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奥希替尼致严重双侧气胸:病例报告。

Osimertinib-induced severe bilateral pneumothorax: A case report.

机构信息

Department of Respiration, The Third Hospital of Hebei Medical University, Shijiazhuang, China.

出版信息

Medicine (Baltimore). 2024 Jan 19;103(3):e36994. doi: 10.1097/MD.0000000000036994.

Abstract

RATIONALE

Osimertinib is the third-generation, pyrimidine-based, irreversible epidermal growth factor receptor-tyrosine kinase inhibitor that received approval from the FDA in November 2015 and has become the standard approach in patients with advanced, epidermal growth factor receptor (EGFR) mutated non-small cell lung cancer (NSCLC), especially with brain metastases. Osimertinib is beneficial in terms of progression-free and overall survival in patients with EGFR-mutated NSCLC. However, the rarity of bilateral pneumothorax among adverse events necessitates further research on its potential fatality rate.

PATIENT CONCERNS

A 72-year-old man diagnosed with stage IV (T2NxM1) NSCLC with the 21L858R mutation of the EGFR gene received osimertinib treatment. Unfortunately, 10 weeks after osimertinib treatment, the patient developed severe interstitial lung disease and pneumothorax. Thus, osimertinib treatment was discontinued, and prednisolone (160 mg/day) and supportive treatment were administered.

DIAGNOSES

Osimertinib-induced severe interstitial lung disease and pneumothorax.

INTERVENTIONS

Osimertinib treatment was discontinued, and prednisolone (160 mg/day) and supportive treatment were administered.

OUTCOMES

The bilateral pneumothorax was difficult to correct and the patient eventually died.

LESSONS

Osimertinib-induced pneumothorax occurred approximately 10 weeks after receiving the drug and had severe cough and chest tightness as initial symptoms. In addition, the incidence of drug-induced pneumothorax increases in patients treated with osimertinib when combined with underlying respiratory diseases.

摘要

背景

奥希替尼是第三代、嘧啶类、不可逆的表皮生长因子受体酪氨酸激酶抑制剂,于 2015 年 11 月获得 FDA 批准,已成为晚期表皮生长因子受体(EGFR)突变型非小细胞肺癌(NSCLC)患者的标准治疗方法,尤其是有脑转移的患者。奥希替尼在 EGFR 突变型 NSCLC 患者的无进展生存期和总生存期方面均有益。然而,其不良事件中双侧气胸的罕见性需要进一步研究其潜在死亡率。

病例介绍

一名 72 岁男性,诊断为 IV 期(T2NxM1)NSCLC,EGFR 基因 21L858R 突变,接受奥希替尼治疗。不幸的是,奥希替尼治疗 10 周后,患者出现严重间质性肺病和气胸。因此,停止奥希替尼治疗,并给予泼尼松龙(160mg/天)和支持治疗。

诊断

奥希替尼引起的严重间质性肺病和气胸。

干预措施

停止奥希替尼治疗,并给予泼尼松龙(160mg/天)和支持治疗。

结果

双侧气胸难以纠正,患者最终死亡。

教训

奥希替尼诱导的气胸在用药后约 10 周发生,最初症状为严重咳嗽和胸闷。此外,在接受奥希替尼治疗的患者中,合并基础呼吸系统疾病时,药物诱导性气胸的发生率增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2c/10798711/622a95555370/medi-103-e36994-g001.jpg

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