Prediction of micropapillary and solid pattern in lung adenocarcinoma using radiomic values extracted from near-pure histopathological subtypes.


Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 12 06 2020
accepted: 26 11 2020
revised: 01 10 2020
pubmed: 4 1 2021
medline: 24 6 2021
entrez: 3 1 2021
Statut: ppublish

Résumé

Near-pure lung adenocarcinoma (ADC) subtypes demonstrate strong stratification of radiomic values, providing basic information for pathological subtyping. We sought to predict the presence of high-grade (micropapillary and solid) components in lung ADCs using quantitative image analysis with near-pure radiomic values. Overall, 103 patients with lung ADCs of various histological subtypes were enrolled for 10-repetition, 3-fold cross-validation (cohort 1); 55 were enrolled for testing (cohort 2). Histogram and textural features on computed tomography (CT) images were assessed based on the "near-pure" pathological subtype data. Patch-wise high-grade likelihood prediction was performed for each voxel within the tumour region. The presence of high-grade components was then determined based on a volume percentage threshold of the high-grade likelihood area. To compare with quantitative approaches, consolidation/tumour (C/T) ratio was evaluated on CT images; we applied radiological invasiveness (C/T ratio > 0.5) for the prediction. In cohort 1, patch-wise prediction, combined model (C/T ratio and patch-wise prediction), whole-lesion-based prediction (using only the "near-pure"-based prediction model), and radiological invasiveness achieved a sensitivity and specificity of 88.00 ± 2.33% and 75.75 ± 2.82%, 90.00 ± 0.00%, and 77.12 ± 2.67%, 66.67% and 90.41%, and 90.00% and 45.21%, respectively. The sensitivity and specificity, respectively, for cohort 2 were 100.0% and 95.35% using patch-wise prediction, 100.0% and 95.35% using combined model, 75.00% and 95.35% using whole-lesion-based prediction, and 100.0% and 69.77% using radiological invasiveness. Using near-pure radiomic features and patch-wise image analysis demonstrated high levels of sensitivity and moderate levels of specificity for high-grade ADC subtype-detecting. • The radiomic values extracted from lung adenocarcinoma with "near-pure" histological subtypes provide useful information for high-grade (micropapillary and solid) components detection. • Using near-pure radiomic features and patch-wise image analysis, high-grade components of lung adenocarcinoma can be predicted with high sensitivity and moderate specificity. • Using near-pure radiomic features and patch-wise image analysis has potential role in facilitating the prediction of the presence of high-grade components in lung adenocarcinoma prior to surgical resection.

Identifiants

pubmed: 33389033
doi: 10.1007/s00330-020-07570-6
pii: 10.1007/s00330-020-07570-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5127-5138

Subventions

Organisme : National Taiwan University, Hsin-Chu Branch (TW)
ID : 108-HCH061
Organisme : Ministry of Science and Technology, Taiwan
ID : 107-2221-E-002-074-MY3
Organisme : Ministry of Science and Technology, Taiwan
ID : 107-2221-E-002-080-MY3

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Auteurs

Li-Wei Chen (LW)

Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd., Taipei, 10617, Taiwan.

Shun-Mao Yang (SM)

Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd., Taipei, 10617, Taiwan.
Department of Surgery, National Taiwan University Hospital Biomedical Park Hospital, No. 2, Sec.1, Shengyi Rd., Zhubei City, Hsinchu County, 302, Taiwan.

Hao-Jen Wang (HJ)

Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd., Taipei, 10617, Taiwan.

Yi-Chang Chen (YC)

Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd., Taipei, 10617, Taiwan.
Department of Medical Imaging, National Taiwan University Hospital and National Taiwan University College of Medicine, No. 1, Sec. 1, Jen - Ai Rd., Taipei, 100, Taiwan.

Mong-Wei Lin (MW)

Department of Surgery, National Taiwan University Hospital and National Taiwan University College of Medicine, No. 1, Sec. 1, Jen - Ai Rd., Taipei, 100, Taiwan.

Min-Shu Hsieh (MS)

Department of Pathology, National Taiwan University Hospital and National Taiwan University College of Medicine, No. 1, Sec. 1, Jen - Ai Rd., Taipei, 100, Taiwan.

Hsiang-Lin Song (HL)

Department of Pathology, National Taiwan University Hospital, Hsin-Chu Branch, No. 25, Lane 442, Sec.1, Jingguo Rd., Hsinchu, 300, Taiwan.

Huan-Jang Ko (HJ)

Department of Surgery, National Taiwan University Hospital, Hsin-Chu Branch, No. 25, Lane 442, Sec.1, Jingguo Rd., Hsinchu, 300, Taiwan.

Chung-Ming Chen (CM)

Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd., Taipei, 10617, Taiwan. chung@ntu.edu.tw.

Yeun-Chung Chang (YC)

Department of Medical Imaging, National Taiwan University Hospital, 7 Chung-Shan South Road, Taipei, Taiwan. ycc5566@ntu.edu.tw.

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