A1 Refereed original research article in a scientific journal
ENDORISK-2: A personalized Bayesian network for preoperative risk stratification in endometrial cancer, integrating molecular classification and preoperative myometrial invasion assessment
Authors: Lombaers, Marike S.; Reijnen, Casper; Sprik, Ally; Bretová, Petra; Grube, Marcel; Vrede, Stephanie; Berg, Hege F.; Asberger, Jasmin; Colas, Eva; Hausnerova, Jitka; Huvila, Jutta; Gil-Moreno, Antonio; Matias-Guiu, Xavier; Simons, Michiel; Snijders, Marc P. L. M.; Visser, Nicole C. M.; Kommoss, Stefan; Weinberger, Vit; Amant, Frederic; Bronsert, Peter; Haldorsen, Ingfrid S.; Koskas, Martin; Krakstad, Camilla; Küsters-Vandevelde, Heidi V. N.; Mancebo, Gemma; van der Putten, Louis J. M.; de la Calle, Irene; Lucas, Peter J. F.; Hommersom, Arjen; Pijnenborg, Johanna M. A.
Publisher: Pergamon Press
Publication year: 2025
Journal: European Journal of Cancer
Article number: 116058
Volume: 231
ISSN: 0959-8049
eISSN: 1879-0852
DOI: https://doi.org/10.1016/j.ejca.2025.116058
Publication's open availability at the time of reporting: Open Access
Publication channel's open availability : Partially Open Access publication channel
Web address : https://doi.org/10.1016/j.ejca.2025.116058
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/505141979
Background
ENDORISK is a Bayesian network that can assist in preoperative risk estimation of lymph node metastasis (LNM) risk in endometrial cancer (EC) with consistent performance in external validations. To reflect state of the art care, ENDORISK was optimized by integrating molecular classification and preoperative assessment of myometrial invasion (MI).
MethodsVariables for POLE, MSI, and preoperative assessment of MI, either by expert transvaginal ultrasound or pelvic magnetic resonance imaging (MRI), were added to develop ENDORISK-2. The p53 biomarker, part of the molecular classification, was already included in ENDORISK. External validation of ENDORISK-2 for LNM prediction was performed in two independent cohorts from: Brno (CZ), (n = 581) and Tübingen (DE), (n = 247).
FindingsENDORISK-2 yielded AUCs of 0·85 (95 % CI 0·80–0·90) (CZ) and 0·86 (95 % CI 0·77–0·96) (DE) for predicting LNM. In patients with low-grade histology, 83 % (CZ) and 89 % (DE) were estimated having less than 10 % risk of LNM, with false negative rates (FNR) of 4·3 % (CZ) and 2·2 % (DE). The previously defined set of minimally required variables, i.e.: preoperative tumor grade, three of the four immunohistochemical (IHC) markers, and one clinical marker, could be interchanged with the new variables, with comparable validation metrics, including AUC values of 0·79–0·87 for LNM prediction.
Interpretation. Incorporation of molecular data and preoperative MI improved the flexibility of ENDORISK with comparable diagnostic accuracy for estimating LNM as when based on low-cost immunohistochemical biomarkers. In addition, the high diagnostic accuracy in patients with low-grade EC demonstrates how ENDORISK-2 could aid clinicians in identifying patients in whom surgical lymph node assessment may safely be omitted. These results underline its power for clinical use in both high and low resource countries.
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Funding information in the publication:
This study was funded by the Dutch Cancer society (KWF-10616).