Dunn Danielle B
Houston Methodist Hospital, The Woodlands, Texas.
J Adv Pract Oncol. 2020 May-Jun;11(4):418-423. doi: 10.6004/jadpro.2020.11.4.9. Epub 2020 May 1.
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.
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。