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
1015P - The efficacy and mechanism of pan-FGFR inhibitor (AZD4547) combined with immunoagonists or immunosuppressants in FGFR-positive tumors
Presenter: Qizhi Ma
Session: Poster session 03
1016P - Phase I study of SOF10 plus atezolizumab in patients with advanced/recurrent solid tumours
Presenter: Toshihiko Doi
Session: Poster session 03
1017P - Updated safety and efficacy from the phase I study of givastomig, a novel claudin 18.2/4-1BB bispecific antibody, in claudin 18.2 positive advanced gastroesophageal carcinoma (GEC)
Presenter: Samuel Klempner
Session: Poster session 03
1018P - Leveraging innate and adaptive immunity with AFM24 and atezolizumab in metastatic gastric cancer
Presenter: Omar Saavedra Santa Gadea
Session: Poster session 03
1019P - Bispecific PD1-IL2 antibody reshapes the inhibitory immune microenvironment of SMARCA4 mutant non-small cell lung cancer by reversing CD8+T cell exhaustion
Presenter: Bo Cheng
Session: Poster session 03
Resources:
Abstract
1020P - Highly potent and specific bivalent T cell engager (TCE) targeting PRAME on HLA-A*02:01
Presenter: Athanasia Dasargyri
Session: Poster session 03
1021P - Chemotherapy and hypomethylating agents enhance anti-tumor activity of PRAME ImmTAC
Presenter: Adel Benlahrech
Session: Poster session 03
1022P - A phase II trial of the IO102-IO103 vaccine plus pembrolizumab: Completed cohort for first-line (1L) treatment of advanced squamous cell carcinoma of the head and neck (SCCHN)
Presenter: Jonathan Riess
Session: Poster session 03
1023P - Long-term follow up of patients treated with a DNA vaccine (pTVG-HP) for PSA-recurrent prostate cancer
Presenter: Douglas McNeel
Session: Poster session 03
1024P - Initial clinical results of BT-001, an oncolytic virus expressing an anti-CTLA4 mAb, administered as single agent and in combination with pembrolizumab in patients with advanced solid tumors
Presenter: Stephane Champiat
Session: Poster session 03