4.7 Article

Preoperative CT-based radiomics combined with intraoperative frozen section is predictive of invasive adenocarcinoma in pulmonary nodules: a multicenter study

Journal

EUROPEAN RADIOLOGY
Volume 30, Issue 5, Pages 2680-2691

Publisher

SPRINGER
DOI: 10.1007/s00330-019-06597-8

Keywords

Carcinoma; non-small-cell lung; Machine learning; Frozen sections; Adenocarcinoma of lung; Tomography; spiral computed

Funding

  1. China Scholarships Council [201808210318]
  2. ERC advanced grant (ERC-ADG-2015) [694812 -Hypoximmuno]
  3. ERC-2018PoC [81320 -CL-IO]
  4. Dutch technology Foundation STW [P14-19]
  5. Technology Programme of the Ministry of Economic Affairs
  6. SME Phase 2 (RAIL) [673780]
  7. EUROSTARS (DART, DECIDE, COMPACT)
  8. European Program H2020-201517 (ImmunoSABR) [733008]
  9. European Program H2020-201517 (PREDICT -ITN) [766276]
  10. TRANSCAN Joint Transnational Call 2016 (JTC2016 CLEARLY) [UM 2017-8295]
  11. Interreg V-A Euregio Meuse-Rhine (Euradiomics)
  12. Kankeronderzoekfonds Limburg (KOFL) from the Health Foundation Limburg
  13. Dutch Cancer Society

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Objectives Develop a CT-based radiomics model and combine it with frozen section (FS) and clinical data to distinguish invasive adenocarcinomas (IA) from preinvasive lesions/minimally invasive adenocarcinomas (PM). Methods This multicenter study cohort of 623 lung adenocarcinomas was split into training (n = 331), testing (n = 143), and external validation dataset (n = 149). Random forest models were built using selected radiomics features, results from FS, lesion volume, clinical and semantic features, and combinations thereof. The area under the receiver operator characteristic curves (AUC) was used to evaluate model performances. The diagnosis accuracy, calibration, and decision curves of models were tested. Results The radiomics-based model shows good predictive performance and diagnostic accuracy for distinguishing IA from PM, with AUCs of 0.89, 0.89, and 0.88, in the training, testing, and validation datasets, respectively, and with corresponding accuracies of 0.82, 0.79, and 0.85. Adding lesion volume and FS significantly increases the performance of the model with AUCs of 0.96, 0.97, and 0.96, and with accuracies of 0.91, 0.94, and 0.93 in the three datasets. There is no significant difference in AUC between the FS model enriched with radiomics and volume against an FS model enriched with volume alone, while the former has higher accuracy. The model combining all available information shows minor non-significant improvements in AUC and accuracy compared with an FS model enriched with radiomics and volume. Conclusions Radiomics signatures are potential biomarkers for the risk of IA, especially in combination with FS, and could help guide surgical strategy for pulmonary nodules patients.

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