Application of novel algorithm on a retrospective series to implement the molecular classification for endometrial cancer.

Author:

Arcieri Martina1,Occhiali Tommaso2,Giorgiutti Cristina2,Tius Veronica2,Pregnolato Sara2,Mariuzzi Laura2,Orsaria Maria3,Andreetta Claudia4,Titone Francesca5,Damante Giuseppe2,D'Elia Angela Valentina6,Biasioli Anna1,Martina Monica Della1,Fanfani Francesco7,Ercoli Alfredo8,Driul Lorenza1,Scambia Giovanni7,Vizzielli Giuseppe1,Restaino Stefano1

Affiliation:

1. Department of Maternal and Child Health, Obstetrics and Gynecology Clinic, University Hospital of Udine, Udine, Italy

2. Medical Area Department (DAME), University of Udine, Udine, Italy

3. Institute of Pathology, University Hospital of Udine, Udine, Italy

4. Oncology Department, University Hospital of Udine, Udine, Italy

5. Department of Radiation Oncology, University Hospital Udine, Udine, Italy

6. Institute of Medical Genetics, University Hospital of Udine, Udine, Italy

7. Department of Woman, Child, and Public Health, Fondazione Policlinico Universitario A. Gemelli Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy

8. Department of Human Pathology of Adult and Childhood "G. Barresi", Unit of Gynecology and Obstetrics, University of Messina, Messina, Italy

Abstract

Abstract Background The study aimed to validate the Betella algorithm, focusing on molecular analyses exclusively for endometrial cancer patients, where molecular classification alters risk assessment based on ESGO/ESTRO/ESP 2020 guidelines. Methods Conducted between March 2021 and March 2023, the retrospective research involved endometrial cancer patients undergoing surgery and comprehensive molecular analyses. These included p53 and mismatch repair proteins immunohistochemistry, as well as DNA sequencing for POLE exonuclease domain. We applied the Betella alghoritm to our population and evaluated the proportion of patients in which the molecular analysis changed the risk class attribution. Results Among 102 patients, 97% obtained complete molecular analyses. The cohort exhibited varying molecular classifications: 10.1% as POLE ultra-mutated, 30.3% as mismatch repair deficient, 11.1% as p53 abnormal, and 48.5% as non-specified molecular classification. Multiple classifiers were present in 3% of cases. Integrating molecular classification into risk group calculation led to risk group migration in 11.1% of patients: 7 moved to lower risk classes due to POLE mutations, while 4 shifted to higher risk due to p53 alterations. Applying Betella algorithm, we can spare the POLE sequencing in 65 cases (65.7%) and p53 immunochemistry in 17 cases (17.2%). Conclusion The application of this new proposed algorithm appears safe for the patients while rationalizing resources that could be otherwise allocated, making it not only useful for low resources settings, but for all settings in general.

Publisher

Research Square Platform LLC

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