Abstract
OBJECTIVE: Accurately identifying patients achieving pathological complete response (pCR) after neoadjuvant chemoradiotherapy (nCRT) for locally advanced rectal cancer (LARC) not only ensures treatment efficacy but also helps avoid surgical risks. We developed a comprehensive multi-omics model to predict pCR before surgery. METHODS: Clinical data, CT, MRI-T1WI and MRI-T2WI, and radiotherapy dose were collected from 183 LARC patients who underwent preoperative nCRT. Backward stepwise selection, logistic regression, and five-fold cross-validation were employed for the development and validation of a non-imaging model, three radiomics-based models and a dosiomics-based model. These were integrated into a final model, and its performance was tested on multi-center sets. RESULTS: C_model, based on clinical characteristics, achieved an AUC of 0.85 in the validation set. Radiomics models (CT_model, T1_model, T2_model) exhibited AUCs of 0.66, 0.67, and 0.64, respectively. Dosiomics-based model, D_model, achieved an AUC of 0.75 in validation. The mean AUCs for F_model in the training sets, validation sets, internal and external test sets were 0.90, 0.88, 0.77, and 0.74, respectively. CONCLUSION: To assess the efficacy of nCRT in LARC patients, it is crucial to consider clinical characteristics, followed by dosiomics. While T1_model, T2_model and CT_model demonstrate relatively comparable performance, each contributes unique value to the final prediction model.