Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Front Oncol ; 14: 1333020, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38347846

RESUMO

Objective: To develop and validate a multiparametric MRI-based radiomics model for prediction of microsatellite instability (MSI) status in patients with endometrial cancer (EC). Methods: A total of 225 patients from Center I including 158 in the training cohort and 67 in the internal testing cohort, and 132 patients from Center II were included as an external validation cohort. All the patients were pathologically confirmed EC who underwent pelvic MRI before treatment. The MSI status was confirmed by immunohistochemistry (IHC) staining. A total of 4245 features were extracted from T2-weighted imaging (T2WI), contrast enhanced T1-weighted imaging (CE-T1WI) and apparent diffusion coefficient (ADC) maps for each patient. Four feature selection steps were used, and then five machine learning models, including Logistic Regression (LR), k-Nearest Neighbors (KNN), Naive Bayes (NB), Support Vector Machine (SVM), and Random Forest (RF), were built for MSI status prediction in the training cohort. Receiver operating characteristics (ROC) curve and decision curve analysis (DCA) were used to evaluate the performance of these models. Results: The SVM model showed the best performance with an AUC of 0.905 (95%CI, 0.848-0.961) in the training cohort, and was subsequently validated in the internal testing cohort and external validation cohort, with the corresponding AUCs of 0.875 (95%CI, 0.762-0.988) and 0.862 (95%CI, 0.781-0.942), respectively. The DCA curve demonstrated favorable clinical utility. Conclusion: We developed and validated a multiparametric MRI-based radiomics model with gratifying performance in predicting MSI status, and could potentially be used to facilitate the decision-making on clinical treatment options in patients with EC.

2.
Eur J Radiol ; 144: 109963, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34562744

RESUMO

PURPOSE: This study aimed to evaluate the potential role of diffusion kurtosis imaging (DKI)-derived parameters for assessing resistance to CRT in patients with Locally advanced rectal cancer (LARC) by using histogram analysis derived from whole-tumor volumes. METHOD: 136 consecutive patients with histologically confirmed rectal adenocarcinoma who underwent MRI examination before and after chemoradiotherapy were enrolled in our retrospective study. The parameters D, K, and conventional apparent diffusion coefficient (ADC) were measured using whole-tumor volume histogram analysis. The AJCC tumor regression grading (TRG) system was the standard reference (resistance: TRG 3; non-resistance: TRG 0-2). Receiver operating characteristic (ROC) curves were used for evaluating the diagnostic performance. RESULTS: Aside from the skew and kurtosis values, we found all the histogram metrics of D and ADC values significantly increased after CRT (all p < 0.001). In contrast, the histogram metrics of K values significantly decreased after CRT. The majority of percentiles metrics of D, K, and ADC values were correlated with tumor resistance before and after CRT (P < 0.05), except for the skew and kurtosis values. Regarding the comparison of the diagnostic performance of all the histogram metrics, the percentage Dmean change (ΔDmean) showed the highest AUC value of 0.939, and the corresponding sensitivity, specificity, PPV, and NPV were 84.1% and 94.6%, 88.1% and 92.6%, respectively. CONCLUSIONS: These preliminary results demonstrated that DKI-derived histogram metrics, especially the pre-treatment metrics and ΔDmean, were useful to assess tumoral resistance to CRT and individual clinical management for patients with LARC.


Assuntos
Adenocarcinoma , Neoplasias Retais , Adenocarcinoma/diagnóstico por imagem , Adenocarcinoma/terapia , Benchmarking , Quimiorradioterapia , Imagem de Difusão por Ressonância Magnética , Humanos , Terapia Neoadjuvante , Neoplasias Retais/tratamento farmacológico , Neoplasias Retais/terapia , Estudos Retrospectivos , Sensibilidade e Especificidade
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...