达piciclib治疗乳腺癌的进展综述。

IF 3.4 4区 医学 Q2 ONCOLOGY
Breast Cancer : Targets and Therapy Pub Date : 2025-06-30 eCollection Date: 2025-01-01 DOI:10.2147/BCTT.S529794
Zhimin Chen, Pengjun Xie, Qihai Chen, Jie Ouyang
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引用次数: 0

摘要

细胞周期蛋白依赖性激酶4和6抑制剂(CDK4/6抑制剂)与细胞周期蛋白依赖性蛋白联合可减少细胞周期蛋白D-CDK4/6复合物的形成,导致下游基因失活,抑制细胞增殖。先前的研究表明,CDK4/6抑制剂与内分泌疗法和抗her2靶向药物联合应用于不同亚型和分期的乳腺癌,在患者预后和耐受药物毒性方面显示出有希望的结果。目前,广泛应用于乳腺癌治疗的CDK4/6抑制剂有palbociclib、abemaciclib和ribociclib。Dalpiciclib (SHR6390)是中国研发的新型CDK4/6选择性抑制剂,已获得国家药品监督管理局批准上市。目前正在对达匹昔利布与不同抗肿瘤药物的疗效进行研究,探讨达匹昔利布的最佳使用策略。本文就dalpiciclib在不同乳腺癌亚型、不同抗肿瘤药物、不同治疗时机的研究进展进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancements in Dalpiciclib for the Treatment of Breast Cancer Patients: A Review.

Combining cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6 inhibitors) with cyclin-dependent proteins can reduce the formation of cyclin D-CDK4/6 complexes, resulting in the inactivation of downstream genes and suppression of cell proliferation. Previous research on the use of CDK4/6 inhibitors in combination with endocrine therapies and anti-HER2 targeting agents across various subtypes and stages of breast cancer has shown promising outcomes in patient prognoses and tolerable drugs toxicities. For the present, the CDK4/6 inhibitors that have been widely used for the treatment of breast cancer are palbociclib, abemaciclib and ribociclib. Dalpiciclib (SHR6390), a novel and selective CDK4/6 inhibitor developed in China, has been approved by the National Medical Products Administration. The researches about dalpiciclib with different anti-tumor drugs are ongoing to explore the efficacy and the best strategies to use dalpiciclib. This review provides an overview of the research progress on dalpiciclib across different breast cancer subtypes with various anti-tumor drugs in different treatment opportunities.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
40
审稿时长
16 weeks
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