Predicting High-risk Lung Adenocarcinoma in Solid and Part-solid Nodules on Low-dose CT: A Multicenter Study

  • 0Department of Radiology, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, Affiliated Cancer Hospital of University of Electronic Science and Technology of China, Chengdu, China (J.L., Y.L., Y.L., L.G., H.Q., P.Z.).

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Summary

This summary is machine-generated.

A new radiomic model using low-dose CT (LDCT) accurately identifies high-risk lung adenocarcinomas (LUADs) in solid and part-solid nodules. This non-invasive approach aids in early detection and decision-making for lung cancer screening.

Area Of Science

  • Radiology and Oncology
  • Medical Imaging Analysis
  • Artificial Intelligence in Medicine

Background

  • High-risk features in lung adenocarcinomas (LUADs) like visceral pleural invasion and lymph node metastasis are linked to poor prognosis.
  • Accurate identification of these high-risk LUADs is crucial for timely and effective patient management.

Purpose Of The Study

  • To develop and validate a radiomic model and a radiographic model using low-dose CT (LDCT) for predicting high-risk LUADs.
  • To compare the diagnostic performance of the radiomic and radiographic models in identifying high-risk LUADs within solid and part-solid nodules.

Main Methods

  • Retrospective analysis of 658 pathologically confirmed LUADs across four centers.
  • Construction of radiomic and radiographic models using multivariable logistic regression based on extracted features.
  • Validation of model performance using internal and external datasets, assessed by Area Under the Receiver Operating Characteristic Curve (AUC).

Main Results

  • The radiomic model incorporated three key features: GLCM_Correlation, GLSZM_SmallAreaEmphasis, and GLDM_LargeDependenceHighGrayLevelEmphasis.
  • The radiographic model included maximal diameter, consolidation/tumor ratio (CTR), spiculation, and pleural indentation.
  • The radiomic model demonstrated superior diagnostic performance with AUCs of 0.916 (internal) and 0.938 (external), significantly outperforming the radiographic model (0.868 and 0.880, respectively).

Conclusions

  • The developed LDCT-based radiomic model effectively identifies high-risk LUADs in solid and part-solid nodules.
  • This non-invasive radiomic model shows promising diagnostic performance.
  • The model may support personalized decision-making within lung cancer screening programs.