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雄激素受体抑制剂在前列腺癌治疗中的实际应用

Practical implications of androgen receptor inhibitors for prostate cancer treatment.

作者信息

Campodonico Fabio, Foppiani Luca, Campodonico Vittoria, Introini Carlo

机构信息

Department of Abdominal Surgery, Urology Unit, Galliera Hospital, 16128 Genova, Italy.

Internal Medicine, Galliera Hospital, 16128 Genova, Italy.

出版信息

Explor Target Antitumor Ther. 2024;5(3):543-550. doi: 10.37349/etat.2024.00234. Epub 2024 May 28.

Abstract

Antiandrogens have been used for the treatment of prostate cancer as a single agent or in combination with hormone deprivation therapy. New generation antiandrogens act like androgen receptor inhibitors (ARIs). Their binding complex blocks the pathways of cellular proliferation and differentiation of the prostate. Enzalutamide, apalutamide and darolutamide are the new ARIs that demonstrated acceptable tolerability and toxicity, both active in hormone-sensitive and castration-resistant prostate cancer (CRPC). There is no evidence of superiority of one drug over the other, therefore the therapeutic choice depends on the safety profile in relation to the individual patient, their comorbidities and clinical condition. ARIs have also shown promising results in association with new drugs that are active on patients with metastatic CRPC carrying the mutated breast cancer gene (). Before undergoing new antiandrogenic therapies, patients should be evaluated for cardiological and metabolic risk and possible drug interactions.

摘要

抗雄激素药物已被用作单一药物或与激素剥夺疗法联合用于前列腺癌的治疗。新一代抗雄激素药物的作用类似于雄激素受体抑制剂(ARIs)。它们的结合复合物会阻断前列腺细胞增殖和分化的途径。恩杂鲁胺、阿帕鲁胺和达罗他胺是新型ARIs,已证明具有可接受的耐受性和毒性,对激素敏感性和去势抵抗性前列腺癌(CRPC)均有效。没有证据表明一种药物优于另一种药物,因此治疗选择取决于与个体患者、其合并症和临床状况相关的安全性。ARIs与对携带突变乳腺癌基因的转移性CRPC患者有效的新药联合使用时也显示出了有前景的结果。在接受新的抗雄激素治疗之前,应对患者进行心脏和代谢风险以及可能的药物相互作用评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b351/11220289/4179f328cad8/etat-05-1002234-g001.jpg

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