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本文引用的文献

1
Impact of TP53 mutation status on systemic treatment outcome in ALK-rearranged non-small-cell lung cancer.TP53 突变状态对 ALK 重排非小细胞肺癌系统治疗结局的影响。
Ann Oncol. 2018 Oct 1;29(10):2068-2075. doi: 10.1093/annonc/mdy333.
2
-rearrangement neuroendocrine carcinoma of the lung: a comprehensive study of a rare case series and review of literature.肺重排神经内分泌癌:罕见病例系列的综合研究及文献综述
Onco Targets Ther. 2018 Aug 17;11:4991-4998. doi: 10.2147/OTT.S172124. eCollection 2018.
3
mutations predict for poor survival in rearrangement lung adenocarcinoma patients treated with crizotinib.在接受克唑替尼治疗的重排型肺腺癌患者中,突变预示着较差的生存率。
J Thorac Dis. 2018 May;10(5):2991-2998. doi: 10.21037/jtd.2018.04.98.
4
Sequential ALK Inhibitors Can Select for Lorlatinib-Resistant Compound Mutations in ALK-Positive Lung Cancer.序贯 ALK 抑制剂可选择 ALK 阳性肺癌中 lorlatinib 耐药的复合突变。
Cancer Discov. 2018 Jun;8(6):714-729. doi: 10.1158/2159-8290.CD-17-1256. Epub 2018 Apr 12.
5
Detection of known and novel ALK fusion transcripts in lung cancer patients using next-generation sequencing approaches.采用下一代测序方法检测肺癌患者中的已知和新型 ALK 融合转录本。
Sci Rep. 2017 Oct 2;7(1):12510. doi: 10.1038/s41598-017-12679-8.
6
ALK in Non-Small Cell Lung Cancer (NSCLC) Pathobiology, Epidemiology, Detection from Tumor Tissue and Algorithm Diagnosis in a Daily Practice.间变性淋巴瘤激酶在非小细胞肺癌中的病理生物学、流行病学、肿瘤组织检测及日常实践中的算法诊断
Cancers (Basel). 2017 Aug 12;9(8):107. doi: 10.3390/cancers9080107.
7
Pooled Systemic Efficacy and Safety Data from the Pivotal Phase II Studies (NP28673 and NP28761) of Alectinib in ALK-positive Non-Small Cell Lung Cancer.阿来替尼治疗 ALK 阳性非小细胞肺癌的关键性 II 期研究(NP28673 和 NP28761)的汇总全身疗效和安全性数据。
J Thorac Oncol. 2017 Oct;12(10):1552-1560. doi: 10.1016/j.jtho.2017.06.070. Epub 2017 Jul 6.
8
Ceritinib versus chemotherapy in patients with ALK-rearranged non-small-cell lung cancer previously given chemotherapy and crizotinib (ASCEND-5): a randomised, controlled, open-label, phase 3 trial.塞瑞替尼与化疗用于既往接受过化疗和克唑替尼治疗的间变性淋巴瘤激酶(ALK)重排的非小细胞肺癌患者(ASCEND-5):一项随机、对照、开放标签、III 期临床试验。
Lancet Oncol. 2017 Jul;18(7):874-886. doi: 10.1016/S1470-2045(17)30339-X. Epub 2017 Jun 9.
9
A Case of Metastatic Atypical Neuroendocrine Tumor with Translocation and Diffuse Brain Metastases.一例伴有易位和弥漫性脑转移的转移性非典型神经内分泌肿瘤病例。
Oncologist. 2017 Jul;22(7):768-773. doi: 10.1634/theoncologist.2017-0054. Epub 2017 May 15.
10
Multiple Acquired Resistance Mutations of the ALK Tyrosine Kinase Domain after Sequential Use of ALK Inhibitors.序贯使用ALK抑制剂后ALK酪氨酸激酶结构域的多重获得性耐药突变
J Thorac Oncol. 2017 May;12(5):e49-e51. doi: 10.1016/j.jtho.2017.01.009.

肺原发性非典型类癌伴 EML4-ALK 重排 1 例。

A case of primary pulmonary atypical carcinoid with EML4-ALK rearrangement.

机构信息

Department of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, People's Republic of China.

出版信息

Cancer Biol Ther. 2020;21(1):12-16. doi: 10.1080/15384047.2019.1665957. Epub 2019 Sep 27.

DOI:10.1080/15384047.2019.1665957
PMID:31559892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7012075/
Abstract

Targeted therapy has revolutionized the treatment pattern of advanced drive gene mutation positive non-small cell lung cancer (NSCLC). Advanced testing techniques enable physicians to detect these gene alterations in the clinic, thereby offering targeted therapies as treatment options to their patients. In this article, we reported a 52-year-old Chinese female with a pulmonary nodule in her left lower lung. After thoracoscopic lobectomy, a histopathological diagnosis of moderately differentiated atypical carcinoid (AC) was made. Anaplastic lymphoma kinase (ALK) rearrangement was detected, which is a rare phenomenon in AC. After the failure of chemotherapy and radiotherapy, the patient started taking crizotinib, subsequently with ceritinib, and then alectinib. This sequential therapy approach has significant clinical benefits for the patient. This article reviewed the clinical significance and drug resistance mechanism of ALK rearrangement in lung cancer. We also discussed recent and ongoing researches and applications of ALK-tyrosine kinase inhibitors (ALK-TKIs).

摘要

靶向治疗已经彻底改变了晚期驱动基因阳性非小细胞肺癌(NSCLC)的治疗模式。先进的检测技术使医生能够在临床中检测到这些基因改变,从而为患者提供靶向治疗作为治疗选择。在本文中,我们报告了一名 52 岁的中国女性,她的左下肺有一个肺结节。在胸腔镜肺叶切除术后,组织病理学诊断为中分化非典型类癌(AC)。检测到间变性淋巴瘤激酶(ALK)重排,这在 AC 中较为罕见。在化疗和放疗失败后,患者开始服用克唑替尼,随后是塞瑞替尼,然后是阿来替尼。这种序贯治疗方法对患者具有显著的临床获益。本文综述了肺癌中 ALK 重排的临床意义和耐药机制。我们还讨论了 ALK-酪氨酸激酶抑制剂(ALK-TKIs)的最新研究进展和应用。