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一线细胞周期蛋白依赖性激酶 4/6 抑制剂治疗后的进展:分子机制与临床数据分析。

Progression after First-Line Cyclin-Dependent Kinase 4/6 Inhibitor Treatment: Analysis of Molecular Mechanisms and Clinical Data.

机构信息

Medical Oncology, Oncology Department ASST Lecco, 23900 Lecco, Italy.

School of Medicine and Surgery, University of Milano-Bicocca, 20126 Milano, Italy.

出版信息

Int J Mol Sci. 2023 Sep 22;24(19):14427. doi: 10.3390/ijms241914427.

Abstract

Cyclin-dependent kinase 4/6 inhibitors (CDK4/6iss) are widely used in first-line metastatic breast cancer. For patients with progression under CDK4/6is, there is currently no standard treatment recommended at the category 1 level in international guidelines. The purpose of this article is to review the cellular mechanisms underlying the resistance to CDK4/6is, as well as treatment strategies and the clinical data about the efficacy of subsequent treatments after CDK4/6is-based therapy. In the first part, this review mainly discusses cell-cycle-specific and cell-cycle-non-specific resistance to CDK4/6is, with a focus on early and late progression. In the second part, this review analyzes potential therapeutic approaches and the available clinical data on them: switching to other CDK4/6is, to another single hormonal therapy, to other target therapies (PI3K, mTOR and AKT) and to chemotherapy.

摘要

细胞周期蛋白依赖性激酶 4/6 抑制剂(CDK4/6is)广泛应用于转移性乳腺癌的一线治疗。对于 CDK4/6is 治疗进展的患者,目前国际指南中尚未推荐 1 类水平的标准治疗。本文旨在综述 CDK4/6is 耐药的细胞机制,以及后续治疗策略和 CDK4/6is 治疗后疗效的临床数据。第一部分主要讨论 CDK4/6is 的细胞周期特异性和非特异性耐药,重点讨论早期和晚期进展。第二部分分析了潜在的治疗方法及其临床数据:切换至其他 CDK4/6is、另一种单一激素治疗、其他靶向治疗(PI3K、mTOR 和 AKT)和化疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9553/10572355/5692199d6ed9/ijms-24-14427-g001.jpg

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