• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

病例报告:奥希替尼诱发的急性间质性肺病。

Case Report: Osimertinib-induced acute interstitial lung disease.

作者信息

Lin Zhiwu, Wu Liang, Yu Yang, Jiang Jiudong, Yang Yanchun, Xiao Guibao

机构信息

Department of Thoracic Surgery, Ziyang Central Hospital, Ziyang, China.

Department of Infectious Diseases, Ziyang Central Hospital, Ziyang, China.

出版信息

Front Pharmacol. 2025 Jun 5;16:1608733. doi: 10.3389/fphar.2025.1608733. eCollection 2025.

DOI:10.3389/fphar.2025.1608733
PMID:40538542
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12176793/
Abstract

Osimertinib is a third-generation irreversible epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) that selectively targets EGFR-TKI-sensitive mutations, thereby inhibiting tumor cell proliferation, migration, and invasion. Herein, we present a case of osimertinib-induced interstitial lung disease (ILD) in an 80-year-old woman with EGFR-mutated lung adenocarcinoma. The patient was treated with osimertinib as first-line therapy for metastatic non-small cell lung cancer (NSCLC). On day 45 of treatment, she experienced acute onset of severe dyspnea, which rapidly progressed to diffuse bilateral pulmonary consolidation and profound hypoxemia. Despite discontinuation of osimertinib and administration of aggressive supportive care, her clinical condition continued to deteriorate, ultimately resulting in a fatal outcome. This case underscores the importance of monitoring respiratory symptoms in patients receiving EGFR-TKIs, promptly diagnosing ILD, and implementing early intervention to mitigate adverse outcomes.

摘要

奥希替尼是一种第三代不可逆表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI),它选择性地靶向EGFR-TKI敏感突变,从而抑制肿瘤细胞增殖、迁移和侵袭。在此,我们报告一例80岁患有EGFR突变肺腺癌的女性患者发生奥希替尼诱导的间质性肺病(ILD)的病例。该患者接受奥希替尼作为转移性非小细胞肺癌(NSCLC)的一线治疗。在治疗的第45天,她突然出现严重呼吸困难,迅速发展为双侧肺部弥漫性实变和严重低氧血症。尽管停用了奥希替尼并给予积极的支持治疗,她的临床状况仍持续恶化,最终导致死亡。该病例强调了在接受EGFR-TKIs治疗的患者中监测呼吸道症状、及时诊断ILD以及实施早期干预以减轻不良后果的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd19/12176793/e664df3b2c94/fphar-16-1608733-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd19/12176793/92b37c219631/fphar-16-1608733-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd19/12176793/d6dec7274532/fphar-16-1608733-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd19/12176793/e664df3b2c94/fphar-16-1608733-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd19/12176793/92b37c219631/fphar-16-1608733-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd19/12176793/d6dec7274532/fphar-16-1608733-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd19/12176793/e664df3b2c94/fphar-16-1608733-g003.jpg

相似文献

1
Case Report: Osimertinib-induced acute interstitial lung disease.病例报告:奥希替尼诱发的急性间质性肺病。
Front Pharmacol. 2025 Jun 5;16:1608733. doi: 10.3389/fphar.2025.1608733. eCollection 2025.
2
Adjuvant epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) for the treatment of people with resected stage I to III non-small-cell lung cancer and EGFR mutation.辅助性表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKIs)用于治疗已切除的Ⅰ至Ⅲ期非小细胞肺癌且伴有EGFR突变的患者。
Cochrane Database Syst Rev. 2025 May 27;5(5):CD015140. doi: 10.1002/14651858.CD015140.pub2.
3
Front-line therapy for brain metastases and non-brain metastases in advanced epidermal growth factor receptor-mutated non-small cell lung cancer: a network meta-analysis.晚期表皮生长因子受体突变型非小细胞肺癌脑转移和非脑转移的一线治疗:一项网络荟萃分析。
Chin Med J (Engl). 2023 Nov 5;136(21):2551-2561. doi: 10.1097/CM9.0000000000002468.
4
What is the optimal first-line regimen for advanced non-small cell lung cancer patients with epidermal growth factor receptor mutation: a systematic review and network meta-analysis.表皮生长因子受体突变的晚期非小细胞肺癌患者的最佳一线治疗方案是什么:一项系统评价和网状Meta分析
BMC Pulm Med. 2024 Dec 18;24(1):620. doi: 10.1186/s12890-024-03438-3.
5
A Multicenter Open-Label Randomized Phase II Study of Osimertinib With and Without Ramucirumab in Tyrosine Kinase Inhibitor-Naïve -Mutant Metastatic Non-Small Cell Lung Cancer (RAMOSE trial).一项关于奥希替尼联合或不联合雷莫西尤单抗用于酪氨酸激酶抑制剂初治的EGFR突变转移性非小细胞肺癌的多中心开放标签随机II期研究(RAMOSE试验)。
J Clin Oncol. 2025 Feb;43(4):403-411. doi: 10.1200/JCO.24.00533. Epub 2024 Oct 8.
6
EGFR-TKIs or EGFR-TKIs combination treatments for untreated advanced EGFR-mutated NSCLC: a network meta-analysis.未经治疗的晚期 EGFR 突变型 NSCLC 的 EGFR-TKIs 或 EGFR-TKIs 联合治疗:一项网络荟萃分析。
BMC Cancer. 2024 Nov 12;24(1):1390. doi: 10.1186/s12885-024-13168-8.
7
First-Line Osimertinib for Previously Untreated Patients With NSCLC and Uncommon EGFR Mutations: The UNICORN Phase 2 Nonrandomized Clinical Trial.未经治 NSCLC 患者中常见 EGFR 突变的一线奥希替尼治疗:UNICORN 期 2 非随机临床试验。
JAMA Oncol. 2024 Jan 1;10(1):43-51. doi: 10.1001/jamaoncol.2023.5013.
8
Case report: EGFR-TKI rechallenge after osimertinib-induced interstitial lung disease: a case report and literature review.病例报告:奥希替尼诱发间质性肺疾病后重新使用表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI):一例病例报告及文献综述
Front Pharmacol. 2024 Jun 4;15:1410684. doi: 10.3389/fphar.2024.1410684. eCollection 2024.
9
Risk Factors Associated with Suboptimal Real-World Outcomes in Patients with EGFR-Mutated Non-Small Cell Lung Cancer Treated with Front-Line Recommended Therapy.表皮生长因子受体(EGFR)突变的非小细胞肺癌患者接受一线推荐治疗后,与欠佳的真实世界治疗结果相关的风险因素
Adv Ther. 2025 May 29. doi: 10.1007/s12325-025-03234-3.
10
Efficacy and safety of immune checkpoint inhibitors for individuals with advanced EGFR-mutated non-small-cell lung cancer who progressed on EGFR tyrosine-kinase inhibitors: a systematic review, meta-analysis, and network meta-analysis.免疫检查点抑制剂在 EGFR 酪氨酸激酶抑制剂治疗进展后的晚期 EGFR 突变型非小细胞肺癌患者中的疗效和安全性:系统评价、荟萃分析和网络荟萃分析。
Lancet Oncol. 2024 Oct;25(10):1347-1356. doi: 10.1016/S1470-2045(24)00379-6. Epub 2024 Aug 16.

