Abstract 934P
Background
Almost half of patients with early/locally advanced (LA) head and neck squamous cell carcinoma (HNSCC) progress or relapse within 2 years. We applied artificial intelligence (AI) techniques to extract clinical variables from electronic health records (EHR) and to predict treatment failure.
Methods
This is an international, observational, retrospective study using free-text and structured data from HNSCC patients’ EHRs. A total of 203 clinical variables were extracted running EHRead®, a multilingual natural language processing (NLP) engine employing SNOMED-CT, from the EHR’s of HNSCC patients from 6 hospitals from Spain, France, and Colombia (2014-2021). Only patients with incident early/LA HNSCC were included. We utilized machine learning to train and 10-fold-cross validate several algorithms to predict progression, recurrence, or death within 2 years after radical treatment, selecting the model with the best performance metrics.
Results
Among 2,034,994 patients screened, 1,209 individuals were identified with early (44%) and LA (56%) HNSCC: 39.7% oral cavity, 32.8% larynx, 23.1% oropharynx, and 4.5% hypopharynx. Median age was 65 years (69.2% male). Main comorbidities were hypertension (50.1%), diabetes (33.3%). Most frequent symptoms at diagnosis were pain (60.7%), dysphagia (25.6%). A total of 484 (40%) patients experienced progression, recurrence, or death within 2 years. The algorithm with the best performance to predict radical treatment failure employed a random forest model, with an area under the ROC curve of 0.709. The main predictors of this model were: Age, stage, alcohol consumption, involved nodes, pain at diagnosis and surgical treatment.
Conclusions
This first phase of the HNC-TACTIC study shows the ability of NLP to extract accurate clinical data from HNSCC patients’ EHRs, and for machine-learning models to predict risk of treatment failure, demonstrating the potential capabilities of AI-powered real-world studies. The next phase will validate and retrain this model on data from 9 countries.
Clinical trial identification
NCT05117775.
Editorial acknowledgement
Legal entity responsible for the study
Savana S.L.
Funding
Savana S. L.
Disclosure
M. López, E. Castillo: Financial Interests, Institutional, Full or part-time Employment: Savana S. L. L. Cabal Hierro: Non-Financial Interests, Institutional, Full or part-time Employment: Savana S. L. H.T. Study Group: Financial Interests, Institutional, Full or part-time Employment, Judith Marín-Corral, Bianca de León, Ignacio Salcedo, David Casadevall, Victor Fanjul, Sebastian Menke, Almudena Chapa, Adrián Ceja: Savana S. L. ; Non-Financial Interests, Institutional, Affiliate, John de Almeida (UHN Canada), Andreas Dietz (Leipzig, Germany), Robert Ferris (UPMC, USA, Raul Giglio (Hospital Roffo, Argentina), Chris Holsinger (Stanford University School of Medicine, USA), Kate Hutcheson (MD Anderson Cancer Center, USA), Sandro Porceddu (Queensland Health, Australia), Christian Simon (Lausanne University Hospital, Switzerland), Ana López Alfonso (HUIL, Spain), Gloria María Serrano Montero (HUIL, Spain), Laura Rodrigáñez Riesco (H La Paz, Spain), Beatriz Castelo Fernández (H La Paz, Spain), Cristina Urbano (H de Granollers, Spain), Jordi Serra Carreras (H Granollers, Spain), Carlos García (H Alma Matter de Antioquia, Colombia), Yair Monsalve (H Alma Matter de Antioquia, Colombia), Javier Alonso Ortega (H de Móstoles, Spain), Gabriela Morales Medina (H de Móstoles, Spain), Renaud Schiappa (Centre Antoine Lacassagne, France,: Savana S. L. M. Taberna: Financial Interests, Institutional, Full or part-time Employment: Savana S. L. All other authors have declared no conflicts of interest.
Resources from the same session
1025P - Fully intravenous delivery regimen of oncolytic adenovirus coding for TNFa and IL-2 (TILT-123) in patients with advanced solid cancers
Presenter: Santeri Pakola
Session: Poster session 03
1026P - Updated results from the phase I 1456-0001 study for intratumoral (IT) VSV-GP (BI 1831169) in patients with advanced solid tumors
Presenter: Stephane Champiat
Session: Poster session 03
1027P - First results for intravenous (IV) VSV-GP (BI 1831169) in patients (pts) with advanced solid tumors from the 1456-0001 study
Presenter: Marc Oliva Bernal
Session: Poster session 03
1028P - A phase I study of personalized KSX01-TCRT therapy for advanced solid tumor and its mechanisms
Presenter: Shuhang Wang
Session: Poster session 03
Resources:
Abstract
1029P - Preclinical development of TCR-modified T cell therapies against mutated KRAS
Presenter: Hugh Salter
Session: Poster session 03
1030P - Survival rates in high-risk neuroblastoma patients undergoing anti-GD2 immunotherapy: A single arm meta-analysis and systemic review
Presenter: Lorena Escalante Romero
Session: Poster session 03
1032P - Tumor-infiltrating lymphocytes with inducible membrane-tethered IL-12 cultured in optimized media exhibits superior anti-tumor activity
Presenter: Patrick Innamarato
Session: Poster session 03
1033P - Anti-tumor efficacy and safety of conditionally activated armored CAR-T cells against gastrointestinal tumors
Presenter: Zhihong Huang
Session: Poster session 03
1034P - Preclinical development of genetically modified tumor-infiltrating lymphocytes using biopsy samples from liver cancer patients
Presenter: Mingyu Liu
Session: Poster session 03
1035P - A new IL-6 inducing mechanism in cancer with new therapeutic possibilities
Presenter: Leif Håkansson
Session: Poster session 03