Towards the use of multiple ROIs for radiomics-based survival modelling: finding a strategy of aggregating lesions

TL;DR

This study investigates strategies for integrating multiple lesions' radiomic features into survival models, demonstrating that including all lesions improves predictive performance in lung cancer prognosis.

Contribution

It proposes methods to aggregate radiomic data from multiple lesions and validates their effectiveness in enhancing survival prediction models.

Findings

Including all lesions improves model c-index.

Aggregating features from multiple lesions enhances predictive accuracy.

Lesions beyond primary tumors carry valuable prognostic information.

Abstract

Background. Radiomic features, derived from a region of interest (ROI) in medical images, are valuable as prognostic factors. Selecting an appropriate ROI is critical, and many recent studies have focused on leveraging multiple ROIs by segmenting analogous regions across patients - such as the primary tumour and peritumoral area or subregions of the tumour. These can be straightforwardly incorporated into models as additional features. However, a more complex scenario arises for example in a regionally disseminated disease, when multiple distinct lesions are present. Aim. This study aims to evaluate the feasibility of integrating radiomic data from multiple lesions into survival models. We explore strategies for incorporating these ROIs and hypothesise that including all available lesions can improve model performance. Methods. While each lesion produces a feature vector, the desired result is a unified prediction. We propose methods to aggregate either the feature vectors to form a representative ROI or the modeling results to compute a consolidated risk score. As a proof of concept, we apply these strategies to predict distant metastasis risk in a cohort of 115 non-small cell lung cancer patients, 60% of whom exhibit regionally advanced disease. Two feature sets (radiomics extracted from PET and PET interpolated to CT resolution) are tested across various survival models using a Monte Carlo Cross-Validation framework. Results. Across both feature sets, incorporating all available lesions - rather than limiting analysis to the primary tumour - consistently improved the c-index, irrespective of the survival model used. Conclusion. Lesions beyond the primary tumour carry information that should be utilised in radiomics-based models to enhance predictive ability.