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奥希替尼在携带罕见EGFR L861Q及并发突变的非小细胞肺癌中的疗效:病例报告与文献综述

Efficacy of Osimertinib in NSCLC Harboring Uncommon EGFR L861Q and Concurrent Mutations: Case Report and Literature Review.

作者信息

Lin Ruiting, Chen Ruilian, Chen Zhiqiang, Hu Leihao, Guo Wei, Zhang Zexin, Lin Lizhu, Chen Hanrui

机构信息

First Clinical Medical College, Guangzhou University of Traditional Chinese Medicine, Guangzhou, China.

Department of Oncology, The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine, Guangzhou, China.

出版信息

Front Oncol. 2021 Sep 2;11:731572. doi: 10.3389/fonc.2021.731572. eCollection 2021.

DOI:10.3389/fonc.2021.731572
PMID:34540698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8445031/
Abstract

The efficacy of first-and second-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in NSCLC patients with the EGFR L861Q mutation has been studied previously. However, there is little evidence on the efficacy of osimertinib in NSCLC patients with uncommon mutations. Here, we report the case of a 68-year-old man with advanced NSCLC with concurrent EGFR L861Q mutation as well as TP53 and RB1 mutations. The patient was treated with osimertinib as first-line therapy and achieved a remarkable progression-free survival of 15 months. His symptoms were significantly alleviated and the dose was well tolerated. The findings of the present study indicate that osimertinib might be a good treatment option for NSCLC patients with the L861Q mutation.

摘要

第一代和第二代表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)在伴有EGFR L861Q突变的非小细胞肺癌(NSCLC)患者中的疗效此前已得到研究。然而,关于奥希替尼在伴有罕见突变的NSCLC患者中的疗效,几乎没有证据。在此,我们报告一例68岁患有晚期NSCLC的男性病例,该患者同时存在EGFR L861Q突变以及TP53和RB1突变。该患者接受奥希替尼作为一线治疗,无进展生存期达15个月,效果显著。其症状明显缓解,且对该剂量耐受性良好。本研究结果表明,奥希替尼可能是伴有L861Q突变的NSCLC患者的一个良好治疗选择。

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Efficacy of Osimertinib in NSCLC Harboring Uncommon EGFR L861Q and Concurrent Mutations: Case Report and Literature Review.奥希替尼在携带罕见EGFR L861Q及并发突变的非小细胞肺癌中的疗效:病例报告与文献综述
Front Oncol. 2021 Sep 2;11:731572. doi: 10.3389/fonc.2021.731572. eCollection 2021.
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引用本文的文献

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Inconsistent clinical outcomes following afatinib treatment in NSCLC patients harboring uncommon epidermal growth factor receptor mutation.在携带罕见表皮生长因子受体突变的非小细胞肺癌患者中,阿法替尼治疗后的临床结果不一致。
Front Oncol. 2022 Nov 8;12:999606. doi: 10.3389/fonc.2022.999606. eCollection 2022.

本文引用的文献

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Recent Advances on the Role of EGFR Tyrosine Kinase Inhibitors in the Management of NSCLC With Uncommon, Non Exon 20 Insertions, EGFR Mutations.新型 EGFR 酪氨酸激酶抑制剂在非罕见、非 20 外显子插入 EGFR 突变的 NSCLC 治疗中的作用的最新进展。
J Thorac Oncol. 2021 May;16(5):764-773. doi: 10.1016/j.jtho.2020.12.002. Epub 2020 Dec 14.
2
Circulating tumor DNA in advanced solid tumors: Clinical relevance and future directions.循环肿瘤 DNA 在晚期实体瘤中的临床意义和未来方向。
CA Cancer J Clin. 2021 Mar;71(2):176-190. doi: 10.3322/caac.21650. Epub 2020 Nov 9.
3
Osimertinib, an Irreversible Next-Generation EGFR Tyrosine Kinase Inhibitor, Exerts Antitumor Activity in Various Preclinical NSCLC Models Harboring the Uncommon EGFR Mutations G719X or L861Q or S768I.
奥希替尼是一种不可逆的下一代 EGFR 酪氨酸激酶抑制剂,在携带罕见 EGFR 突变 G719X 或 L861Q 或 S768I 的各种 NSCLC 临床前模型中具有抗肿瘤活性。
Mol Cancer Ther. 2020 Nov;19(11):2298-2307. doi: 10.1158/1535-7163.MCT-20-0103. Epub 2020 Sep 17.
4
Prognostic value of TP53 concurrent mutations for EGFR- TKIs and ALK-TKIs based targeted therapy in advanced non-small cell lung cancer: a meta-analysis.TP53 并发突变对晚期非小细胞肺癌 EGFR-TKIs 和 ALK-TKIs 靶向治疗的预后价值:一项荟萃分析。
BMC Cancer. 2020 Apr 16;20(1):328. doi: 10.1186/s12885-020-06805-5.
5
Concomitant Mutation Confers Worse Prognosis in -Mutated Non-Small Cell Lung Cancer Patients Treated with TKIs.伴随突变使接受酪氨酸激酶抑制剂治疗的EGFR突变非小细胞肺癌患者预后更差。
J Clin Med. 2020 Apr 7;9(4):1047. doi: 10.3390/jcm9041047.
6
Osimertinib for Patients With Non-Small-Cell Lung Cancer Harboring Uncommon EGFR Mutations: A Multicenter, Open-Label, Phase II Trial (KCSG-LU15-09).奥希替尼治疗携带非典型 EGFR 突变的非小细胞肺癌患者:一项多中心、开放标签、II 期试验(KCSG-LU15-09)。
J Clin Oncol. 2020 Feb 10;38(5):488-495. doi: 10.1200/JCO.19.00931. Epub 2019 Dec 11.
7
Concurrent TP53 mutations predict poor outcomes of EGFR-TKI treatments in Chinese patients with advanced NSCLC.同时存在的TP53突变预示着中国晚期非小细胞肺癌患者接受表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗的预后较差。
Cancer Manag Res. 2019 Jun 21;11:5665-5675. doi: 10.2147/CMAR.S201513. eCollection 2019.
8
Concurrent RB1 and TP53 Alterations Define a Subset of EGFR-Mutant Lung Cancers at risk for Histologic Transformation and Inferior Clinical Outcomes.同时存在 RB1 和 TP53 改变的 EGFR 突变型肺癌具有组织学转化和临床结局不良的风险。
J Thorac Oncol. 2019 Oct;14(10):1784-1793. doi: 10.1016/j.jtho.2019.06.002. Epub 2019 Jun 19.
9
Influence of Mutation on Survival in Patients With Advanced -Mutant Non-Small-Cell Lung Cancer.突变对晚期突变型非小细胞肺癌患者生存的影响。
JCO Precis Oncol. 2018;2018. doi: 10.1200/PO.18.00107. Epub 2018 Aug 31.
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Detection of EGFR mutations in plasma circulating tumour DNA as a selection criterion for first-line gefitinib treatment in patients with advanced lung adenocarcinoma (BENEFIT): a phase 2, single-arm, multicentre clinical trial.血浆循环肿瘤 DNA 中 EGFR 突变的检测作为晚期肺腺癌患者一线吉非替尼治疗的选择标准(BENEFIT):一项 2 期、单臂、多中心临床试验。
Lancet Respir Med. 2018 Sep;6(9):681-690. doi: 10.1016/S2213-2600(18)30264-9. Epub 2018 Jul 17.