Abstract 1413P
Background
The surveillance protocol for early-stage esophageal cancer is not contingent upon individualized risk factors for recurrence. This study aimed to develop a deep-learning model using comprehensive data from clinical practice for practical longitudinal monitoring.
Methods
A multi-modal deep-learning model employing transformers was developed for real-time recurrence prediction using clinical, pathological, and molecular data at baseline, alongside longitudinal laboratory, and radiologic data during surveillance. Patients with histologically confirmed esophageal cancer (stage I-III) undergoing curative intent surgery between January 2008 and September 2022 were included. The collected data was divided into training and validation in a 5:5 ratio. The primary outcome focused on predicting likelihood of recurrence within one year from the monitoring point. This study demonstrated the timely provision of risk scores (RADAR score), determined thresholds, and the corresponding Area Under the Curve (AUC).
Results
A total of 1,486 patients were enrolled (655 with stage I, 457 with stage II, and 374 with stage III). The training and validation sets comprised 743 and 743 patients, respectively. The model incorporated 9 clinical-pathological-molecular factors at baseline, alongside longitudinal laboratory, and radiologic text data. Radiologic data of 11,933 was used (mean 8.0 chest CT scan per patient) during surveillance. Baseline RADAR score wsa 0.257 (standard deviation [Std] 0.132) in stage I, 0.468 (Std 0.116) in stage II, and 0.684 (Std 0.107) in stage III. The AUC for predicting relapse within one year from that monitoring point was 0.795 across all stages with the sensitivity of 77.2% and specificity of 70.1% (AUC=0.774 in stage I, AUC=0.697 in stage II, and AUC=0.683 in stage III).
Conclusions
This pilot study introduces a deep-learning model utilizing multi-modal data from routine clinical practice for predicting relapse in early-stage esophageal cancer. It demonstrates the timely provision of risk score, RADAR score, to clinicians for recurrence prediction, potentially guiding risk- adapted surveillance strategies and aggressive adjuvant systemic treatment.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1154P - Prospective multinational evaluation of alkylating-induced hypermutation in neuroendocrine neoplasms (NEN): Clinical and molecular profiles associated with response to immune checkpoint inhibitors (CPI)
Presenter: Elena Trevisani
Session: Poster session 17
1156P - The efficacy of lower doses of everolimus in patients with advanced neuroendocrine tumors
Presenter: Rachel Riechelmann
Session: Poster session 17
1157P - Retreatment with peptide receptor radionuclide therapy (PRRT) in patients (p) with neuroendocrine tumors (NET): Spanish clinical experience from SEPTRALU national registry
Presenter: Jorge Hernando Cubero
Session: Poster session 17
1158P - A novel nomogram for predicting overall survival of small intestinal neuroendocrine tumors treated with PRRT
Presenter: Dimitrios Papantoniou
Session: Poster session 17
1159P - Molecular characterization of extra-pulmonary mixed adeno-neuroendocrine carcinomas: The NIRVANA substudy
Presenter: Francesca Spada
Session: Poster session 17
1160P - An Italian multicenter phase II trial of metronomic temozolomide in unfit patients with advanced neuroendocrine neoplasms: Interim analysis of the MeTe study
Presenter: Francesca Spada
Session: Poster session 17
1161P - Progression-free survival ratio and the implications for treatment sequencing in neuroendocrine neoplasms
Presenter: Philipp Melhorn
Session: Poster session 17
1162P - Transcriptomic analysis of gastroenteropancreatic neuroendocrine tumours with carcinoid syndrome
Presenter: Javier Pozas Perez
Session: Poster session 17
1163P - Prognostic value of systemic inflammatory index (SII) in neuroendocrine tumors (NETs) treated with peptide receptor radionuclide therapy (PRRT)
Presenter: Eduardo Terán Brage
Session: Poster session 17