些有前景的药物为重点的研究提供了一个框架。
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Oral SERDs alone or in combination with CDK 4/6 inhibitors in breast cancer: Current perspectives and clinical trials

Over the past few decades, first-line therapy for treating advanced and metastatic HR+/HER2-breast cancer has transformed due to the introduction of adjuvant endocrine therapy with cyclin-dependent kinase 4/6 inhibitors (CDK 4/6i). However, there is an unmet need for novel classes of endocrine therapy with superior efficacy to improve treatment outcomes and overcome CDK4/6i resistance. New generation selective estrogen receptor degraders (SERDs), orally administered and with higher bioavailability, could potentially be the novel compounds to meet this emerging need. In this paper, we review accredited clinical studies on the combining effects of CDK4/6 inhibitors and oral SERDs, report efficacy of treatment data when available, and provide a framework for future research focusing on these promising agents.

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来源期刊
Breast
Breast 医学-妇产科学
CiteScore
8.70
自引率
2.60%
发文量
165
审稿时长
59 days
期刊介绍: The Breast is an international, multidisciplinary journal for researchers and clinicians, which focuses on translational and clinical research for the advancement of breast cancer prevention, diagnosis and treatment of all stages.
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