Impact of accurate diagnosis of interstitial lung diseases on postoperative outcomes in lung cancer

Objective The prognostic impact of interstitial lung disease (ILD) subclassification based on both high-resolution computed tomography (HRCT) scan findings and histopathological findings is unknown. Methods We retrospectively analyzed 104 patients who were diagnosed with clinical ILD according to HR...

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Veröffentlicht in:General thoracic and cardiovascular surgery 2023-02, Vol.71 (2), p.129-137
Hauptverfasser: Azuma, Yoko, Sakamoto, Susumu, Homma, Sakae, Sano, Atsushi, Sakai, Takashi, Koezuka, Satoshi, Otsuka, Hajime, Tochigi, Naobumi, Kishi, Kazuma, Iyoda, Akira
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container_end_page 137
container_issue 2
container_start_page 129
container_title General thoracic and cardiovascular surgery
container_volume 71
creator Azuma, Yoko
Sakamoto, Susumu
Homma, Sakae
Sano, Atsushi
Sakai, Takashi
Koezuka, Satoshi
Otsuka, Hajime
Tochigi, Naobumi
Kishi, Kazuma
Iyoda, Akira
description Objective The prognostic impact of interstitial lung disease (ILD) subclassification based on both high-resolution computed tomography (HRCT) scan findings and histopathological findings is unknown. Methods We retrospectively analyzed 104 patients who were diagnosed with clinical ILD according to HRCT scan findings and who underwent lung cancer surgery. Via an expert multidisciplinary discussion, we re-classified HRCT scan findings and validated the histopathological patterns of ILDs in lung specimens. Results There were several mismatches between HRCT scan findings and histological patterns. Moreover, 87 (83.7%) and 6 (5.8%) patients were diagnosed with definitive ILD and pathological non-ILD, respectively. Finally, 82 patients with idiopathic interstitial pneumonias (IIPs) were divided into the idiopathic pulmonary fibrosis (IPF) ( n  = 61) group and the other group ( n  = 21). The 5-year overall survival rate of the IPF group was significantly lower than that of the other group (22.8% vs 67.9%; p  = 0.011). Sub-classification of IIPs was found to be an independent prognostic factor for overall survival in patients with lung cancer. Conclusion An accurate diagnosis of IIPs/IPF according to both HRCT scan findings and histological patterns is important for providing an appropriate treatment among patients with lung cancer who presented with clinical ILD.
doi_str_mv 10.1007/s11748-022-01868-6
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Methods We retrospectively analyzed 104 patients who were diagnosed with clinical ILD according to HRCT scan findings and who underwent lung cancer surgery. Via an expert multidisciplinary discussion, we re-classified HRCT scan findings and validated the histopathological patterns of ILDs in lung specimens. Results There were several mismatches between HRCT scan findings and histological patterns. Moreover, 87 (83.7%) and 6 (5.8%) patients were diagnosed with definitive ILD and pathological non-ILD, respectively. Finally, 82 patients with idiopathic interstitial pneumonias (IIPs) were divided into the idiopathic pulmonary fibrosis (IPF) ( n  = 61) group and the other group ( n  = 21). The 5-year overall survival rate of the IPF group was significantly lower than that of the other group (22.8% vs 67.9%; p  = 0.011). Sub-classification of IIPs was found to be an independent prognostic factor for overall survival in patients with lung cancer. Conclusion An accurate diagnosis of IIPs/IPF according to both HRCT scan findings and histological patterns is important for providing an appropriate treatment among patients with lung cancer who presented with clinical ILD.</description><identifier>ISSN: 1863-6705</identifier><identifier>EISSN: 1863-6713</identifier><identifier>DOI: 10.1007/s11748-022-01868-6</identifier><identifier>PMID: 35999412</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Cancer therapies ; Cardiac Surgery ; Cardiology ; Classification ; Cysts ; Fibroblasts ; Humans ; Idiopathic Interstitial Pneumonias ; Idiopathic Pulmonary Fibrosis - diagnosis ; Idiopathic Pulmonary Fibrosis - diagnostic imaging ; Lung - pathology ; Lung cancer ; Lung diseases ; Lung Diseases, Interstitial - diagnosis ; Lung Neoplasms - complications ; Lung Neoplasms - diagnosis ; Lung Neoplasms - surgery ; Medical prognosis ; Medicine ; Medicine &amp; Public Health ; Normal distribution ; Original ; Original Article ; Patients ; Pneumonia ; Retrospective Studies ; Surgery ; Surgical Oncology ; Thoracic Surgery ; Tomography</subject><ispartof>General thoracic and cardiovascular surgery, 2023-02, Vol.71 (2), p.129-137</ispartof><rights>The Author(s) 2022</rights><rights>2022. 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Methods We retrospectively analyzed 104 patients who were diagnosed with clinical ILD according to HRCT scan findings and who underwent lung cancer surgery. Via an expert multidisciplinary discussion, we re-classified HRCT scan findings and validated the histopathological patterns of ILDs in lung specimens. Results There were several mismatches between HRCT scan findings and histological patterns. Moreover, 87 (83.7%) and 6 (5.8%) patients were diagnosed with definitive ILD and pathological non-ILD, respectively. Finally, 82 patients with idiopathic interstitial pneumonias (IIPs) were divided into the idiopathic pulmonary fibrosis (IPF) ( n  = 61) group and the other group ( n  = 21). The 5-year overall survival rate of the IPF group was significantly lower than that of the other group (22.8% vs 67.9%; p  = 0.011). Sub-classification of IIPs was found to be an independent prognostic factor for overall survival in patients with lung cancer. 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Methods We retrospectively analyzed 104 patients who were diagnosed with clinical ILD according to HRCT scan findings and who underwent lung cancer surgery. Via an expert multidisciplinary discussion, we re-classified HRCT scan findings and validated the histopathological patterns of ILDs in lung specimens. Results There were several mismatches between HRCT scan findings and histological patterns. Moreover, 87 (83.7%) and 6 (5.8%) patients were diagnosed with definitive ILD and pathological non-ILD, respectively. Finally, 82 patients with idiopathic interstitial pneumonias (IIPs) were divided into the idiopathic pulmonary fibrosis (IPF) ( n  = 61) group and the other group ( n  = 21). The 5-year overall survival rate of the IPF group was significantly lower than that of the other group (22.8% vs 67.9%; p  = 0.011). Sub-classification of IIPs was found to be an independent prognostic factor for overall survival in patients with lung cancer. Conclusion An accurate diagnosis of IIPs/IPF according to both HRCT scan findings and histological patterns is important for providing an appropriate treatment among patients with lung cancer who presented with clinical ILD.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>35999412</pmid><doi>10.1007/s11748-022-01868-6</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0908-4840</orcidid><oa>free_for_read</oa></addata></record>
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subjects Cancer therapies
Cardiac Surgery
Cardiology
Classification
Cysts
Fibroblasts
Humans
Idiopathic Interstitial Pneumonias
Idiopathic Pulmonary Fibrosis - diagnosis
Idiopathic Pulmonary Fibrosis - diagnostic imaging
Lung - pathology
Lung cancer
Lung diseases
Lung Diseases, Interstitial - diagnosis
Lung Neoplasms - complications
Lung Neoplasms - diagnosis
Lung Neoplasms - surgery
Medical prognosis
Medicine
Medicine & Public Health
Normal distribution
Original
Original Article
Patients
Pneumonia
Retrospective Studies
Surgery
Surgical Oncology
Thoracic Surgery
Tomography
title Impact of accurate diagnosis of interstitial lung diseases on postoperative outcomes in lung cancer
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