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Prognosis of Stage I Endometrial Cancer According to the FIGO 2023 Classification Taking into Account Molecular Changes.
Dobrzycka, Bozena; Terlikowska, Katarzyna Maria; Kowalczuk, Oksana; Niklinski, Jacek; Kinalski, Maciej; Terlikowski, Slawomir Jerzy.
Afiliação
  • Dobrzycka B; Department of Gynecology and Practical Obstetrics, Medical University of Bialystok, 15-295 Bialystok, Poland.
  • Terlikowska KM; Department of Food Biotechnology, Medical University of Bialystok, 15-295 Bialystok, Poland.
  • Kowalczuk O; Department of Clinical Molecular Biology, Medical University of Bialystok, 15-269 Bialystok, Poland.
  • Niklinski J; Department of Clinical Molecular Biology, Medical University of Bialystok, 15-269 Bialystok, Poland.
  • Kinalski M; Department of Gynecology and Obstetrics, Independent Public Healthcare Facility Regional Complex Jan Sniadecki Hospital in Bialystok, 15-595 Bialystok, Poland.
  • Terlikowski SJ; Department of Obstetrics, Gynecology and Maternity Care, Medical University of Bialystok, 15-295 Bialystok, Poland.
Cancers (Basel) ; 16(2)2024 Jan 17.
Article em En | MEDLINE | ID: mdl-38254879
ABSTRACT
Optimum risk stratification in an early stage of endometrial cancer (EC) combines molecular and clinicopathological features. The purpose of the study was to determine the prognostic value of molecular classification and traditional pathological factors in a sample group of patients with stage I EC according to the FIGO 2023 criteria, to achieve a more personalized approach to patient care and treatment. The immunohistochemistry for p53 and mismatch repair (MMR) proteins, and DNA sequencing for POLE exonuclease domain and clinicopathological parameters, including disease disease-free survival (DFS) and overall survival (OS) in 139 patients, were analyzed. It has been shown that the independent recurrence risk factors are stage IC (p < 0.001), aggressive histological types EC (p < 0.001), and the presence of p53abn protein immunoexpression (p = 0.009). Stage IC (p = 0.018), aggressive histological types EC (p = 0.025) and the presence of p53abn protein immunoexpression (p = 0.010) were all significantly associated with lower 5-year OS rates. Our research studies confirm that the molecular category corresponds to a different prognosis in clinical stage I EC according to the new 2023 FIGO classification, with POLEmut cases presenting the best outcomes and p53abn cases showing the worst outcomes. Beyond the previous routine clinicopathological assessment, the new EC staging system represents an important step toward improving our ability to stratify IC stage EC risk.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2024 Tipo de documento: Article