Suppr超能文献

奥希替尼诱发的间质性肺病在一名接受过纳武单抗预处理的非小细胞肺癌患者中的病例报告

Osimertinib-induced interstitial lung disease in a patient with non-small cell lung cancer pretreated with nivolumab: A case report.

作者信息

Takakuwa Osamu, Oguri Tetsuya, Uemura Takehiro, Sone Kazuki, Fukuda Satoshi, Okayama Minami, Kanemitsu Yoshihiro, Ohkubo Hirotsugu, Takemura Masaya, Ito Yutaka, Maeno Ken, Niimi Akio

机构信息

Department of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.

出版信息

Mol Clin Oncol. 2017 Sep;7(3):383-385. doi: 10.3892/mco.2017.1349. Epub 2017 Jul 25.

Abstract

Osimertinib (AZD9291) is a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor approved for EGFR-T790M-positive non-small cell lung cancer. A high incidence of interstitial lung disease (ILD) during combination treatment with osimertinib and anti-programmed cell death-ligand 1 (PD-L1) inhibitor has been reported. The current study presents a case of ILD development during osimertinib treatment following nivolumab (an anti-PD-1 antibody) treatment. The 59-year-old female was diagnosed with stage IV lung adenocarcinoma harboring a deletion in exon 19 of the EGFR gene. Following nivolumab as a sixth-line treatment, an EGFR-T790M-encoding mutation in EGFR exon 20 was identified by re-biopsy. Osimertinib was therefore initiated as a seventh-line treatment. A partial response was subsequently noted; however, 63 days after initiation of the treatment the patient presented with dyspnea with decreased oxygenation in the absence of fever and sputum. A computed tomography scan revealed the emergence of ground-glass opacities with bronchiectasis in both lungs, and a diagnosis of ILD due to osimertinib was made. Following steroid pulse therapy with discontinuation of osimertinib, the patient's chest findings and respiratory condition improved. Therefore, it is considered that anti-PD-1 therapies may be associated with a risk of ILD during subsequent osimertinib treatment.

摘要

奥希替尼(AZD9291)是一种第三代表皮生长因子受体(EGFR)酪氨酸激酶抑制剂,被批准用于治疗EGFR-T790M阳性的非小细胞肺癌。据报道,在奥希替尼与抗程序性细胞死亡配体1(PD-L1)抑制剂联合治疗期间,间质性肺疾病(ILD)的发生率较高。本研究报告了1例在接受纳武利尤单抗(一种抗PD-1抗体)治疗后使用奥希替尼治疗期间发生ILD的病例。该59岁女性被诊断为IV期肺腺癌,EGFR基因第19外显子存在缺失。在接受纳武利尤单抗作为第六线治疗后,通过再次活检在EGFR第20外显子中发现了编码EGFR-T790M的突变。因此,开始使用奥希替尼作为第七线治疗。随后观察到部分缓解;然而,在治疗开始63天后,患者出现呼吸困难,氧合下降,无发热和咳痰。计算机断层扫描显示双肺出现磨玻璃影伴支气管扩张,诊断为奥希替尼所致的ILD。在停用奥希替尼并给予类固醇冲击治疗后,患者的胸部检查结果和呼吸状况有所改善。因此,认为抗PD-1治疗可能与随后奥希替尼治疗期间发生ILD的风险相关。

相似文献

10
A "triple whammy" in adenocarcinoma lung.肺癌腺癌中的“三重打击”。
Lung India. 2019 Jul-Aug;36(4):340-344. doi: 10.4103/lungindia.lungindia_212_18.

引用本文的文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验