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双相雄激素疗法对伴有肿瘤抑制因子联合缺失的转移性去势抵抗性前列腺癌男性患者的临床疗效

Clinical Efficacy of Bipolar Androgen Therapy in Men with Metastatic Castration-Resistant Prostate Cancer and Combined Tumor-Suppressor Loss.

作者信息

Markowski Mark C, Wang Hao, De Marzo Angelo M, Schweizer Michael T, Antonarakis Emmanuel S, Denmeade Samuel R

机构信息

Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, USA.

Department of Biostatistics, Johns Hopkins School of Medicine, Baltimore, MD, USA.

出版信息

Eur Urol Open Sci. 2022 Jun 3;41:112-115. doi: 10.1016/j.euros.2022.05.006. eCollection 2022 Jul.

Abstract

UNLABELLED

Bipolar androgen therapy (BAT) relies on oscillating levels of serum testosterone as a way to treat patients with metastatic castration-resistant prostate cancer (mCRPC). Aggressive-variant prostate cancers typically require combination chemotherapy and are frequently associated with loss-of-function mutations in tumor suppressor genes. Here we report clinical outcomes after BAT among patients with mCRPC harboring pathogenic alterations in at least two of three genes: , and In this setting, BAT induced a meaningful PSA response rate, progression-free survival and overall survival, particularly in patients without prior chemotherapy.

PATIENT SUMMARY

Bipolar androgen therapy, in which drugs are used to raise testosterone levels and then allow them to decrease again in a cycle, may be a safe and effective treatment for prostate cancer that is resistant to testosterone suppression and has mutations in tumor suppressor genes. A randomized study comparing this approach to chemotherapy is needed to confirm the findings.

摘要

未标注

双相雄激素疗法(BAT)依靠血清睾酮水平的波动来治疗转移性去势抵抗性前列腺癌(mCRPC)患者。侵袭性变异型前列腺癌通常需要联合化疗,且常与肿瘤抑制基因的功能丧失性突变相关。在此,我们报告了在三个基因( 、 和 )中至少有两个存在致病性改变的mCRPC患者接受BAT后的临床结果。在这种情况下,BAT诱导了有意义的前列腺特异性抗原(PSA)反应率、无进展生存期和总生存期,尤其是在未接受过化疗的患者中。

患者总结

双相雄激素疗法是使用药物提高睾酮水平,然后使其再次下降形成一个循环,对于对睾酮抑制有抗性且肿瘤抑制基因有突变的前列腺癌可能是一种安全有效的治疗方法。需要进行一项将该方法与化疗进行比较的随机研究来证实这些发现。

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