摘要
简介:一些报告证明了通过饲管或经皮内镜胃造口术(PEG)给予激酶抑制剂的可行性和有利结果,主要是在暴露于第一代化合物的非小细胞肺癌(NSCLC)患者中。在这里,我们提出了ALK阳性NSCLC患者的情况,该患者通过鼻胃管(NGT)给予ceritinib(一种新型ALK抑制剂)实现脑和颅外疾病反应。此外,我们提供了一项综述,收集通过NGT或PEG摄入靶向药物获得的临床成功。 病例报告:一名53岁的从不吸烟女性被诊断出患有ALK重排的IV期肺腺癌。在对克唑替尼和几种全身治疗作出明显反应后,鉴于胸膜 - 食管瘘的发展,需要用于治疗ceritinib的NGT定位。肠内给药可以显着减少肝脏和脑部疾病的定位。 文献综述和讨论:通过NGT或PEG给药的大多数激酶抑制剂可用于EGFR突变(7)或ALK阳性(7种,包括我们的报告)NSCLC患者。描述了另外五个涉及不同恶性肿瘤的病例。肠内给药主要是与疾病相关的呼吸障碍所需要的,需要在紧急情况下进行机械通气。在我们的病例中,肠内注射ceritinib获得的大脑和颅外反应表明,在这些情况下,新型抑制剂的提出可能发生在第一代化合物失败后甚至是前期。实际上,当需要快速的全身和脑内疾病反应时,它们对脑转移的更大效力和活性也指出了它们在一线治疗中的肠内给药的作用。
关键词: 非小细胞肺癌,ALK重排,ceritinib,激酶抑制剂,肠内给药,鼻胃管。
图形摘要
Current Drug Targets
Title:Enteral Administration of TKIs: Report of a Response to Ceritinib in an ALK-positive NSCLC Patient and Literature Review
Volume: 19 Issue: 14
关键词: 非小细胞肺癌,ALK重排,ceritinib,激酶抑制剂,肠内给药,鼻胃管。
摘要: Introduction: Several reports attest the feasibility and the favorable outcomes of kinase inhibitors administration through feeding tubes or Percutaneous Endoscopic Gastrostomies (PEG), mainly in Non-Small Cell Lung Cancer (NSCLC) patients exposed to first-generation compounds. Here we present the case of an ALK-positive NSCLC patient who achieved cerebral and extra-cranial disease response with ceritinib (a novel ALK inhibitor) administered through a Nasogastric Tube (NGT). We moreover provide a review gathering clinical successes obtained with targeted agents intake through NGT or PEG.
Case Presentation: A 53-year-old never-smoker woman was diagnosed with ALK-rearranged stage IV lung adenocarcinoma. After a brilliant response to crizotinib and several lines of systemic therapy, NGT positioning intended for ceritinib administration was required, given the development of a pleuro-esophageal fistula. Enteral drug administration allowed a significant reduction of hepatic and cerebral disease localizations.
Literature review and discussion: The majority of kinase inhibitors administration through NGT or PEG accounts for EGFR-mutated (seven) or ALK-positive (seven, including our report) NSCLC patients. Five additional cases concerning different malignancies were described. Enteral drug administration was mostly required by disease-related respiratory impairment, requiring mechanical ventilation in the emergency setting. In our case, the cerebral and extra-cranial response obtained with enteral ceritinib intake suggests the proposition of novel inhibitors in these circumstances may take place after first-generation compounds failure or even upfront. Indeed, their grater potency and activity against brain metastases point out the role of their enteral administration in the first-line setting too, when a rapid systemic and intra-cerebral disease response is required.
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Cite this article as:
Enteral Administration of TKIs: Report of a Response to Ceritinib in an ALK-positive NSCLC Patient and Literature Review, Current Drug Targets 2018; 19 (14) . https://dx.doi.org/10.2174/1389450119666180213102939
DOI https://dx.doi.org/10.2174/1389450119666180213102939 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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