Prediction of lung malignancy progression and survival with machine learning based on pre-treatment FDG-PET/CT.


Journal

EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 25 07 2021
revised: 16 05 2022
accepted: 09 06 2022
pubmed: 11 7 2022
medline: 17 8 2022
entrez: 10 7 2022
Statut: ppublish

Résumé

Pre-treatment FDG-PET/CT scans were analyzed with machine learning to predict progression of lung malignancies and overall survival (OS). A retrospective review across three institutions identified patients with a pre-procedure FDG-PET/CT and an associated malignancy diagnosis. Lesions were manually and automatically segmented, and convolutional neural networks (CNNs) were trained using FDG-PET/CT inputs to predict malignancy progression. Performance was evaluated using area under the receiver operating characteristic curve (AUC), accuracy, sensitivity, and specificity. Image features were extracted from CNNs and by radiomics feature extraction, and random survival forests (RSF) were constructed to predict OS. Concordance index (C-index) and integrated brier score (IBS) were used to evaluate OS prediction. 1168 nodules (n=965 patients) were identified. 792 nodules had progression and 376 were progression-free. The most common malignancies were adenocarcinoma (n=740) and squamous cell carcinoma (n=179). For progression risk, the PET+CT ensemble model with manual segmentation (accuracy=0.790, AUC=0.876) performed similarly to the CT only (accuracy=0.723, AUC=0.888) and better compared to the PET only (accuracy=0.664, AUC=0.669) models. For OS prediction with deep learning features, the PET+CT+clinical RSF ensemble model (C-index=0.737) performed similarly to the CT only (C-index=0.730) and better than the PET only (C-index=0.595), and clinical only (C-index=0.595) models. RSF models constructed with radiomics features had comparable performance to those with CNN features. CNNs trained using pre-treatment FDG-PET/CT and extracted performed well in predicting lung malignancy progression and OS. OS prediction performance with CNN features was comparable to a radiomics approach. The prognostic models could inform treatment options and improve patient care. NIH NHLBI training grant (5T35HL094308-12, John Sollee).

Sections du résumé

BACKGROUND BACKGROUND
Pre-treatment FDG-PET/CT scans were analyzed with machine learning to predict progression of lung malignancies and overall survival (OS).
METHODS METHODS
A retrospective review across three institutions identified patients with a pre-procedure FDG-PET/CT and an associated malignancy diagnosis. Lesions were manually and automatically segmented, and convolutional neural networks (CNNs) were trained using FDG-PET/CT inputs to predict malignancy progression. Performance was evaluated using area under the receiver operating characteristic curve (AUC), accuracy, sensitivity, and specificity. Image features were extracted from CNNs and by radiomics feature extraction, and random survival forests (RSF) were constructed to predict OS. Concordance index (C-index) and integrated brier score (IBS) were used to evaluate OS prediction.
FINDINGS RESULTS
1168 nodules (n=965 patients) were identified. 792 nodules had progression and 376 were progression-free. The most common malignancies were adenocarcinoma (n=740) and squamous cell carcinoma (n=179). For progression risk, the PET+CT ensemble model with manual segmentation (accuracy=0.790, AUC=0.876) performed similarly to the CT only (accuracy=0.723, AUC=0.888) and better compared to the PET only (accuracy=0.664, AUC=0.669) models. For OS prediction with deep learning features, the PET+CT+clinical RSF ensemble model (C-index=0.737) performed similarly to the CT only (C-index=0.730) and better than the PET only (C-index=0.595), and clinical only (C-index=0.595) models. RSF models constructed with radiomics features had comparable performance to those with CNN features.
INTERPRETATION CONCLUSIONS
CNNs trained using pre-treatment FDG-PET/CT and extracted performed well in predicting lung malignancy progression and OS. OS prediction performance with CNN features was comparable to a radiomics approach. The prognostic models could inform treatment options and improve patient care.
FUNDING BACKGROUND
NIH NHLBI training grant (5T35HL094308-12, John Sollee).

Identifiants

pubmed: 35810561
pii: S2352-3964(22)00308-5
doi: 10.1016/j.ebiom.2022.104127
pmc: PMC9278031
pii:
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104127

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests Dr. Feng reports personal fees from Carina Medical LLC, outside the submitted work. The remaining authors declare that they have no conflicts of interest and nothing to disclose.

Auteurs

Brian Huang (B)

Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.

John Sollee (J)

Warren Alpert Medical School of Brown University, Providence, RI 02903, USA; Department of Diagnostic Radiology, Rhode Island Hospital, 593 Eddy St. Providence, Providence, RI 02903, USA.

Yong-Heng Luo (YH)

Department of Radiology, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, China.

Ashwin Reddy (A)

Warren Alpert Medical School of Brown University, Providence, RI 02903, USA; Department of Diagnostic Radiology, Rhode Island Hospital, 593 Eddy St. Providence, Providence, RI 02903, USA.

Zhusi Zhong (Z)

School of Electronic Engineering, Xidian University, Xi'an 710071, China.

Jing Wu (J)

Department of Radiology, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, China.

Joseph Mammarappallil (J)

Department of Diagnostic Radiology, Duke University School of Medicine, Durham, NC 27708, USA.

Terrance Healey (T)

Warren Alpert Medical School of Brown University, Providence, RI 02903, USA; Department of Diagnostic Radiology, Rhode Island Hospital, 593 Eddy St. Providence, Providence, RI 02903, USA.

Gang Cheng (G)

Department of Diagnostic Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.

Christopher Azzoli (C)

Department of Thoracic Oncology, Rhode Island Hospital, Providence, RI 02903, USA.

Dana Korogodsky (D)

Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.

Paul Zhang (P)

Department of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.

Xue Feng (X)

Carina Medical Inc., Lexington, KY 40507, USA.

Jie Li (J)

School of Electronic Engineering, Xidian University, Xi'an 710071, China.

Li Yang (L)

Department of Neurology, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, China. Electronic address: Yangli762@csu.edu.cn.

Zhicheng Jiao (Z)

Warren Alpert Medical School of Brown University, Providence, RI 02903, USA; Department of Diagnostic Radiology, Rhode Island Hospital, 593 Eddy St. Providence, Providence, RI 02903, USA.

Harrison Xiao Bai (HX)

Department of Radiology and Radiological Sciences, Johns Hopkins University, 601 N. Carolina St., Baltimore, MD 21287, USA.

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Classifications MeSH