Ikeda Satoshi, Sekine Akimasa, Baba Tomohisa, Yamakawa Hideaki, Morita Masato, Kitamura Hideya, Ogura Takashi
Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, Tomioka-Higashi 6-16-1, Kanazawa-ku, Yokohama, 236-0051, Japan.
BMC Pulm Med. 2016 Mar 3;16:38. doi: 10.1186/s12890-016-0201-9.
Nintedanib is a multi-target receptor tyrosine kinase inhibitor. In two recent randomized phase 3 trials (INPULSIS™-1 and -2), it has been shown to slow the disease progression of idiopathic pulmonary fibrosis (IPF) by reducing the decline in the forced vital capacity (FVC). Although the INPULSIS™ trials indicate that nintedanib may serve to prevent acute exacerbations or delay the time to the first acute exacerbation, a certain number of IPF patients develop acute exacerbations while receiving nintedanib. However, there has been no report on the readministration of nintedanib in IPF patients who develop acute exacerbations during initial treatment with nintedanib.
A 64-year-old man with IPF had nintedanib added to his ongoing pirfenidone therapy. He developed dyspnea after 65 days and presented with hypoxemia after 68 days. At presentation, chest computed tomography showed newly developed diffuse ground glass opacities with the pre-existing subpleural reticular shadows. Because of the absence of infection or other potential causative factors, we diagnosed an acute exacerbation of IPF. Nintedanib was temporarily discontinued and the acute exacerbation was successfully managed with intensive treatment. We re-initiated nintedanib 30 days after cessation, which helped stabilize his FVC for 8 months. Nintedanib was safely continued for 28 months until he died of a bacterial infection.
To the best of our our knowledge, this is the first reported case of an acute exacerbation of IPF during nintedanib treatment, wherein nintedanib was safely and successfully restarted after treatment of the acute exacerbation. Our case indicates that nintedanib can be safely resumed and a desired effect on FVC can be obtained, even in IPF patients who develop acute exacerbations. However, we recommend close monitoring and appropriate measures until the long-term safety profile is clarified.
尼达尼布是一种多靶点受体酪氨酸激酶抑制剂。在最近的两项随机3期试验(INPULSIS™-1和-2)中,已证明它可通过减少用力肺活量(FVC)的下降来减缓特发性肺纤维化(IPF)的疾病进展。尽管INPULSIS™试验表明尼达尼布可能有助于预防急性加重或延迟首次急性加重的时间,但仍有一定数量的IPF患者在接受尼达尼布治疗时出现急性加重。然而,对于在初始治疗期间出现急性加重的IPF患者再次使用尼达尼布的情况,尚无相关报道。
一名64岁的IPF男性患者,在正在进行的吡非尼酮治疗基础上加用了尼达尼布。65天后出现呼吸困难,68天后出现低氧血症。就诊时,胸部计算机断层扫描显示新出现的弥漫性磨玻璃影以及原有的胸膜下网状阴影。由于没有感染或其他潜在病因,我们诊断为IPF急性加重。尼达尼布暂时停用,通过强化治疗成功控制了急性加重。停药30天后重新开始使用尼达尼布,这使他的FVC稳定了8个月。尼达尼布安全持续使用了28个月,直至他死于细菌感染。
据我们所知,这是首例报道的尼达尼布治疗期间IPF急性加重的病例,其中在急性加重治疗后安全且成功地重新开始使用了尼达尼布。我们的病例表明,即使是在出现急性加重的IPF患者中,尼达尼布也可以安全恢复使用并获得对FVC的预期效果。然而,在长期安全性明确之前,我们建议密切监测并采取适当措施。