TY - JOUR
T1 - Development and External Validation of a PET Radiomic Model for Prognostication of Head and Neck Cancer
AU - Noortman, Wyanne A.
AU - Aide, Nicolas
AU - Vriens, Dennis
AU - Arkes, Lisa S.
AU - Slump, Cornelis H.
AU - Boellaard, Ronald
AU - Goeman, Jelle J.
AU - Deroose, Christophe M.
AU - Machiels, Jean Pascal
AU - Licitra, Lisa F.
AU - Lhommel, Renaud
AU - Alessi, Alessandra
AU - Woff, Erwin
AU - Goffin, Karolien
AU - Le Tourneau, Christophe
AU - Gal, Jocelyn
AU - Temam, Stéphane
AU - Delord, Jean Pierre
AU - van Velden, Floris H.P.
AU - de Geus-Oei, Lioe Fee
N1 - Funding Information:
Boerhinger Ingelheim France supported the Unicancer Predictor study with treatment supplies and financial funding.
Publisher Copyright:
© 2023 by the authors.
PY - 2023/5
Y1 - 2023/5
N2 - Aim: To build and externally validate an [18F]FDG PET radiomic model to predict overall survival in patients with head and neck squamous cell carcinoma (HNSCC). Methods: Two multicentre datasets of patients with operable HNSCC treated with preoperative afatinib who underwent a baseline and evaluation [18F]FDG PET/CT scan were included (EORTC: n = 20, Unicancer: n = 34). Tumours were delineated, and radiomic features were extracted. Each cohort served once as a training and once as an external validation set for the prediction of overall survival. Supervised feature selection was performed using variable hunting with variable importance, selecting the top two features. A Cox proportional hazards regression model using selected radiomic features and clinical characteristics was fitted on the training dataset and validated in the external validation set. Model performances are expressed by the concordance index (C-index). Results: In both models, the radiomic model surpassed the clinical model with validation C-indices of 0.69 and 0.79 vs. 0.60 and 0.67, respectively. The model that combined the radiomic features and clinical variables performed best, with validation C-indices of 0.71 and 0.82. Conclusion: Although assessed in two small but independent cohorts, an [18F]FDG-PET radiomic signature based on the evaluation scan seems promising for the prediction of overall survival for HNSSC treated with preoperative afatinib. The robustness and clinical applicability of this radiomic signature should be assessed in a larger cohort.
AB - Aim: To build and externally validate an [18F]FDG PET radiomic model to predict overall survival in patients with head and neck squamous cell carcinoma (HNSCC). Methods: Two multicentre datasets of patients with operable HNSCC treated with preoperative afatinib who underwent a baseline and evaluation [18F]FDG PET/CT scan were included (EORTC: n = 20, Unicancer: n = 34). Tumours were delineated, and radiomic features were extracted. Each cohort served once as a training and once as an external validation set for the prediction of overall survival. Supervised feature selection was performed using variable hunting with variable importance, selecting the top two features. A Cox proportional hazards regression model using selected radiomic features and clinical characteristics was fitted on the training dataset and validated in the external validation set. Model performances are expressed by the concordance index (C-index). Results: In both models, the radiomic model surpassed the clinical model with validation C-indices of 0.69 and 0.79 vs. 0.60 and 0.67, respectively. The model that combined the radiomic features and clinical variables performed best, with validation C-indices of 0.71 and 0.82. Conclusion: Although assessed in two small but independent cohorts, an [18F]FDG-PET radiomic signature based on the evaluation scan seems promising for the prediction of overall survival for HNSSC treated with preoperative afatinib. The robustness and clinical applicability of this radiomic signature should be assessed in a larger cohort.
KW - afatinib
KW - head and neck squamous cell carcinoma
KW - machine learning
KW - overall survival
KW - radiomics
KW - [F]FDG PET/CT
UR - http://www.scopus.com/inward/record.url?scp=85160743049&partnerID=8YFLogxK
U2 - 10.3390/cancers15102681
DO - 10.3390/cancers15102681
M3 - Article
AN - SCOPUS:85160743049
SN - 2072-6694
VL - 15
JO - Cancers
JF - Cancers
IS - 10
M1 - 2681
ER -