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使用抗PD1抗体治疗后奥希替尼诱发的间质性肺疾病。

Osimertinib-induced interstitial lung disease after treatment with anti-PD1 antibody.

作者信息

Mamesaya Nobuaki, Kenmotsu Hirotsugu, Katsumata Mineo, Nakajima Takashi, Endo Masahiro, Takahashi Toshiaki

机构信息

Division of Thoracic Oncology, Shizuoka Cancer Center Hospital, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka, 411-8777, Japan.

Department of Pulmonary Medicine, Seirei Hamamatsu General Hospital, Shizuoka, Japan.

出版信息

Invest New Drugs. 2017 Feb;35(1):105-107. doi: 10.1007/s10637-016-0389-9. Epub 2016 Sep 6.

DOI:10.1007/s10637-016-0389-9
PMID:27599705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5306260/
Abstract

We report a case of a 38-year-old woman who was diagnosed with stage IV lung adenocarcinoma, harboring an epidermal growth factor receptor (EGFR) L858R mutation on exon 21 and a T790 M mutation on exon 20. The patient was treated with osimertinib, a third-generation EGFR tyrosine kinase inhibitor (EGFR-TKI) following treatment with nivolumab, an anti-Programmed Cell Death 1 (anti-PD1) antibody. After initiating osimertinib treatment, the patient began to complain of low-grade fever and shortness of breath without hypoxemia, and her chest radiograph and a CT scan revealed a remarkable antitumor response, although faint infiltrations were observed in the bilateral lung field. Bronchoalveolar lavage fluid mainly contained lymphocytes (CD4+/CD8+ ratio of 0.3), and a transbronchial lung biopsy specimen showed lymphocytic alveolitis with partial organization in several alveolar spaces. Therefore we diagnosed the patient with osimertinib-induced interstitial lung disease (ILD) after treatment with anti-PD1 antibody. We considered anti-PD1 therapies may be the risk factor of EGFR-TKI-induced ILD.

摘要

我们报告了一例38岁女性患者,她被诊断为IV期肺腺癌,其21外显子存在表皮生长因子受体(EGFR)L858R突变,20外显子存在T790M突变。该患者在接受抗程序性细胞死亡蛋白1(anti-PD1)抗体纳武单抗治疗后,接受了第三代EGFR酪氨酸激酶抑制剂(EGFR-TKI)奥希替尼治疗。开始奥希替尼治疗后,患者开始抱怨低热和气短,但无低氧血症,其胸部X线片和CT扫描显示出显著的抗肿瘤反应,尽管在双侧肺野观察到轻微浸润。支气管肺泡灌洗液主要含有淋巴细胞(CD4+/CD8+比值为0.3),经支气管肺活检标本显示在几个肺泡腔中有淋巴细胞性肺泡炎伴部分机化。因此,我们诊断该患者在接受anti-PD1抗体治疗后发生了奥希替尼诱导的间质性肺疾病(ILD)。我们认为anti-PD1治疗可能是EGFR-TKI诱导的ILD的危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a6e/5306260/222536032bb1/10637_2016_389_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a6e/5306260/db2cf84d2e8b/10637_2016_389_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a6e/5306260/222536032bb1/10637_2016_389_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a6e/5306260/db2cf84d2e8b/10637_2016_389_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a6e/5306260/222536032bb1/10637_2016_389_Fig2_HTML.jpg

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本文引用的文献

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A real-world pharmacovigilance study of FDA Adverse Event Reporting System (FAERS) events for osimertinib.真实世界的奥希替尼不良事件报告系统(FAERS)药物警戒研究
Sci Rep. 2022 Nov 15;12(1):19555. doi: 10.1038/s41598-022-23834-1.
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Intern Med. 2021 Feb 15;60(4):591-594. doi: 10.2169/internalmedicine.5435-20. Epub 2020 Sep 30.