Reproducible and Interpretable Spiculation Quantification for Lung Cancer Screening
This work addresses lung cancer screening by providing a reproducible and interpretable method for spiculation quantification, which is incremental as it builds on existing radiomics frameworks with new features.
The study tackled the problem of quantifying spiculations on lung nodules to predict cancer malignancy by proposing an interpretable, parameter-free technique using area distortion from conformal spherical parameterization, achieving AUCs of 0.80 and 0.76 on validation datasets, outperforming previous models with AUC=0.68.
Spiculations are important predictors of lung cancer malignancy, which are spikes on the surface of the pulmonary nodules. In this study, we proposed an interpretable and parameter-free technique to quantify the spiculation using area distortion metric obtained by the conformal (angle-preserving) spherical parameterization. We exploit the insight that for an angle-preserved spherical mapping of a given nodule, the corresponding negative area distortion precisely characterizes the spiculations on that nodule. We introduced novel spiculation scores based on the area distortion metric and spiculation measures. We also semi-automatically segment lung nodule (for reproducibility) as well as vessel and wall attachment to differentiate the real spiculations from lobulation and attachment. A simple pathological malignancy prediction model is also introduced. We used the publicly-available LIDC-IDRI dataset pathologists (strong-label) and radiologists (weak-label) ratings to train and test radiomics models containing this feature, and then externally validate the models. We achieved AUC$=$0.80 and 0.76, respectively, with the models trained on the 811 weakly-labeled LIDC datasets and tested on the 72 strongly-labeled LIDC and 73 LUNGx datasets; the previous best model for LUNGx had AUC$=$0.68. The number-of-spiculations feature was found to be highly correlated (Spearman's rank correlation coefficient $ρ= 0.44$) with the radiologists' spiculation score. We developed a reproducible and interpretable, parameter-free technique for quantifying spiculations on nodules. The spiculation quantification measures was then applied to the radiomics framework for pathological malignancy prediction with reproducible semi-automatic segmentation of nodule. Using our interpretable features (size, attachment, spiculation, lobulation), we were able to achieve higher performance than previous models.