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[前列腺癌的抗激素治疗:副作用]

[Antihormonal therapy in prostate cancer : Side effects].

作者信息

Ohlmann C H, Thelen P

机构信息

Klinik für Urologie und Kinderurologie, Universität des Saarlandes, 66421, Homburg/Saar, Deutschland.

Klinik für Urologie, Universitätsmedizin Göttingen, 37099 Göttingen, Deutschland.

出版信息

Urologe A. 2017 Apr;56(4):465-471. doi: 10.1007/s00120-017-0340-5.

DOI:10.1007/s00120-017-0340-5
PMID:28246761
Abstract

Androgen deprivation is still standard therapy for prostate cancer, either as primary androgen deprivation therapy or with the use of secondary hormonal drugs including abiraterone and enzalutamide. However, especially the clinically occult side effects like metabolic changes or cardiovascular complications and effects on the psyche of the patient are often not recognized in daily practice. Active monitoring of such side effects is essential for prevention and early intervention. In addition, the efficacy of androgen deprivation therapies is limited by primary and secondary resistance. The underlying molecular mechanism including splice variants of the androgen receptor in contrast to mutations are usually reversible and should be regarded as a sign of efficacy of the current treatment. Therefore, the clever, timely use of androgen deprivation or even the use of a bipolar androgen therapy should enable reversal of resistance to again render tumor cells sensitive to androgen-deprivation therapy.

摘要

雄激素剥夺疗法仍然是前列腺癌的标准治疗方法,无论是作为主要的雄激素剥夺疗法,还是使用包括阿比特龙和恩杂鲁胺在内的二线激素药物。然而,特别是代谢变化或心血管并发症等临床隐匿性副作用以及对患者心理的影响,在日常实践中往往未被认识到。对此类副作用进行积极监测对于预防和早期干预至关重要。此外,雄激素剥夺疗法的疗效受到原发性和继发性耐药性的限制。与突变相反,包括雄激素受体剪接变体在内的潜在分子机制通常是可逆的,应被视为当前治疗疗效的标志。因此,巧妙、及时地使用雄激素剥夺疗法,甚至使用双相雄激素疗法,应能使耐药性逆转,再次使肿瘤细胞对雄激素剥夺疗法敏感。

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Safety and Therapeutic Profile of a GnRH-Based Vaccine Candidate Directed to Prostate Cancer. A 10-Year Follow-Up of Patients Vaccinated With Heberprovac.一种针对前列腺癌的基于促性腺激素释放激素(GnRH)的候选疫苗的安全性和治疗概况。对接种赫伯普罗瓦克疫苗的患者进行的10年随访。
Front Oncol. 2019 Feb 25;9:49. doi: 10.3389/fonc.2019.00049. eCollection 2019.

本文引用的文献

1
Re: Christof Bernemann, Thomas J. Schnoeller, Manuel Luedeke, et al. Expression of AR-V7 in Circulating Tumour Cells Does Not Preclude Response to Next Generation Androgen Deprivation Therapy in Patients with Castration Resistant Prostate Cancer. Eur Urol 2017;71:1-3.
Eur Urol. 2017 Apr;71(4):e105-e106. doi: 10.1016/j.eururo.2016.09.021. Epub 2016 Sep 20.
2
Loss of CHD1 causes DNA repair defects and enhances prostate cancer therapeutic responsiveness.CHD1的缺失会导致DNA修复缺陷并增强前列腺癌的治疗反应性。
EMBO Rep. 2016 Nov;17(11):1609-1623. doi: 10.15252/embr.201642352. Epub 2016 Sep 5.
3
EAU-ESTRO-SIOG Guidelines on Prostate Cancer. Part II: Treatment of Relapsing, Metastatic, and Castration-Resistant Prostate Cancer.EAU-ESTRO-SIOG 前列腺癌诊治指南。第二部分:复发、转移和去势抵抗性前列腺癌的治疗。
Eur Urol. 2017 Apr;71(4):630-642. doi: 10.1016/j.eururo.2016.08.002. Epub 2016 Aug 31.
4
Critical role of androgen receptor level in prostate cancer cell resistance to new generation antiandrogen enzalutamide.雄激素受体水平在前列腺癌细胞对新一代抗雄激素恩杂鲁胺耐药中的关键作用。
Oncotarget. 2016 Sep 13;7(37):59781-59794. doi: 10.18632/oncotarget.10926.
5
[Use of GnRH antagonists versus agonists].
Urologe A. 2016 Sep;55(9):1238-9. doi: 10.1007/s00120-016-0194-2.
6
C-terminally truncated constitutively active androgen receptor variants and their biologic and clinical significance in castration-resistant prostate cancer.C 末端截短的组成型活性雄激素受体变体及其在去势抵抗性前列腺癌中的生物学和临床意义
J Steroid Biochem Mol Biol. 2017 Feb;166:38-44. doi: 10.1016/j.jsbmb.2016.06.008. Epub 2016 Jun 21.
7
Bipolar Androgen Therapy for Men With Androgen Ablation Naïve Prostate Cancer: Results From the Phase II BATMAN Study.双相雄激素疗法用于初治雄激素剥夺的前列腺癌男性患者:II期蝙蝠侠研究结果
Prostate. 2016 Sep;76(13):1218-26. doi: 10.1002/pros.23209. Epub 2016 Jun 24.
8
Brachyury as a potential modulator of androgen receptor activity and a key player in therapy resistance in prostate cancer.短尾相关蛋白作为雄激素受体活性的潜在调节因子以及前列腺癌治疗耐药性中的关键因素。
Oncotarget. 2016 May 17;7(20):28891-902. doi: 10.18632/oncotarget.8499.
9
Functional analysis of androgen receptor mutations that confer anti-androgen resistance identified in circulating cell-free DNA from prostate cancer patients.对在前列腺癌患者循环游离DNA中鉴定出的赋予抗雄激素抗性的雄激素受体突变进行功能分析。
Genome Biol. 2016 Jan 26;17:10. doi: 10.1186/s13059-015-0864-1.
10
Inhibition of FOXC2 restores epithelial phenotype and drug sensitivity in prostate cancer cells with stem-cell properties.抑制FOXC2可恢复具有干细胞特性的前列腺癌细胞的上皮表型和药物敏感性。
Oncogene. 2016 Nov 17;35(46):5963-5976. doi: 10.1038/onc.2015.498. Epub 2016 Jan 25.