4.1 Article

18F-FDG-PET/MRI texture analysis in rectal cancer after neoadjuvant chemoradiotherapy

Journal

NUCLEAR MEDICINE COMMUNICATIONS
Volume 43, Issue 7, Pages 815-822

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MNM.0000000000001570

Keywords

neoadjuvant chemoradiotherapy; PET; MRI; radiology; rectal cancer; surgery

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This study assessed the ability of 18F-FDG PET/MRI to predict the response to nCRT in patients with locally advanced rectal cancer. The results showed that PET/MRI texture analysis is a valuable tool for identifying patients with a complete pathological response to nCRT.
Objective Reliable markers to predict the response to neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal cancer (LARC) are lacking. We aimed to assess the ability of 18F-FDG PET/MRI to predict response to nCRT among patients undergoing curative-intent surgery. Methods Patients with histological-confirmed LARC who underwent curative-intent surgery following nCRT and restaging with 18F-FDG PET/MRI were included. Statistical correlation between radiomic features extracted in PET, apparent diffusion coefficient (ADC) and T2w images and patients' histopathologic response to chemoradiotherapy using a multivariable logistic regression model ROC-analysis. Results Overall, 50 patients were included in the study. A pathological complete response was achieved in 28.0% of patients. Considering second-order textural features, nine parameters showed a statistically significant difference between the two groups in ADC images, six parameters in PET images and four parameters in T2w images. Combining all the features selected for the three techniques in the same multivariate ROC curve analysis, we obtained an area under ROC curve of 0.863 (95% CI, 0.760-0.966), showing a sensitivity, specificity and accuracy at the Youden's index of 100% (14/14), 64% (23/36) and 74% (37/50), respectively. Conclusion PET/MRI texture analysis seems to represent a valuable tool in the identification of rectal cancer patients with a complete pathological response to nCRT.

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