阿法替尼诱导的闭塞性支气管炎

IF 0.2 Q4 ONCOLOGY
Tadayuki Nakashima, Yoshimasa Shiraishi, Ayaka Shiota, Yasuto Yoneshima, Eiji Iwama, Kentaro Tanaka, Isamu Okamoto
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引用次数: 0

摘要

我们报告一例闭塞性细支气管炎(BO)由于阿法替尼治疗。一名42岁的女性被诊断为IVB期肺腺癌(cT1bN3M1c), EGFR L861Q突变阳性,并接受了阿法替尼治疗。在开始阿法替尼治疗7个月后,她出现咳嗽,尽管治疗支气管哮喘,但咳嗽逐渐加重。肺功能检查显示严重的阻塞性,吸入支气管扩张剂后没有改善。胸部计算机断层扫描显示马赛克衰减模式,肺通气灌注显像显示匹配的缺陷。她没有继发性BO的潜在原因,因此她被诊断为阿法替尼诱发的BO。停止阿法替尼或随后用奥西替尼治疗后,呼吸功能没有进一步恶化。本病例提示阿法替尼是BO的潜在诱因。因此,临床肿瘤学家应牢记,在接受阿法替尼治疗的患者中可能发生这种潜在的致命不良事件;他们应该警惕呼吸道症状,并考虑定期进行肺功能检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Afatinib-induced bronchiolitis obliterans

We report a case of bronchiolitis obliterans (BO) due to afatinib treatment. A 42-year-old woman was diagnosed with stage IVB lung adenocarcinoma (cT1bN3M1c) positive for the L861Q mutation of EGFR and was treated with afatinib. Seven months after the onset of afatinib therapy, she presented with a cough that gradually worsened despite treatment for bronchial asthma. Pulmonary function tests showed severe obstructive patterns that were not improved with inhaled bronchodilators. Chest computed tomography revealed a mosaic attenuation pattern, and pulmonary ventilation-perfusion scintigraphy showed a matched defect. She had no underlying causes of secondary BO, and she was therefore diagnosed with afatinib-induced BO. Respiratory function did not deteriorate further after discontinuation of afatinib or after subsequent treatment with osimertinib. This case indicates that afatinib is a potential trigger for BO. Clinical oncologists should therefore bear in mind the possible development of this potentially fatal adverse event in patients undergoing afatinib treatment; they should be alert to respiratory symptoms and consider periodic pulmonary function tests.

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CiteScore
0.40
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