Practical implications of androgen receptor inhibitors for prostate cancer treatment.

Q3 Medicine Exploration of targeted anti-tumor therapy Pub Date : 2024-01-01 Epub Date: 2024-05-28 DOI:10.37349/etat.2024.00234
Fabio Campodonico, Luca Foppiani, Vittoria Campodonico, Carlo Introini
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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 (BRCA). Before undergoing new antiandrogenic therapies, patients should be evaluated for cardiological and metabolic risk and possible drug interactions.

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雄激素受体抑制剂对前列腺癌治疗的实际意义。
抗雄激素一直被用作治疗前列腺癌的单一药物或与激素剥夺疗法联合使用。新一代抗雄激素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。恩扎鲁胺、阿帕鲁胺和达罗鲁胺是新的雄激素受体抑制剂,其耐受性和毒性均可接受,对激素敏感型和阉割耐药型前列腺癌(CRPC)均有活性。目前还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患者个体、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(BRCA)的转移性CRPC患者有效的新药联用,也显示出良好的效果。在接受新的抗雄激素疗法之前,应评估患者的心脏病和代谢风险以及可能的药物相互作用。
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来源期刊
CiteScore
2.80
自引率
0.00%
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0
审稿时长
13 weeks
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