LLLonggao Liu

Longgao Liu

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Longgao Liu has a total of 9 co-authors. Here are the top co-authors by number of shared publications:

  • Chufeng Zeng

    Sun Yat-sen University Cancer Center, 651 Dongfeng Road East, Guangzhou 510060, China

    1 shared publication
  • Jianhua Fu

    Department of Thoracic Oncology Sun Yat‐sen University Cancer Center Guangzhou China

    1 shared publication
  • Lizhi Liu

    Department of Radiology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer Sun Yat‐Sen University Cancer Center Guangzhou Guangdong China

    1 shared publication
  • Peng Lin

    Sun Yat-sen University Cancer Center, 651 Dongfeng Road East, Guangzhou 510060, China

    1 shared publication
  • Shumin Zhou

    Department of Radiology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou 510060, China

    1 shared publication
  • Tiehua Rong

    Sun Yat-sen University Cancer Center, 651 Dongfeng Road East, Guangzhou 510060, China

    1 shared publication

Latest Publications

  • Open Access

    Multimodal CT and MRI Radiomics Integrated with Clinical Models Predict Pathological Complete Response in ESCC Following Neoadjuvant Immunochemotherapy

    by Longgao Liu, Chufeng Zeng, Lizhi Liu, Shumin Zhou, Weihua Wu, Peng Lin, Jianhua Fu, Tiehua Rong, Xu Zhang, Xiaodong Su

    Background: This research focused on evaluating the utility of multimodal radiomics integrated with machine learning to predict pathological complete response (pCR) in a prospective cohort of esophageal squamous cell carcinoma (ESCC) patients undergoing neoadjuvant immunochemotherapy (nICT). Methods: We retrospectively analyzed prospectively collected trial data from 66 ESCC patients. Radiomic features were extracted from computed tomography (CT) and magnetic resonance imaging (MRI) images. Four machine learning algorithms—Random Forest (RF), logistic regression, Support Vector Machine, and Extreme Gradient Boosting (XGBoost)—were applied with leave-one-out cross-validation to predict pCR after nICT. The predictive performance of the models was evaluated using receiver operating characteristic curve analysis. Results: In total, 851 features were identified. Among the four machine learning algorithms, the XGBoost machine learning method demonstrated the best model performance across CT, MRI, and clinical feature-based models. Furthermore, the integrated model demonstrated superior performance compared to individual models based solely on CT, MRI, or clinical features across all machine learning algorithms. Among these, the XGboost-based integrated model achieved the highest performance on the test set, with an AUC of 0.961, a TPR of 84.2%, a TNR of 95.7%, a PPV 88.9% of and a NPV of 93.8%. Decision curve analysis validated the model’s robust clinical utility, with calibration curves demonstrating strong concordance between predicted and observed therapeutic responses. Conclusions: The study demonstrates the potential for predicting pCR in patients with ESCC treated with standardized neoadjuvant chemotherapy and PD-1 inhibitors using machine learning methods that integrate multimodal CT and MRI images with clinical features.