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醋酸阿比特龙持续用于一名缓解期前列腺癌患者导致肾上腺功能不全:无皮质类固醇监测的长期治疗的风险。

Adrenal Insufficiency Induced by Continued Abiraterone Acetate Use in a Prostate Cancer Patient in Remission: The Dangers of Unmonitored Long-Term Therapy Without Corticosteroids.

作者信息

Mohamed Ahmed S, Awwad Ahmad R, Chacko Angel Ann, Dey Shraboni, Braithwaite Brianna, Bhuju Ruchi, Elias Sameh

机构信息

Department of Internal Medicine, Hackensack Meridien Health, Palisades Medical Center, North Bergen, NJ 07047, USA.

Transitional Year Program, Hackensack Meridien Health, Palisades Medical Center, North Bergen, NJ 07047, USA.

出版信息

Curr Oncol. 2025 Mar 10;32(3):156. doi: 10.3390/curroncol32030156.

DOI:10.3390/curroncol32030156
PMID:40136360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11941589/
Abstract

This case report presents a rare occurrence of adrenal insufficiency induced by Zytiga (abiraterone acetate) in a patient with high-risk localized prostatic adenocarcinoma. Abiraterone acetate is a potent, selective and irreversible CYP17A1 inhibitor and is commonly used in the treatment of prostate cancer, but it can cause various endocrine side effects, especially if not used concurrently with the appropriate treatment. The clinical implications of this adverse event and management strategies are discussed here in this case report to raise awareness about this potential risk in patients with prostate cancer undergoing treatment with abiraterone acetate, especially when used in an erroneous manner without monitoring.

摘要

本病例报告展示了在一名高危局限性前列腺癌患者中,泽珂(醋酸阿比特龙)诱发肾上腺功能不全的罕见病例。醋酸阿比特龙是一种强效、选择性且不可逆的CYP17A1抑制剂,常用于治疗前列腺癌,但它会引起各种内分泌副作用,尤其是在未与适当治疗同时使用时。本病例报告讨论了这一不良事件的临床意义及管理策略,以提高正在接受醋酸阿比特龙治疗的前列腺癌患者对这一潜在风险的认识,特别是在错误使用且未进行监测的情况下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aee/11941589/2d9cc051549e/curroncol-32-00156-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aee/11941589/2d9cc051549e/curroncol-32-00156-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aee/11941589/2d9cc051549e/curroncol-32-00156-g001.jpg

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本文引用的文献

1
Abiraterone-Induced Endocrinopathies.阿比特龙诱发的内分泌病。
JCEM Case Rep. 2023 Apr 13;1(2):luad039. doi: 10.1210/jcemcr/luad039. eCollection 2023 Mar.
2
Recognition and Treatment of Adrenal Insufficiency Secondary to Abiraterone: A Case Report and Literature Review.阿比特龙继发肾上腺功能不全的识别与治疗:病例报告及文献复习。
Oncology. 2019;97(5):301-305. doi: 10.1159/000501640. Epub 2019 Aug 7.
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Patient-reported outcomes following abiraterone acetate plus prednisone added to androgen deprivation therapy in patients with newly diagnosed metastatic castration-naive prostate cancer (LATITUDE): an international, randomised phase 3 trial.
新诊断转移性去势敏感性前列腺癌患者中阿比特龙联合泼尼松添加到雄激素剥夺治疗后的患者报告结局(LATITUDE):一项国际性、随机 3 期临床试验。
Lancet Oncol. 2018 Feb;19(2):194-206. doi: 10.1016/S1470-2045(17)30911-7. Epub 2018 Jan 8.
4
Abiraterone plus Prednisone in Metastatic, Castration-Sensitive Prostate Cancer.阿比特龙联合泼尼松治疗转移性去势敏感性前列腺癌。
N Engl J Med. 2017 Jul 27;377(4):352-360. doi: 10.1056/NEJMoa1704174. Epub 2017 Jun 4.
5
Abiraterone in metastatic prostate cancer without previous chemotherapy.阿比特龙治疗既往未接受化疗的转移性前列腺癌。
N Engl J Med. 2013 Jan 10;368(2):138-48. doi: 10.1056/NEJMoa1209096. Epub 2012 Dec 10.
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Abiraterone and increased survival in metastatic prostate cancer.阿比特龙与转移性前列腺癌患者的生存获益
N Engl J Med. 2011 May 26;364(21):1995-2005. doi: 10.1056/NEJMoa1014618.
7
Phase I clinical trial of the CYP17 inhibitor abiraterone acetate demonstrating clinical activity in patients with castration-resistant prostate cancer who received prior ketoconazole therapy.醋酸阿比特龙的 CYP17 抑制剂的 I 期临床试验表明,在接受过酮康唑治疗的去势抵抗性前列腺癌患者中具有临床活性。
J Clin Oncol. 2010 Mar 20;28(9):1481-8. doi: 10.1200/JCO.2009.24.1281. Epub 2010 Feb 16.
8
Selective inhibition of CYP17 with abiraterone acetate is highly active in the treatment of castration-resistant prostate cancer.醋酸阿比特龙对CYP17的选择性抑制在去势抵抗性前列腺癌的治疗中具有高度活性。
J Clin Oncol. 2009 Aug 10;27(23):3742-8. doi: 10.1200/JCO.2008.20.0642. Epub 2009 May 26.
9
CYP17 inhibition as a hormonal strategy for prostate cancer.CYP17抑制作为前列腺癌的一种激素治疗策略。
Nat Clin Pract Urol. 2008 Nov;5(11):610-20. doi: 10.1038/ncpuro1237.
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Br J Cancer. 2004 Jun 14;90(12):2317-25. doi: 10.1038/sj.bjc.6601879.