Mingping Ma

Dr. Mingping Ma

Provincial Clinical College, Fujian Medical University, Fuzhou, Fujian, China

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 April 2023 in Quantitative Imaging in Medicine and Surgery
Verified
Journal Article
Open access
PDF file
MHMuzhen He
Muzhen He
JSJiawei Su
Jiawei Su
HRHuiping Ruan
Huiping Ruan
YSYang Song
Yang Song
MMMingping Ma
Mingping Ma
FXFangqin Xue
Fangqin Xue
Original Article Nomogram based on quantitative dynamic contrast-enhanced magnetic resonance imaging, apparent diffusion coefficient, and clinicopathological features for early prediction of pathologic complete response in breast cancer patients receiving neoadjuvant chemotherapy Muzhen He, Jiawei Su, Huiping Ruan, Yang Song, Mingping Ma, Fangqin Xue

11 April 2025 in Medical Physics
Verified
Journal Article
Open access
HZHui Zhang
Hui Zhang
YZYunyan Zheng
Yunyan Zheng
MZMingzhe Zhang
Mingzhe Zhang
AWAiling Wang
Ailing Wang
YSYang Song
Yang Song
MHMuzhen He
Muzhen He
Background: Radiomics research based on whole tumors is limited by the unclear biological significance of radiomics features, which therefore lack clinical interpretability. Purpose: We aimed to determine whether features extracted from subregions defined by habitat imaging, reflecting tumor heterogeneity, could identify breast cancer patients who will benefit from neoadjuvant chemotherapy (NAC), to optimize treatment. Methods: 143 women with stage II–III breast cancer were divided into a training set (100 patients, 36 with pathologic complete response [pCR]) and a test set (43 patients, 16 with pCR). Patients underwent 3‐T magnetic resonance imaging (MRI) before NAC. With the pathological results as the gold standard, we used the training set to build models for predicting pCR based on whole‐tumor radiomics (Model WH ), intravoxel incoherent motion (IVIM)‐based habitat imaging (Model Habitats ), conventional MRI features (Model CF ), and immunohistochemical findings (Model IHC ). We also built the combined models Model Habitats+CF and Model Habitats+CF+IHC . In the test set, we compared the performance of the combined models with that of the invasive Model IHC by using the area under the receiver operating characteristic curve (AUC) and decision curve analysis (DCA). Receiver operating characteristic (ROC) curve analysis was performed to evaluate the predictive value of the model. The DeLong test was used to compare diagnostic efficiency across different parameters. Results: In the prediction of pCR, Model WH , Model Habitats , Model CF , Model IHC , Model Habitats+CF , Model CF+IHC and Model Habitats+CF+IHC achieved AUCs of 0.895, 0.757, 0.705, 0.807, 0.800, 0.856, and 0.891 respectively, in the training set and 0.549, 0.708, 0.700, 0.788, 0.745, 0.909, and 0.891 respectively, in the test set. The DeLong test revealed no significant difference between Model IHC versus Model Habitats+CF ( p = 0.695) and Model Habitats+CF+IHC versus Model CF+IHC ( p = 0.382) but showed a significant difference between Model IHC and Model Habitats+CF+IHC ( p = 0.043). Conclusion: The habitat model we established from first‐order features combined with conventional MRI features and IHC findings accurately predicted pCR before NAC. This model can facilitate decision‐making during individualized treatment for breast cancer.

21 June 2021 in Frontiers in Oncology
Verified
Journal Article
Open access
PDF file
MHMuzhen He
Muzhen He
HRHuiping Ruan
Huiping Ruan
MMMingping Ma
Mingping Ma
ZZZhongshuai Zhang
Zhongshuai Zhang
To explore the value of apparent diffusion coefficient (ADC), intravoxel incoherent motion (IVIM), and diffusional kurtosis imaging (DKI) based on diffusion weighted magnetic resonance imaging (DW-MRI) in differentiating benign and malignant breast lesions. A total of 215 patients with breast lesions were prospectively collected for breast MR examination. Single exponential, IVIM, and DKI models were calculated using a series of b values. Parameters including ADC, perfusion fraction (f), tissue diffusion coefficient (D), perfusion-related incoherent microcirculation (D*), average kurtosis (MK), and average diffusivity (MD) were compared between benign and malignant lesions. ROC curves were used to analyze the optimal diagnostic threshold of each parameter, and to evaluate the diagnostic efficacy of single and combined parameters. ADC, D, MK, and MD values were significantly different between benign and malignant breast lesions (P<0.001). Among the single parameters, ADC had the highest diagnostic efficiency (sensitivity 91.45%, specificity 82.54%, accuracy 88.84%, AUC 0.915) and the best diagnostic threshold (0.983 μm2/ms). The combination of ADC and MK offered high diagnostic performance (sensitivity 90.79%, specificity 85.71%, accuracy 89.30%, AUC 0.923), but no statistically significant difference in diagnostic performance as compared with single-parameter ADC (P=0.268). The ADC, D, MK, and MD parameters have high diagnostic value in differentiating benign and malignant breast lesions, and of these individual parameters the ADC has the best diagnostic performance. Therefore, our study revealed that the use of ADC alone should be useful for differentiating between benign and malignant breast lesions, whereas the combination of MK and ADC might improve the diagnostic performance to some extent.

11 February 2025 in Frontiers in Oncology
Verified
Journal Article
Open access
PDF file
YZYunyan Zheng
Yunyan Zheng
HZHui Zhang
Hui Zhang
HCHuijian Chen
Huijian Chen
YSYang Song
Yang Song
PLPing Lu
Ping Lu
MHMuzhen He
Muzhen He
Background: To develop a predictive model using baseline imaging of morphology and radiomics derived from intravoxel incoherent motion diffusion-weighted imaging (IVIM-DWI) to determine the pathologic complete response (pCR) to neoadjuvant chemotherapy (NACT) in breast cancer patients.Methods: A total of 265 patients who underwent 3.0 T MRI scans before NACT were examined. Among them, 113 female patients with stage II–III breast cancer were included. The training data set consisted of 79 patients (31/48=pCR/Non-PCR, npCR), while the remaining 34 cases formed the validation cohort (13/21=pCR/npCR). Radiomics and conventional magnetic resonance imaging features analysis were performed. To build a nomogram model that integrates the radiomics signature and conventional imaging, a logistic regression method was employed. The performance evaluation of the nomogram involved the area under the receiver operating characteristic curve (AUC), a decision curve analysis, and the calibration slope.Results: In an assessment for predicting pCR, the radiomics model displayed an AUC of 0.778 and 0.703 for the training and testing cohorts, respectively. Conversely, the morphology model exhibited an AUC of 0.721 and 0.795 for the training and testing cohorts, respectively. The nomogram displayed superior predictive discrimination with an AUC of 0.862 for the training cohort and 0.861 for the testing cohort. Decision curve analyses indicated that the nomogram provided the highest clinical net benefit.Conclusion: Performing a nomogram consisting of integrated morphology and radiomics assessment using IVIM-DWI before NACT enables effective prediction of pCR in breast cancer. This predictive model therefore can facilitate medical professionals in making individualized treatment decisions.