Ning Mao

Prof. Dr. Ning Mao


Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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2 May 2025 in Science Advances
Verified
Journal Article
Open access
NMNing Mao
Ning Mao
YDYi Dai
Yi Dai
HZHeng Zhou
Heng Zhou
FLFan Lin
Fan Lin
TZTiantian Zheng
Tiantian Zheng
JLJie Lu
Jie Lu
Accurately predicting pathological complete response (pCR) before neoadjuvant chemotherapy (NAC) is crucial for patients with breast cancer. In this study, we developed a multimodal integrated fully automated pipeline system (MIFAPS) in forecasting pCR to NAC, using a multicenter and prospective dataset of 1004 patients with locally advanced breast cancer, incorporating pretreatment magnetic resonance imaging, whole slide image, and clinical risk factors. The results demonstrated that MIFAPS offered a favorable predictive performance in both the pooled external test set [area under the curve (AUC) = 0.882] and the prospective test set (AUC = 0.909). In addition, MIFAPS significantly outperformed single-modality models ( P < 0.05). Furthermore, the high deep learning scores were associated with immune-related pathways and the promotion of antitumor cells in the microenvironment during biological basis exploration. Overall, our study demonstrates a promising approach for improving the prediction of pCR to NAC in patients with breast cancer through the integration of multimodal data.

13 May 2023 in European Radiology
Verified
Journal Article
Closed access
PDF file
CWCai Wang
Cai Wang
PYPengyi Yu
Pengyi Yu
HZHaicheng Zhang
Haicheng Zhang
XHXiao Han
Xiao Han
ZSZheying Song
Zheying Song
XSXicheng Song
Xicheng Song

30 August 2024 in Biological Psychiatry
Verified
Journal Article
Closed access
TCTongpeng Chu
Tongpeng Chu
XSXiaopeng Si
Xiaopeng Si
HXHaizhu Xie
Haizhu Xie
HMHeng Ma
Heng Ma
YSYinghong Shi
Yinghong Shi
NMNing Mao
Ning Mao

4 April 2023 in European Radiology
Verified
Journal Article
Closed access
PDF file
SZShijie Zhang
Shijie Zhang
HSHuafei Shao
Huafei Shao
WLWenjuan Li
Wenjuan Li
HZHaicheng Zhang
Haicheng Zhang
FLFan Lin
Fan Lin
NMNing Mao
Ning Mao

30 October 2020 in Frontiers in Oncology
Verified
Journal Article
Open access
PDF file
FLFan Lin
Fan Lin
ZWZhongyi Wang
Zhongyi Wang
KZKun Zhang
Kun Zhang
PYPing Yang
Ping Yang
HMHeng Ma
Heng Ma
NMNing Mao
Ning Mao
Objectives: To develop a radiomics nomogram that incorporates contrast-enhanced spectral mammography (CESM)-based radiomics features and clinico-radiological variables for identifying benign and malignant breast lesions of sub-1 cm. Methods: This retrospective study included 139 patients with the diameter of sub-1 cm on cranial caudal (CC) position of recombined images. Radiomics features were extracted from low-energy and recombined images on CC position. The variance threshold, analysis of variance (ANOVA) and least absolute shrinkage and selection operator (LASSO) algorithms were used to select optimal predictive features. Radiomics signature (Rad-score) was calculated by a linear combination of selected features. The independent predictive factors were identified by ANOVA and multivariate logistic regression. A radiomics nomogram was developed to predict the malignant probability of lesions. The performance and clinical utility of the nomogram was evaluated by receiver operating characteristic (ROC) curve, calibration curve, and decision curve analysis (DCA). Results: Nineteen radiomics features were selected to calculate Rad-score. Breast imaging reporting and data system (BI-RADS) category and age were identified as predictive factors. The radiomics nomogram combined with Rad-score, BI-RADS category, and age showed better performance (area under curves [AUC]: 0.940, 95% confidence interval [CI]: 0.804–0.992) than Rad-score (AUC: 0.868, 95% CI: 0.711–0.958) and clinico-radiological model (AUC: 0.864, 95% CI: 0.706–0.956) in the validation cohort. The calibration curve and DCA showed that the radiomics nomogram had good consistency and clinical utility. Conclusions: The radiomics nomogram incorporated with CESM-based radiomics features, BI-RADS category and age could identify benign and malignant breast lesions of sub-1 cm.

1 January 2020 in BioMed Research International
Verified
Journal Article
Open access
PDF file
YDYi Dai
Yi Dai
PYPing Yin
Ping Yin
NMNing Mao
Ning Mao
CSChao Sun
Chao Sun
JWJiangfen Wu
Jiangfen Wu
NHNan Hong
Nan Hong
Objective. To determine if osteosarcoma (OS) and Ewing sarcoma (EWS) of the pelvis based on MRI can be differentiated using radiomic analysis. Materials and Methods. In this study, 3.0 T magnetic resonance (MR) data of 66 patients (40 males and 26 females, mean age 27.6 ± 13.9 years) with pathologically confirmed OS or EWS of the pelvis (35 with OS and 31 with EWS) taken from April 2013 to December 2017 were retrospectively reviewed. T2‐weighted fat‐saturated (T2‐FS) and contrast‐enhanced T1‐weighted (CET1) images were manually segmented, and imaging features were extracted. Independent‐sample t‐test, Spearman’s test, and the least absolute shrinkage and selection operator (LASSO) method were used to select the most useful features from the original data set. The performance of radiomic analysis was investigated by the area under the receiver operating characteristic (ROC) curve (AUC) analysis. Results. 385 initial features were extracted from T2‐FS and CET1 MR data. Nine features from T2‐FS and 7 features from CET1 were selected by using the LASSO method. The radiomic analysis to differentiate OS and EWS of the pelvis based on T2‐FS and CET1 images using the aforementioned selected features achieved AUC values of 0.881 (95% confidence interval (CI): 0.799–0.963) and 0.765 (95% CI: 0.652–0.878), respectively. Conclusion. Radiomic analysis showed potential in differentiating OS from EWS of the pelvis, in which T2‐FS demonstrated better diagnostic value. To differentiate OS from EWS of the pelvis using our multiparametric MRI‐based radiomic analysis could preoperatively improve diagnostic accuracy and greatly contribute to therapy planning.