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本文引用的文献

1
TRK Inhibitors: Clinical Development of Larotrectinib.TRK抑制剂:拉罗替尼的临床开发
Curr Oncol Rep. 2019 Feb 4;21(2):14. doi: 10.1007/s11912-019-0761-y.
2
NTRK fusion-positive cancers and TRK inhibitor therapy.NTRK 融合阳性癌症和 TRK 抑制剂治疗。
Nat Rev Clin Oncol. 2018 Dec;15(12):731-747. doi: 10.1038/s41571-018-0113-0.
3
Inhibiting TRK Proteins in Clinical Cancer Therapy.在临床癌症治疗中抑制TRK蛋白
Cancers (Basel). 2018 Apr 4;10(4):105. doi: 10.3390/cancers10040105.
4
Efficacy of Larotrectinib in TRK Fusion-Positive Cancers in Adults and Children.拉罗替尼在成人和儿童TRK融合阳性癌症中的疗效。
N Engl J Med. 2018 Feb 22;378(8):731-739. doi: 10.1056/NEJMoa1714448.
5
gene fusions as novel targets of cancer therapy across multiple tumour types.基因融合作为多种肿瘤类型癌症治疗的新靶点。
ESMO Open. 2016 Mar 18;1(2):e000023. doi: 10.1136/esmoopen-2015-000023. eCollection 2016.
6
TRKing down an old oncogene in a new era of targeted therapy.在靶向治疗的新时代追踪一个古老的癌基因。
Cancer Discov. 2015 Jan;5(1):25-34. doi: 10.1158/2159-8290.CD-14-0765. Epub 2014 Dec 19.
7
Risk factors for congestive heart failure in US men and women: NHANES I epidemiologic follow-up study.美国男性和女性充血性心力衰竭的危险因素:美国国家健康和营养检查调查I流行病学随访研究
Arch Intern Med. 2001 Apr 9;161(7):996-1002. doi: 10.1001/archinte.161.7.996.

拉罗替尼和恩曲替尼:用于治疗基因融合的儿科和成人患者的TRK抑制剂。

Larotrectinib and Entrectinib: TRK Inhibitors for the Treatment of Pediatric and Adult Patients With Gene Fusion.

作者信息

Dunn Danielle B

机构信息

Houston Methodist Hospital, The Woodlands, Texas.

出版信息

J Adv Pract Oncol. 2020 May-Jun;11(4):418-423. doi: 10.6004/jadpro.2020.11.4.9. Epub 2020 May 1.

DOI:10.6004/jadpro.2020.11.4.9
PMID:33604102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7863124/
Abstract

Two new targeted agents have been approved for pediatric and adult patients with advanced or metastatic solid tumors with neurotrophic receptor tyrosine kinase () gene fusion without an acquired resistance mutation. Larotrectinib and entrectinib are the second and third agents to be approved as tissue agnostic treatments, respectively. gene fusion is now a targetable biomarker for patients who may otherwise be devoid of satisfactory alternative treatment options. In this article, the safety and efficacy trials of each medication, and the initial and ongoing monitoring required for patients on these treatments will be discussed.

摘要

两种新型靶向药物已被批准用于患有晚期或转移性实体瘤且具有神经营养受体酪氨酸激酶()基因融合且无获得性耐药突变的儿科和成年患者。拉罗替尼和恩曲替尼分别是第二种和第三种被批准作为不考虑组织类型的治疗药物。基因融合现在是一种可靶向的生物标志物,适用于那些可能没有令人满意的替代治疗选择的患者。在本文中,将讨论每种药物的安全性和疗效试验,以及接受这些治疗的患者所需的初始和持续监测。