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本文引用的文献

1
Frontline-matched sibling donor transplant of aplastic anemia patients using primed versus steady-state bone marrow grafts.采用预激与稳态骨髓移植物的再生障碍性贫血患者一线匹配同胞供体移植。
Ann Hematol. 2022 Feb;101(2):421-428. doi: 10.1007/s00277-021-04708-4. Epub 2021 Oct 31.
2
Androgen derivatives improve blood counts and elongate telomere length in adult cryptic dyskeratosis congenita.雄激素衍生物可改善血细胞计数并延长成人隐匿性先天性角化不良症患者的端粒长度。
Br J Haematol. 2021 May;193(3):669-673. doi: 10.1111/bjh.16997. Epub 2020 Aug 3.
3
Androgens and Anemia: Current Trends and Future Prospects.雄激素与贫血:当前趋势与未来展望。
Front Endocrinol (Lausanne). 2019 Nov 14;10:754. doi: 10.3389/fendo.2019.00754. eCollection 2019.
4
Outcomes of paroxysmal nocturnal hemoglobinuria in the pediatric age group in a resource-constrained setting.资源有限环境下儿科阵发性睡眠性血红蛋白尿症的结局。
Pediatr Blood Cancer. 2020 Apr;67(4):e27712. doi: 10.1002/pbc.27712. Epub 2019 Mar 26.
5
Aplastic Anemia.再生障碍性贫血
N Engl J Med. 2018 Oct 25;379(17):1643-1656. doi: 10.1056/NEJMra1413485.
6
Similar telomere attrition rates in androgen-treated and untreated patients with dyskeratosis congenita.先天性角化不良患者经雄激素治疗和未经治疗者的端粒损耗速率相似。
Blood Adv. 2018 Jun 12;2(11):1243-1249. doi: 10.1182/bloodadvances.2018016964.
7
Treatment of inherited bone marrow failure syndromes beyond transplantation.骨髓衰竭综合征的移植治疗以外。
Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):96-101. doi: 10.1182/asheducation-2017.1.96.
8
Danazol Treatment for Telomere Diseases.达那唑治疗端粒疾病
N Engl J Med. 2016 May 19;374(20):1922-31. doi: 10.1056/NEJMoa1515319.
9
Androgen therapy in Fanconi anemia: A retrospective analysis of 30 years in Germany.范可尼贫血的雄激素治疗:德国30年回顾性分析
Pediatr Hematol Oncol. 2016 Feb;33(1):5-12. doi: 10.3109/08880018.2015.1129567. Epub 2016 Feb 22.
10
Therapeutic effect of androgen therapy in a mouse model of aplastic anemia produced by short telomeres.雄激素疗法对短端粒所致再生障碍性贫血小鼠模型的治疗效果。
Haematologica. 2015 Oct;100(10):1267-74. doi: 10.3324/haematol.2015.129239. Epub 2015 Jul 23.

雄激素疗法在获得性再生障碍性贫血及其他骨髓衰竭综合征中的作用。

The role of androgen therapy in acquired aplastic anemia and other bone marrow failure syndromes.

作者信息

Nassani Momen, Fakih Riad El, Passweg Jakob, Cesaro Simone, Alzahrani Hazzaa, Alahmari Ali, Bonfim Carmem, Iftikhar Raheel, Albeihany Amal, Halkes Constantijn, Ahmed Syed Osman, Dufour Carlo, Aljurf Mahmoud

机构信息

Department of Hematology, Stem Cell Transplant & Cellular Therapy, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

Department of Hematology, University Hospital Basel, Basel, Switzerland.

出版信息

Front Oncol. 2023 May 8;13:1135160. doi: 10.3389/fonc.2023.1135160. eCollection 2023.

DOI:10.3389/fonc.2023.1135160
PMID:37223686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10200973/
Abstract

Bone marrow failure syndromes are a heterogeneous group of diseases. With the major advancements in diagnostic tools and sequencing techniques, these diseases may be better classified and therapies may be further tailored. Androgens, a historic group of drugs, were found to stimulate hematopoiesis by enhancing the responsiveness of progenitors. These agents have been used for decades to treat different forms of bone marrow failure. With the availability of more effective pathways to treat BMF, androgens are less used currently. Nevertheless, this group of drugs may serve BMF patients where standard therapy is contraindicated or not available. In this article, we review the published literature addressing the use of androgens in BMF patients and we make recommendations on how to best use this class of drugs within the current therapeutic landscape.

摘要

骨髓衰竭综合征是一组异质性疾病。随着诊断工具和测序技术的重大进展,这些疾病可能会得到更好的分类,治疗方法也可能会进一步优化。雄激素是一类历史悠久的药物,被发现可通过增强祖细胞的反应性来刺激造血。这些药物已被用于治疗不同形式的骨髓衰竭数十年。随着治疗骨髓衰竭更有效途径的出现,目前雄激素的使用较少。然而,在标准治疗禁忌或不可用时,这类药物可能对骨髓衰竭患者有用。在本文中,我们回顾了已发表的关于雄激素在骨髓衰竭患者中应用的文献,并就如何在当前治疗格局中最佳使用这类药物提出建议。