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Multi-sequence MRI radiomics of colorectal liver metastases: Which features are reproducible across readers?

Denise J van der Reijd ,
Kalina Chupetlovska ,
Eleanor van Dijk ,
Bram Westerink ,
Melanie A Monraats ,
Joost J M Van Griethuysen ,
Doenja M J Lambregts ,
Renaud Tissier ,
Regina G H Beets-Tan ,
Sean Benson ,
Monique Maas

Abstract

CONCLUSIONS

The majority of MRI radiomics features from CE-T1W, T2W, DWI and ADC in colorectal liver metastases were robust for segmentation variability between readers. The CE-T1W yielded slightly better reproducibility results compared to DWI and T2W. The ADC features seem more susceptible to reader differences compared to the other three sequences.

RESULTS

90% of CE-T1W features were reproducible with a median ICC of 0.98 (range 0.76-1.00). 81% of DWI features were robust with median ICC = 0.97 (range 0.38-1.00). The T2W features had a median ICC of 0.96 (range 0.55-0.99) and were reproducible in 80%. ADC showed the lowest number of reproducible features with 58% and median ICC = 0.91 (range 0.38-0.99) When considering the lower bound of the ICC 95% confidence intervals, 58%, 66%, 54% and 29% reached 0.9 for the CE-T1W, DWI, T2W and ADC features, respectively. The feature class with the best reproducibility differed per sequence.

METHOD

30 CRLM (in 23 patients) were manually delineated by three readers on MRI before the start of chemotherapy on the contrast enhanced T1-weighted images (CE-T1W) in the portal venous phase, T2-weighted images (T2W) and b800 diffusion weighted images (DWI). DWI delineations were copied to the ADC-maps. 107 radiomics features were extracted per sequence. The intraclass correlation coefficient (ICC) was calculated per feature. Features were considered reproducible if ICC > 0.9.

PURPOSE

To assess the inter-reader reproducibility of radiomics features on multiple MRI sequences after segmentations of colorectal liver metastases (CRLM).

More about this publication

European journal of radiology

Volume 172
Pages 111346
Publication date 01-03-2024

Full text links

Publisher website (DOI) 10.1016/j.ejrad.2024.111346
Europe PubMed Central 38309217
Pubmed 38309217

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