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恩曲替尼诱发的神经性关节病:病例报告

Development of Neuropathic Arthropathy With Entrectinib: Case Report.

作者信息

Giustini Nicholas P, Oh Hanna, Eaton Keith D

机构信息

Division of Hematology, Department of Medicine, University of Washington, Seattle, Washington.

Department of Rehabilitation Medicine, University of Washington, Seattle, Washington.

出版信息

JTO Clin Res Rep. 2022 Sep 30;3(11):100419. doi: 10.1016/j.jtocrr.2022.100419. eCollection 2022 Nov.

DOI:10.1016/j.jtocrr.2022.100419
PMID:36340796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9634017/
Abstract

TRK inhibition can lead to on-target neurologic adverse events. Two cases illustrate the development of neuropathic arthropathy as a side effect of entrectinib. After starting entrectinib, both patients developed foot pain, swelling, and sensory changes with magnetic resonance imaging revealing marrow edema. Providers should have a low threshold to investigate foot pain or gait abnormalities thoroughly with magnetic resonance imaging and referral to specialists to aid in the diagnosis of neuropathic arthropathy, with consideration to transition to an alternative agent.

摘要

TRK抑制可导致靶向性神经系统不良事件。两例病例说明了神经关节病作为恩曲替尼副作用的发生情况。开始使用恩曲替尼后,两名患者均出现足部疼痛、肿胀和感觉改变,磁共振成像显示骨髓水肿。医疗人员对于彻底调查足部疼痛或步态异常应保持较低阈值,通过磁共振成像并转诊至专科医生以协助诊断神经关节病,并考虑换用其他药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ea6/9634017/8ea9c8d7c589/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ea6/9634017/33d1faf083f1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ea6/9634017/8ea9c8d7c589/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ea6/9634017/33d1faf083f1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ea6/9634017/8ea9c8d7c589/gr2.jpg

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The European Medicines Agency review of entrectinib for the treatment of adult or paediatric patients with solid tumours who have a neurotrophic tyrosine receptor kinase gene fusions and adult patients with non-small-cell lung cancer harbouring ROS1 rearrangements.欧洲药品管理局对恩曲替尼用于治疗患有神经营养性酪氨酸受体激酶基因融合的成年或儿科实体瘤患者以及患有ROS1重排的非小细胞肺癌成年患者的审查。
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Tropomyosin receptor kinase (TRK) biology and the role of NTRK gene fusions in cancer.原肌球蛋白受体激酶(TRK)生物学和 NTRK 基因融合在癌症中的作用。
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Recurrent and novel mutations in the NTRK1 gene lead to rare congenital insensitivity to pain with anhidrosis in two Chinese patients.
NTRK1基因中的复发性和新突变导致两名中国患者出现罕见的先天性无痛觉伴无汗症。
Clin Chim Acta. 2017 May;468:39-45. doi: 10.1016/j.cca.2017.02.007. Epub 2017 Feb 10.
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The Charcot foot: pathophysiology, diagnosis and classification.夏科氏足:病理生理学、诊断与分类
Bone Joint J. 2016 Sep;98-B(9):1155-9. doi: 10.1302/0301-620X.98B9.37038.