Abstract 931P
Background
Currently, there is a paucity of validated deep learning methodologies for predicting short-term efficacy in locally advanced nasopharyngeal carcinoma (NPC), both domestically and internationally. Furthermore, advanced techniques such as 2.5D feature extraction and Transformer model establishment remain underexplored in this context.
Methods
MRI images from locally advanced NPC patients diagnosed at two centers between July 2020 and June 2023 were retrospectively collected. Three state-of-the-art (SOTA) models (SegResNet, Unet, and UnetR models) were employed for automatic segmentation of all regions of interest (ROIs), thus generating an automatic segmentation model. Leveraging 2.5D deep learning techniques, tumor image features were extracted and integrated into a transfer learning framework. Subsequently, a Transformer-based model was designed, integrating all individual patient features. Three models were established: a clinical model, a Transformer model, and a fusion model. The predictive performance of these models was evaluated using receiver operating characteristic (ROC) curves, calibration curves, and decision curve analysis (DCA).
Results
Among the three models, the Transformer model demonstrated superior predictive performance in both the testing (AUC = 0.957) and validation cohorts (AUC = 0.893) compared to the clinical model. Moreover, the fusion model generally matched or surpassed the performance of the Transformer model, particularly in the testing cohort with an AUC of 0.874, indicating that the integration of clinical data with advanced machine learning models can enhance predictive capability.
Conclusions
The fusion model, which combines machine learning with clinical factors, exhibits promising efficacy in predicting short-term outcomes in locally advanced NPC patients following synchronous chemoradiotherapy.
Clinical trial identification
Editorial acknowledgement
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
907P - Biomarker analysis of the phase III KEYNOTE-040 study of pembrolizumab (pembro) versus methotrexate, docetaxel, or cetuximab (SOC) for recurrent/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC)
Presenter: Denis Soulieres
Session: Poster session 03
909P - Immunoscore-IC predicts nivolumab efficacy as adjuvant treatment after salvage surgery in head and neck cancer squamous cell carcinoma: The ADJORL1 trial
Presenter: Alix Marhic
Session: Poster session 03
911P - Association of genomic landscape and plasma protein dynamic changes with clinical outcome in patients with R/M HNSCC treated with pembrolizumab with nab-paclitaxel and platinum
Presenter: Xinrui Chen
Session: Poster session 03
912P - Selection of personalized salvage treatments in advanced refractory head and neck squamous cell carcinomas via multi-omics tumor profiling
Presenter: Ramin Ajami
Session: Poster session 03
913P - Characterisation of genomic biomarkers of response to cetuximab versus cisplatin in concomitance with radiotherapy in locally advanced squamous head and neck cancer
Presenter: Juan Carlos Redondo González
Session: Poster session 03
914P - The landscape of somatic copy number alterations of head and neck squamous cell carcinoma across different anatomic sites
Presenter: Juan Carlos Redondo González
Session: Poster session 03
915P - Longer OS and RFS for CD3high/PD-L1+ head and neck squamous cell carcinoma (HNSCC) patients
Presenter: Simon Laban
Session: Poster session 03
916P - Deep spatial profiling of head and neck squamous cell carcinoma offers insights into the tumor microenvironment of hpv-stratified patients
Presenter: Abhishek Aggarwal
Session: Poster session 03