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CDK4/6抑制剂在转移性去势抵抗性前列腺癌中的新型治疗策略

Novel Therapeutic Strategies for CDK4/6 Inhibitors in Metastatic Castrate-Resistant Prostate Cancer.

作者信息

Kase Adam M, Copland Iii John A, Tan Winston

机构信息

Mayo Clinic Florida Division of Hematology Oncology, Jacksonville, FL 32224, USA.

Mayo Clinic Florida Department of Cancer Biology, Jacksonville, FL 32224, USA.

出版信息

Onco Targets Ther. 2020 Oct 15;13:10499-10513. doi: 10.2147/OTT.S266085. eCollection 2020.

Abstract

The majority of patients with castrate-resistant prostate cancer will have metastatic disease at the time of diagnosis. Investigative efforts on new therapeutics for this patient population have improved with the development of androgen signaling inhibitors, such as abiraterone and enzalutamide, and PARP inhibitors, such as rucaparib and olaparib, to accompany the previously FDA-approved docetaxel, cabazitaxel, sipuleucel-T, and Radium 223. However, new therapeutic strategies are necessary to prolong survival as progression after these agents is inevitable. CDK4/6 inhibitors have advanced the field of estrogen receptor positive breast cancer treatment and are being investigated in prostate cancer given the role of androgen receptor signaling effects on the cell cycle. Response to CDK4/6 inhibitors may be predicted by the tumors' genomic profile and may provide insight into combinatory therapy with CDK4/6 inhibitors in order to delay resistance or provide synergistic effects. Here, we review the use of CDK4/6 inhibitors in prostate cancer and potential combinations based on known resistance mechanisms to CDK4/6 inhibitors, prostate cancer regulatory pathways, and prostate-cancer-specific genomic alterations.

摘要

大多数去势抵抗性前列腺癌患者在诊断时就已发生转移。随着雄激素信号抑制剂(如阿比特龙和恩杂鲁胺)以及PARP抑制剂(如鲁卡帕尼和奥拉帕尼)的研发,针对这一患者群体的新疗法研究取得了进展,此前美国食品药品监督管理局(FDA)已批准多西他赛、卡巴他赛、西普拉赛特-T和镭-223用于治疗。然而,由于使用这些药物后疾病进展不可避免,因此需要新的治疗策略来延长生存期。CDK4/6抑制剂推动了雌激素受体阳性乳腺癌治疗领域的发展,鉴于雄激素受体信号对细胞周期的作用,目前正在前列腺癌中进行研究。对CDK4/6抑制剂的反应可通过肿瘤的基因组特征来预测,这可能为CDK4/6抑制剂联合治疗提供思路,以延缓耐药或产生协同效应。在此,我们综述了CDK4/6抑制剂在前列腺癌中的应用以及基于已知的CDK4/6抑制剂耐药机制、前列腺癌调控途径和前列腺癌特异性基因组改变的潜在联合用药方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abdf/7576355/45a06d49ec4a/OTT-13-10499-g0001.jpg

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