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吉瑞替尼诱发的垂体功能减退:一例报告

Gilteritinib-Induced Hypopituitarism: A Case Report.

作者信息

Hori Yuri, Okada Yosuke, Sonoda Satomi, Torimoto Keiichi, Tanaka Yoshiya

机构信息

Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, JPN.

出版信息

Cureus. 2024 Sep 28;16(9):e70401. doi: 10.7759/cureus.70401. eCollection 2024 Sep.

DOI:10.7759/cureus.70401
PMID:39473682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11518918/
Abstract

Gilteritinib is a tyrosine kinase inhibitor (TKI) that treats acute myeloid leukemia (AML) by inhibiting FMS-like tyrosine kinase 3 (FLT3). This is a report on hypopituitarism induced by gilteritinib and its resolution following withdrawal. A 54-year-old woman was treated with gilteritinib for AML. She subsequently developed general fatigue. Blood tests showed low levels of anterior pituitary hormone. After 10 months of gilteritinib withdrawal, the levels of anterior pituitary hormones returned to normal values. When nonspecific symptoms such as fatigue in patients treated with gilteritinib are coupled with electrolyte abnormalities, a close checkup for hypopituitarism is recommended.

摘要

吉瑞替尼是一种酪氨酸激酶抑制剂(TKI),通过抑制FMS样酪氨酸激酶3(FLT3)来治疗急性髓系白血病(AML)。本文报告了吉瑞替尼诱发的垂体功能减退及其停药后的恢复情况。一名54岁女性因AML接受吉瑞替尼治疗。随后她出现全身乏力。血液检查显示垂体前叶激素水平较低。停用吉瑞替尼10个月后,垂体前叶激素水平恢复至正常范围。当接受吉瑞替尼治疗的患者出现乏力等非特异性症状并伴有电解质异常时,建议密切检查是否存在垂体功能减退。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf73/11518918/b884b9a10871/cureus-0016-00000070401-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf73/11518918/d82ccc72c5b7/cureus-0016-00000070401-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf73/11518918/b884b9a10871/cureus-0016-00000070401-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf73/11518918/d82ccc72c5b7/cureus-0016-00000070401-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf73/11518918/b884b9a10871/cureus-0016-00000070401-i02.jpg

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本文引用的文献

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Follow-up of patients with R/R FLT3-mutation-positive AML treated with gilteritinib in the phase 3 ADMIRAL trial.在3期ADMIRAL试验中接受吉列替尼治疗的复发/难治性FLT3突变阳性急性髓系白血病患者的随访
Blood. 2022 Jun 9;139(23):3366-3375. doi: 10.1182/blood.2021011583.
2
FDA Approval Summary: Gilteritinib for Relapsed or Refractory Acute Myeloid Leukemia with a Mutation.FDA 批准概要:吉特替尼用于伴有突变的复发/难治性急性髓系白血病。
Clin Cancer Res. 2021 Jul 1;27(13):3515-3521. doi: 10.1158/1078-0432.CCR-20-4271. Epub 2021 Feb 25.
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[Pharmacological and clinical profile of gilteritinib (Xospata tablets 40 mg), a therapeutic agent for relapsed or refractory FLT3-mutated acute myeloid leukemia].
吉瑞替尼(Xospata片剂,40毫克)的药理及临床概况,一种用于复发或难治性FLT3突变急性髓系白血病的治疗药物
Nihon Yakurigaku Zasshi. 2021;156(1):37-46. doi: 10.1254/fpj.20050.
4
Gilteritinib or Chemotherapy for Relapsed or Refractory -Mutated AML.吉特替尼与化疗用于治疗复发/难治性 - 突变型 AML。
N Engl J Med. 2019 Oct 31;381(18):1728-1740. doi: 10.1056/NEJMoa1902688.
5
Lapatinib decreases the ACTH production and proliferation of corticotroph tumor cells.拉帕替尼可降低促肾上腺皮质激素的产生和促肾上腺皮质细胞瘤细胞的增殖。
Endocr J. 2019 Jun 28;66(6):515-522. doi: 10.1507/endocrj.EJ18-0491. Epub 2019 Mar 15.
6
Gilteritinib, a FLT3/AXL inhibitor, shows antileukemic activity in mouse models of FLT3 mutated acute myeloid leukemia.吉特替尼,一种 FLT3/AXL 抑制剂,在 FLT3 突变型急性髓系白血病的小鼠模型中显示出抗白血病活性。
Invest New Drugs. 2017 Oct;35(5):556-565. doi: 10.1007/s10637-017-0470-z. Epub 2017 May 17.
7
Endocrine side effects of broad-acting kinase inhibitors.广泛作用激酶抑制剂的内分泌副作用。
Endocr Relat Cancer. 2010 Aug 16;17(3):R233-44. doi: 10.1677/ERC-10-0082. Print 2010 Sep.
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G-protein-coupled receptors and tyrosine kinases: crossroads in cell signaling and regulation.G蛋白偶联受体与酪氨酸激酶:细胞信号传导与调控的交汇点
Trends Endocrinol Metab. 2006 Mar;17(2):48-54. doi: 10.1016/j.tem.2006.01.006. Epub 2006 Feb 7.