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MicroRNA-34c-3p target inhibiting NOTCH1 suppresses chemosensitivity and metastasis of non-small cell lung cancer.微小 RNA-34c-3p 靶向抑制 NOTCH1 抑制非小细胞肺癌的化疗敏感性和转移。
J Int Med Res. 2020 Mar;48(3):300060520904847. doi: 10.1177/0300060520904847.
2
Mechanism, safety and efficacy of three tyrosine kinase inhibitors lapatinib, neratinib and pyrotinib in HER2-positive breast cancer.三种酪氨酸激酶抑制剂拉帕替尼、奈拉替尼和吡咯替尼在HER2阳性乳腺癌中的作用机制、安全性及疗效
Am J Cancer Res. 2019 Oct 1;9(10):2103-2119. eCollection 2019.
3
Pan-Cancer Landscape and Analysis of ERBB2 Mutations Identifies Poziotinib as a Clinically Active Inhibitor and Enhancer of T-DM1 Activity.泛癌种全景分析和 ERBB2 突变鉴定表明波齐替尼是一种具有临床活性的抑制剂,可增强 T-DM1 的活性。
Cancer Cell. 2019 Oct 14;36(4):444-457.e7. doi: 10.1016/j.ccell.2019.09.001. Epub 2019 Oct 3.
4
HER2-targeted therapies - a role beyond breast cancer.曲妥珠单抗等 HER2 靶向治疗——超越乳腺癌的应用。
Nat Rev Clin Oncol. 2020 Jan;17(1):33-48. doi: 10.1038/s41571-019-0268-3. Epub 2019 Sep 23.
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Role of KEAP1/NFE2L2 Mutations in the Chemotherapeutic Response of Patients with Non-Small Cell Lung Cancer.KEAP1/NFE2L2 突变在非小细胞肺癌患者化疗反应中的作用。
Clin Cancer Res. 2020 Jan 1;26(1):274-281. doi: 10.1158/1078-0432.CCR-19-1237. Epub 2019 Sep 23.
6
Pyrotinib versus lapatinib in HER2-positive breast cancer.吡咯替尼与拉帕替尼治疗HER2阳性乳腺癌的对比
Lancet Oncol. 2019 Oct;20(10):e562. doi: 10.1016/S1470-2045(19)30568-6. Epub 2019 Aug 30.
7
Pyrotinib or Lapatinib Combined With Capecitabine in HER2-Positive Metastatic Breast Cancer With Prior Taxanes, Anthracyclines, and/or Trastuzumab: A Randomized, Phase II Study.吡咯替尼或拉帕替尼联合卡培他滨治疗既往接受紫杉类、蒽环类和/或曲妥珠单抗治疗的 HER2 阳性转移性乳腺癌:一项随机、Ⅱ期研究。
J Clin Oncol. 2019 Oct 10;37(29):2610-2619. doi: 10.1200/JCO.19.00108. Epub 2019 Aug 20.
8
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。
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Lung Cancer. 2019 Aug;134:42-45. doi: 10.1016/j.lungcan.2019.05.002. Epub 2019 May 3.
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HER2 exon 20 insertions in non-small-cell lung cancer are sensitive to the irreversible pan-HER receptor tyrosine kinase inhibitor pyrotinib.非小细胞肺癌中的 HER2 外显子 20 插入对不可逆的泛 HER 受体酪氨酸激酶抑制剂吡咯替尼敏感。
Ann Oncol. 2019 Mar 1;30(3):447-455. doi: 10.1093/annonc/mdy542.

人表皮生长因子受体2(HER2)扩增的转移性肺腺癌对四线吡咯替尼治疗有反应:一例病例报告

HER2-amplified metastatic lung adenocarcinoma responds to fourth-line pyrotinib therapy: A case report.

作者信息

Gong Kan, Yang Yi, Huang Huan, Kuang Xunjie, Yang Xueqin

机构信息

Cancer Center, Daping Hospital, Army Medical University, Chongqing 400042, P.R. China.

出版信息

Mol Clin Oncol. 2021 Oct;15(4):213. doi: 10.3892/mco.2021.2375. Epub 2021 Aug 19.

DOI:10.3892/mco.2021.2375
PMID:34476097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8408680/
Abstract

Despite the success of anti-HER2 therapy in patients with breast cancer with HER2 amplification or HER2 overexpression, the results of clinical trials on anti-HER2 therapy for lung cancer have not been satisfactory. The aim of the present study was to report a case of a non-smoker, female patient diagnosed with stage IIIA lung adenocarcinoma harboring amplification. The disease progressed despite surgery and multiple lines of chemotherapy, plus trastuzumab or lapatinib. The pan-ErbB inhibitor pyrotinib (400 mg/day) was commenced as a fourth-line regimen, and the patient achieved complete response with a time to progression (TTP) of 6 months. After the lung adenocarcinoma progressed, pyrotinib was continued, along with anlotinib and nivolumab. The patient achieved stable disease (SD) status with another 6 months of TTP. The overall survival of the patient was 28 months. Therefore, the present case suggests that the development of novel drugs may provide new and effective therapeutic regimens for lung cancer with HER2 amplification.

摘要

尽管抗HER2疗法在HER2扩增或HER2过表达的乳腺癌患者中取得了成功,但抗HER2疗法用于肺癌的临床试验结果并不令人满意。本研究的目的是报告一例非吸烟女性患者,诊断为ⅢA期肺腺癌且伴有HER2扩增。尽管接受了手术、多线化疗以及曲妥珠单抗或拉帕替尼治疗,疾病仍进展。作为四线治疗方案开始使用泛ErbB抑制剂吡咯替尼(400毫克/天),患者获得完全缓解,疾病进展时间(TTP)为6个月。肺腺癌进展后,继续使用吡咯替尼,同时联合安罗替尼和纳武单抗。患者达到疾病稳定(SD)状态,TTP又持续了6个月。患者的总生存期为28个月。因此,本病例表明新药的研发可能为HER2扩增的肺癌提供新的有效治疗方案。