本文引用的文献

1
Adverse Event Profile of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors for Non-small Cell Lung Cancer: An Updated Meta-analysis.表皮生长因子受体酪氨酸激酶抑制剂治疗非小细胞肺癌的不良反应谱:一项更新的荟萃分析。
Target Oncol. 2024 Jul;19(4):547-564. doi: 10.1007/s11523-024-01073-w. Epub 2024 Jun 1.
2
Quantification of BIM mRNA in circulating tumor cells of osimertinib-treated patients with EGFR mutation-positive lung cancer.奥希替尼治疗的 EGFR 突变阳性肺癌患者循环肿瘤细胞中 BIM mRNA 的定量分析。
Respir Investig. 2021 Jul;59(4):535-544. doi: 10.1016/j.resinv.2021.03.010. Epub 2021 Apr 29.
3
Molecular and Clinical Features of EGFR-TKI-Associated Lung Injury.
表皮生长因子受体酪氨酸激酶抑制剂相关肺损伤的分子和临床特征。
Int J Mol Sci. 2021 Jan 14;22(2):792. doi: 10.3390/ijms22020792.
4
Identification of key genes and biological pathways in lung adenocarcinoma via bioinformatics analysis.基于生物信息学分析鉴定肺腺癌的关键基因和生物学通路。
Mol Cell Biochem. 2021 Feb;476(2):931-939. doi: 10.1007/s11010-020-03959-5. Epub 2020 Nov 1.
5
Fatal toxic effects related to EGFR tyrosine kinase inhibitors based on 53 cohorts with 9,569 participants.基于53个队列、9569名参与者的与表皮生长因子受体酪氨酸激酶抑制剂相关的致命毒性作用。
J Thorac Dis. 2020 Aug;12(8):4057-4069. doi: 10.21037/jtd-19-4000A.
6
Tyrosine kinase inhibitors interstitial pneumonitis: diagnosis and management.酪氨酸激酶抑制剂相关性间质性肺炎:诊断与管理
Transl Lung Cancer Res. 2019 Nov;8(Suppl 3):S318-S320. doi: 10.21037/tlcr.2019.05.02.
7
ASTRIS: a global real-world study of osimertinib in >3000 patients with T790M positive non-small-cell lung cancer.ASTRIS:一项全球真实世界研究,纳入了 >3000 例 T790M 阳性非小细胞肺癌患者,评估奥希替尼的疗效。
Future Oncol. 2019 Sep;15(26):3003-3014. doi: 10.2217/fon-2019-0324. Epub 2019 Jul 24.
8
Osimertinib-induced severe interstitial lung disease: A case report.奥希替尼致严重间质性肺疾病:一例报告。
Thorac Cancer. 2019 Jul;10(7):1657-1660. doi: 10.1111/1759-7714.13127. Epub 2019 Jun 26.
9
[EGFR-TKI ADR Management Chinese Expert Consensus].《表皮生长因子受体酪氨酸激酶抑制剂不良反应管理中国专家共识》
Zhongguo Fei Ai Za Zhi. 2019 Feb 20;22(2):57-81. doi: 10.3779/j.issn.1009-3419.2019.02.01.
10
Osimertinib in Untreated EGFR-Mutated Advanced Non-Small-Cell Lung Cancer.奥希替尼治疗未经治疗的 EGFR 突变型晚期非小细胞肺癌。
N Engl J Med. 2018 Jan 11;378(2):113-125. doi: 10.1056/NEJMoa1713137. Epub 2017 Nov 18.