Atezolizumab and nintedanib in patients with non-small cell lung cancer and interstitial lung disease

被引:1
|
作者
Yamaguchi, Teppei [1 ]
Shimizu, Junichi [1 ]
Shigematsu, Fumie [1 ]
Watanabe, Naohiro [1 ]
Hasegawa, Takaaki [2 ]
Horio, Yoshitsugu [1 ]
Inaba, Yoshitaka [2 ]
Fujiwara, Yutaka [1 ]
机构
[1] Aichi Canc Ctr Hosp, Dept Thorac Oncol, 1-1 Kanokoden,Chikusa Ku, Nagoya, Aichi 4648681, Japan
[2] Aichi Canc Ctr Hosp, Dept Diagnost & Intervent Radiol, Nagoya, Japan
关键词
Nintedanib; atezolizumab; interstitial lung disease (ILD); immunotherapy; non-small cell lung cancer (NSCLC); PULMONARY-FIBROSIS; DOCETAXEL; NIVOLUMAB; PNEUMONITIS; PHASE-3;
D O I
10.21037/jtd-24-45
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
In patients with non -small cell lung cancer (NSCLC), pre-existing interstitial lung disease (ILD) is a risk factor for the development of pneumonitis induced by immune checkpoint inhibitors (ICIs). Antifibrotic agents, including nintedanib, reduce the potential for acute exacerbation of idiopathic pulmonary fibrosis (IPF). However, whether nintedanib can reduce the potential for ICI -induced pneumonitis is unknown. From among 140 patients with NSCLC treated with atezolizumab monotherapy at our institution, we retrospectively investigated 4 patients with pre-existing ILD treated concurrently with nintedanib. On computed tomography (CT), a usual interstitial pneumonia (UIP) pattern was present in one patient, probable UIP pattern in one patient, and indeterminate for UIP pattern in two patients. Of those four patients with pre-existing ILD, two achieved a partial response to ICI treatment, with response durations of 8.1 and 7.6 months. The other two patients experienced progressive disease. Notable adverse events included the development of non -symptomatic grade 1 pneumonitis in the patient with a probable UIP pattern and grade 3 lower gastrointestinal hemorrhage in another patient. None of the patients experienced a worsening of respiratory symptoms. In patients with NSCLC and pre-existing ILD, nintedanib might reduce the potential for ICI -induced pneumonitis and enhance the antitumor effect.
引用
收藏
页码:3371 / 3380
页数:10
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