医学
螺内酯
前列腺癌
醋酸阿比特龙酯
抗雄激素
雄激素
雄激素受体
盐皮质激素受体
内科学
阿比曲酮
肿瘤科
癌症
泌尿科
内分泌学
药理学
醛固酮
雄激素剥夺疗法
激素
作者
Bert Dhondt,Sarah Buelens,Jeroen Van Besien,Matthias Beysens,Elise De Bleser,Piet Ost,Nicolaas Lumen
标识
DOI:10.1080/17843286.2018.1543827
摘要
Objectives: Disease progression in metastatic castration-resistant prostate cancer (mCRPC) is dependent on androgen signaling. This case describes the complex adaptive androgen signaling mechanisms in mCRPC and illustrates that caution should be exercised when treating these patients with drugs influencing the androgen axis.Methods: Single case report and review of the literature.Results: We report the case of an 86-year-old man with mCRPC, treated with the secondary antihormonal agent abiraterone acetate. Following association of spironolactone to deal with symptoms related to mineralocorticoid excess, biochemical and radiographic disease progression occurred. Spironolactone was discontinued and 8 months after withdrawal, the patient continues to show a biochemical response to abiraterone.Conclusions: Although spironolactone generally exerts anti-androgenic effects, experimental evidence exists that it acts as an androgen receptor agonist in an androgen-depleted environment, capable of inducing prostate cancer proliferation. This is supported by the observations described in this case report. Therefore, spironolactone should be avoided in prostate cancer patients suffering from treatment-associated side effects of abiraterone.
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