Prediction of neoadjuvant chemoradiotherapy response in rectal cancer with metric learning using pretreatment 18f-fluorodeoxyglucose positron emission tomography

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Abstract

Objectives: Neoadjuvant chemoradiotherapy (NCRT) followed by surgery is the mainstay of treatment for patients with locally advanced rectal cancer. Based on baseline 18F-fluorodeoxy-glucose ([18F]-FDG)-positron emission tomography (PET)/computed tomography (CT), a new artificial intelligence model using metric learning (ML) was introduced to predict responses to NCRT. Patients and Methods: This study used the data of 236 patients with newly diagnosed rectal cancer; the data of 202 and 34 patients were for training and validation, respectively. All patients received pretreatment [18F]FDG-PET/CT, NCRT, and surgery. The treatment response was scored by Dworak tumor regression grade (TRG); TRG3 and TRG4 indicated favorable responses. The model employed ML combined with the Uniform Manifold Approximation and Projection for dimensionality reduction. A receiver operating characteristic (ROC) curve analysis was performed to assess the model’s predictive performance. Results: In the training cohort, 115 patients (57%) achieved TRG3 or TRG4 responses. The area under the ROC curve was 0.96 for the prediction of a favorable response. The sensitivity, specificity, and accuracy were 98.3%, 96.5%, and 97.5%, respectively. The sensitivity, specificity, and accuracy for the validation cohort were 95.0%, 100%, and 98.8%, respectively. Conclusions: The new ML model presented herein was used to determined that baseline 18F[FDG]-PET/CT images could predict a favorable response to NCRT in patients with rectal cancer. External validation is required to verify the model’s predictive value.

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Wu, K. C., Chen, S. W., Hsieh, T. C., Yen, K. Y., Law, K. M., Kuo, Y. C., … Kao, C. H. (2021). Prediction of neoadjuvant chemoradiotherapy response in rectal cancer with metric learning using pretreatment 18f-fluorodeoxyglucose positron emission tomography. Cancers, 13(24). https://doi.org/10.3390/cancers13246350

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