Kirkil Gamze, Mogulkoc Nesrin, Jovanovic Dragana
Department of Chest Disease, University of Firat, Elazig, Türkiye.
Department of Chest Disease, University of Ege, İzmir, Türkiye.
Sarcoidosis Vasc Diffuse Lung Dis. 2025 Mar 18;42(1):15604. doi: 10.36141/svdld.v42i1.15604.
Idiopathic pulmonary fibrosis (IPF) is a fatal lung disease. Lung cancer (LC) is among the most crucial comorbidity factors in patients with IPF. IPF patients that are diagnosed with LC have a reduced mean survival time. Therapeutic strategies for LC in patients with IPF need to be adapted according to the individual treatment risk. Life-threatening acute exacerbation (AE) of IPF may occur in association with cancer treatment, thereby severely restricting the therapeutic options for IPF-associated LC. Because LC and anticancer treatments can worsen the prognosis of IPF, the prevention of LC is as critical as managing patients with IPF.
特发性肺纤维化(IPF)是一种致命的肺部疾病。肺癌(LC)是IPF患者最重要的合并症因素之一。被诊断为LC的IPF患者平均生存时间缩短。IPF患者中LC的治疗策略需要根据个体治疗风险进行调整。IPF的危及生命的急性加重(AE)可能与癌症治疗相关,从而严重限制了IPF相关LC的治疗选择。由于LC和抗癌治疗会使IPF的预后恶化,预防LC与管理IPF患者同样重要。