Sumiya Ryusuke, Banno Takamitsu, Ueno Hiroyasu, Hirayama Shunki, Suzuki Kenji
Department of General Thoracic Surgery, Juntendo University Nerima Hospital, Tokyo 177-8521, Japan.
Department of General Thoracic Surgery, Juntendo University School of Medicine, Tokyo 113-0033, Japan.
Mol Clin Oncol. 2025 Apr 23;22(6):59. doi: 10.3892/mco.2025.2854. eCollection 2025 Jun.
Although nintedanib, an anti-fibrotic drug, relieves the chronological worsening of pulmonary function and prevents acute exacerbations of interstitial pneumonia, the perioperative safety and efficacy of nintedanib remains to be elucidated. The present study aimed to examine the safety and efficacy of nintedanib in patients with interstitial pneumonia. This study included 12 patients who underwent lung resection, including bilobectomy (n=2), lobectomy (n=7), segmentectomy (n=2) and wedge resection (n=1) between January 2020 and August 2023 at Juntendo University Nerima Hospital (Tokyo, Japan). Nintedanib was administered preoperatively to 10 male and two female patients with idiopathic pulmonary fibrosis and stage I to III lung cancer. The nintedanib dosing period ranged from 14 to 43 days. None of the patients canceled or postponed surgery because of side effects of nintedanib. Although prolonged air leak (n=3), surgical site infection (n=2), pyothorax (n=1), heart failure (n=1) and pleurisy (n=1) were observed postoperatively, the 30-day mortality rate was 0, with no acute exacerbation of interstitial pneumonia. These results encourage further investigation into the potential of nintedanib treatment in a larger patient cohort through prospective verification.
尽管抗纤维化药物尼达尼布可缓解肺功能随时间的恶化,并预防间质性肺炎的急性加重,但其围手术期的安全性和有效性仍有待阐明。本研究旨在探讨尼达尼布在间质性肺炎患者中的安全性和有效性。本研究纳入了2020年1月至2023年8月在日本东京顺天堂大学练马医院接受肺切除术的12例患者,包括双肺叶切除术(n = 2)、肺叶切除术(n = 7)、肺段切除术(n = 2)和楔形切除术(n = 1)。10例男性和2例女性特发性肺纤维化合并Ⅰ至Ⅲ期肺癌患者在术前接受了尼达尼布治疗。尼达尼布给药期为14至43天。没有患者因尼达尼布的副作用取消或推迟手术。尽管术后观察到有3例出现持续性漏气、2例出现手术部位感染、1例出现脓胸、1例出现心力衰竭和1例出现胸膜炎,但30天死亡率为0,且无间质性肺炎急性加重。这些结果鼓励通过前瞻性验证,在更大的患者队列中进一步研究尼达尼布治疗的潜力。