Matsuki Rei, Okuda Kenichi, Mitani Akihisa, Yamauchi Yasuhiro, Tanaka Goh, Kume Haruki, Homma Yukio, Hinata Munetoshi, Hayashi Akimasa, Shibahara Junji, Fukayama Masashi, Nagase Takahide
Department of Respiratory Medicine, The University of Tokyo Hospital, Japan.
Department of Urology, The University of Tokyo Hospital, Japan.
Respir Med Case Rep. 2017 Aug 11;22:158-163. doi: 10.1016/j.rmcr.2017.08.008. eCollection 2017.
Temsirolimus is an inhibitor of mammalian target of rapamycin and interstitial lung disease (ILD) is known to be one of the adverse events associated with temsirolimus, which usually improves rapidly after discontinuation of the drug and rarely worsens thereafter. Herein, we report a case of delayed exacerbation of ILD after discontinuation of temsirolimus for metastatic renal cell carcinoma in an 86-year-old male with chronic ILD. The patient developed gradually worsening dyspnea five weeks after an initiation of temsirolimus and was admitted to our facility. On his admission, although a pulmonary function test revealed a decreased diffusion capacity, there was no obvious progression of ILD on HRCT scan. His dyspnea once improved after discontinuation of temsirolimus, but it recurred and acute exacerbation of ILD was diagnosed 40 days after his last administration of temsirolimus. He received high-dose steroid therapy, however, he deteriorated and died. Histopathological examination of the lungs at autopsy revealed overlapping diffuse alveolar damage with chronic interstitial changes. In the present case, since there were no specific factors that could have caused acute exacerbation of ILD except for temsirolimus, it was considered to contribute to the exacerbation of underlying ILD. In conclusion, physicians should be aware of the possibility of temsirolimus-induced ILD not only while the medication is administered, but also even after it is discontinued. It is important to carefully interview the patient and to recognize the value of physiological tests, such as respiratory function tests and blood gas analysis, as well as imaging findings on HRCT.
替西罗莫司是一种哺乳动物雷帕霉素靶蛋白抑制剂,间质性肺病(ILD)是已知与替西罗莫司相关的不良事件之一,通常在停药后迅速改善,此后很少恶化。在此,我们报告一例86岁患有慢性ILD的男性患者,因转移性肾细胞癌停用替西罗莫司后发生ILD延迟加重的病例。该患者在开始使用替西罗莫司五周后逐渐出现呼吸困难加重,并入住我院。入院时,尽管肺功能测试显示弥散功能下降,但HRCT扫描显示ILD无明显进展。停用替西罗莫司后他的呼吸困难一度改善,但又复发,在最后一次使用替西罗莫司40天后被诊断为ILD急性加重。他接受了大剂量类固醇治疗,然而,病情仍恶化并死亡。尸检时肺部的组织病理学检查显示弥漫性肺泡损伤与慢性间质改变并存。在本病例中,除替西罗莫司外,没有其他可能导致ILD急性加重的特定因素,因此认为它促成了潜在ILD的加重。总之,医生不仅在用药期间,而且在停药后都应意识到替西罗莫司诱发ILD的可能性。仔细询问患者并认识到呼吸功能测试和血气分析等生理检查以及HRCT影像学表现的价值很重要。