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Deep Learning Algorithm Trained with COVID-19 Pneumonia Also Identifies Immune Checkpoint Inhibitor Therapy-Related Pneumonitis

Authors :
Bruno Beomonte Zobel
Daniele Santini
Marco Russano
Bruno Vincenzi
Yipeng Sun
Andrea Napolitano
Carlo Cosimo Quattrocchi
Gennaro Castiello
Carlo Augusto Mallio
Mario Iozzino
Silvia Angeletti
Francesco Maria Giordano
Giuseppe Tonini
Pasquale D'Alessio
Source :
Cancers, Vol 13, Iss 652, p 652 (2021), Cancers, Volume 13, Issue 4
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

Background: Coronavirus disease 2019 (COVID-19) pneumonia and immune checkpoint inhibitor (ICI) therapy-related pneumonitis share common features. The aim of this study was to determine on chest computed tomography (CT) images whether a deep convolutional neural network algorithm is able to solve the challenge of differential diagnosis between COVID-19 pneumonia and ICI therapy-related pneumonitis. Methods: We enrolled three groups: a pneumonia-free group (n = 30), a COVID-19 group (n = 34), and a group of patients with ICI therapy-related pneumonitis (n = 21). Computed tomography images were analyzed with an artificial intelligence (AI) algorithm based on a deep convolutional neural network structure. Statistical analysis included the Mann–Whitney U test (significance threshold at p &lt<br />0.05) and the receiver operating characteristic curve (ROC curve). Results: The algorithm showed low specificity in distinguishing COVID-19 from ICI therapy-related pneumonitis (sensitivity 97.1%, specificity 14.3%, area under the curve (AUC) = 0.62). ICI therapy-related pneumonitis was identified by the AI when compared to pneumonia-free controls (sensitivity = 85.7%, specificity 100%, AUC = 0.97). Conclusions: The deep learning algorithm is not able to distinguish between COVID-19 pneumonia and ICI therapy-related pneumonitis. Awareness must be increased among clinicians about imaging similarities between COVID-19 and ICI therapy-related pneumonitis. ICI therapy-related pneumonitis can be applied as a challenge population for cross-validation to test the robustness of AI models used to analyze interstitial pneumonias of variable etiology.

Details

Language :
English
ISSN :
20726694
Volume :
13
Issue :
652
Database :
OpenAIRE
Journal :
Cancers
Accession number :
edsair.doi.dedup.....9d1ca5b60b4705e802261e1acbc970f1