Anti-cancer therapy with cyclin-dependent kinase inhibitors: impact and challenges

被引:10
|
作者
Reinius, Marika A. V. [1 ]
Smyth, Elizabeth [1 ]
机构
[1] Cambridge Univ Hosp NHS Fdn Trust, Dept Oncol, Hills Rd, Cambridge CB2 0QQ, England
来源
关键词
Cancer; cell cycle; combination therapy; cyclin-dependent kinase inhibitor; cyclin-dependent kinase; oncology; treatment resistance; METASTATIC BREAST-CANCER; ADJUVANT ENDOCRINE THERAPY; PHASE IB TRIAL; CDK4/6; INHIBITION; CELL-CYCLE; COMBINATION THERAPY; HEPATOCELLULAR-CARCINOMA; PALBOCICLIB PD-0332991; PREDICTING RESPONSE; CDK6; AMPLIFICATION;
D O I
10.1017/erm.2021.3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The introduction of cyclin-dependent kinase 4/6 inhibitors (CKIs) has marked a major development in the standard treatment of advanced breast cancer. Extensive preclinical, translational and clinical research efforts into CKI agents are ongoing, and clinical application of this class of systemic anti-cancer therapy is anticipated to expand beyond metastatic breast cancer treatment. Emerging evidence indicates that mechanisms by which CKI agents exert their therapeutic effect transcend their initially expected impacts on cell cycle control into the realms of cancer immunology and metabolism. The recent expansion in our understanding of the multifaceted impact of CKIs on tumour biology has the potential to improve clinical study design, therapeutic strategies and ultimately patient outcomes. This review contextualises the current status of CKI therapy by providing an overview of the original and emerging insights into mechanisms of action and the evidence behind their current routine use in breast cancer management. Recent preclinical and clinical studies into CKIs across tumour types are discussed, including a synthesis of the more than 300 clinical trials of CKI-combination treatments registered as of November 2020. Key challenges and opportunities anticipated in the 2020s are explored, including treatment resistance, combination therapy strategies and potential biomarker development.
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页数:22
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