2025
ENDORISK-2: A personalized Bayesian network for preoperative risk stratification in endometrial cancer, integrating molecular classification and preoperative myometrial invasion assessment
LOMBAERS, Marike S; Casper REIJNEN; Ally SPRIK; Petra BRETOVÁ; Marcel GRUBE et al.Základní údaje
Originální název
ENDORISK-2: A personalized Bayesian network for preoperative risk stratification in endometrial cancer, integrating molecular classification and preoperative myometrial invasion assessment
Autoři
LOMBAERS, Marike S; Casper REIJNEN; Ally SPRIK; Petra BRETOVÁ; Marcel GRUBE; Stephanie VREDE; Hege F BERG; Jasmin ASBERGER; Eva COLAS; Jitka HAUSNEROVÁ; Jutta HUVILA; Antonio GIL-MORENO; Xavier MATIAS-GUIU; Michiel SIMONS; Marc P L M SNIJDERS; Nicole C M VISSER; Stefan KOMMOSS; Vít WEINBERGER; Frederic AMANT; Peter BRONSERT; Ingfrid S HALDORSEN; Martin KOSKAS; Camilla KRAKSTAD; Heidi V N KUSTERS-VANDEVELDE; Gemma MANCEBO; Louis J M VAN DER PUTTEN; De La Calle IRENE; Peter J F LUCAS; Arjen HOMMERSOM a Johanna M A PIJNENBORG
Vydání
European Journal of Cancer, London, ELSEVIER, 2025, 0959-8049
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30204 Oncology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 7.100 v roce 2024
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/25:00142810
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Endometrial cancer; Risk estimation; Lymph node metastasis; Bayesian network; Molecular classification; Myometrial invasion
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 4. 12. 2025 12:59, Mgr. Tereza Miškechová
Anotace
V originále
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). Methods: Variables 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 pre-diction was performed in two independent cohorts from: Brno (CZ), (n = 581) and T & uuml;bingen (DE), (n = 247). Findings: ENDORISK-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 bio-markers. 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.