Kato Yoshiki, Ogawa Takunori, Sato Kimiya, Matsukida Akira, Kawana Akihiko, Nagaoka Ryosuke, Esaki Kotoba, Kimizuka Yoshifumi
Division of Infectious Diseases and Respiratory Medicine, Department of Internal Medicine National Defense Medical College Saitama Japan.
Department of Basic Pathology National Defense Medical College Saitama Japan.
Respirol Case Rep. 2025 Jun 23;13(6):e70241. doi: 10.1002/rcr2.70241. eCollection 2025 Jun.
The mesenchymal-epithelial transition exon 14 (ex14) skipping mutation is a driver of non-small cell lung cancer (NSCLC). MET tyrosine kinase inhibitors (TKIs), such as tepotinib, are effective against ex14 skipping-positive NSCLC but carry a risk of acute exacerbation of interstitial lung disease (AE-ILD) in patients with idiopathic pulmonary fibrosis (IPF). Here, we present a case of a 54-year-old man with IPF and ex14 skipping-positive lung adenocarcinoma. Following first-line platinum-based chemotherapy, disease control was not achieved for either lung cancer or IPF. Therefore, the patient underwent second-line treatment with tepotinib and the antifibrotic agent nintedanib. This combination effectively controlled both lung cancer and IPF, resulting in a partial response without AE-ILD. Our case suggests that nintedanib treatment may offer a safe and effective option for progressive IPF during MET-TKI therapy, presenting a novel therapeutic approach for patients with lung cancer complicated by IPF.
间充质-上皮转化外显子14(ex14)跳跃突变是非小细胞肺癌(NSCLC)的驱动因素。甲磺酸特泊替尼等MET酪氨酸激酶抑制剂(TKIs)对ex14跳跃阳性NSCLC有效,但对特发性肺纤维化(IPF)患者有发生间质性肺病急性加重(AE-ILD)的风险。在此,我们报告一例54岁男性,患有IPF且ex14跳跃阳性肺腺癌。一线铂类化疗后,肺癌和IPF均未实现疾病控制。因此,该患者接受了甲磺酸特泊替尼和抗纤维化药物尼达尼布的二线治疗。这种联合治疗有效地控制了肺癌和IPF,产生了部分缓解且未发生AE-ILD。我们的病例表明,尼达尼布治疗可能为MET-TKI治疗期间进展性IPF提供一种安全有效的选择,为合并IPF的肺癌患者提供了一种新的治疗方法。