Improving preoperative diagnosis in endometrial cancer using systematic morphological assessment and a small immunohistochemical panel.


Journal

Human pathology
ISSN: 1532-8392
Titre abrégé: Hum Pathol
Pays: United States
ID NLM: 9421547

Informations de publication

Date de publication:
11 2021
Historique:
received: 30 05 2021
revised: 22 07 2021
accepted: 12 08 2021
pubmed: 22 8 2021
medline: 24 12 2021
entrez: 21 8 2021
Statut: ppublish

Résumé

Preoperative histopathological classification determines the primary surgical approach in endometrial carcinoma (EC) patients but has only moderate agreement between preoperative and postoperative diagnosis. The aim of the PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study is to determine whether histopathological assessment and a small panel of diagnostic biomarkers decreases discrepancies between preoperative and postoperative diagnosis in EC. Preoperative endometrial tissue of 378 included patients with EC was stained with 15 different antibodies. Clinically relevant discrepancies in grade or histological subtype between original preoperative and reviewed postoperative diagnosis were observed in 75 (20%) patients. Highest clinically relevant discrepancy was found in grade 2 ECs (20%), compared to 5% and 14% in respectively grade 1 and 3 endometrioid endometrial carcinomas (EECs). A practical two-biomarker panel with PR and p53 improved diagnostic accuracy (AUC = 0.92; 95%CI = 0.88-0.95) compared to solely morphological evaluation (AUC = 0.86). In preoperative high-grade EC, the diagnostic accuracy of histological subtype was improved by a three-immunohistochemical biomarker panel (PR, IMP3, and L1CAM) (AUC = 0.93; 95%CI = 0.88-0.98) compared to solely morphological evaluation (AUC = 0.81). In conclusion to improve correct preoperative diagnosis in EC, we recommend use of a panel of at least two easily accessible immunohistochemical biomarkers (PR and p53), only in grade 2 ECs. Overall, this will reduce clinically relevant discrepancies in tumor grade and subtype with postoperative diagnosis with 6% (from 20% to 14%). Addition of PR, IMP3, and L1CAM for histological subtyping in high-grade EECs resulted in a further decrease in discrepancies with 8% (from 20% to 12%).

Identifiants

pubmed: 34418427
pii: S0046-8177(21)00148-9
doi: 10.1016/j.humpath.2021.08.006
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
IMP3 protein, human 0
L1CAM protein, human 0
Neural Cell Adhesion Molecule L1 0
Receptors, Progesterone 0
Ribonucleoproteins, Small Nucleolar 0
TP53 protein, human 0
Tumor Suppressor Protein p53 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

68-78

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Nicole C M Visser (NCM)

Dept. Pathology, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands; Dept. Pathology, Stichting PAMM, 5623 EJ, Eindhoven, the Netherlands. Electronic address: n.visser@pamm.nl.

Anneke A M van der Wurff (AAM)

Dept. Pathology, Elisabeth-TweeSteden Hospital, 5000 LC, Tilburg, the Netherlands.

Joanna IntHout (J)

Dept. for Health Evidence, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands.

Casper Reijnen (C)

Dept. Radiation Oncology, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands; Dept. Obstetrics and Gynecology, Canisius Wilhelmina Hospital, 6500 GS, Nijmegen, the Netherlands.

Parag D Dabir (PD)

Dept. Pathology, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands; Dept. Pathology, Regional Hospital, 8930, Randers, Denmark.

Gilda G Soltani (GG)

Dept. Pathology, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands.

Luthy S M Alcala (LSM)

Dept. Pathology, Amphia Hospital, 4800 RL, Breda, the Netherlands.

Dorry Boll (D)

Dept. Gynecology, Catharina Hospital, 5623 EJ, Eindhoven, the Netherlands.

Carolien M Bronkhorst (CM)

Dept. Pathology, Jeroen Bosch Hospital, 5200 ME, 's-Hertogenbosch, the Netherlands.

Peter Bult (P)

Dept. Pathology, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands.

Peggy M A J Geomini (PMAJ)

Dept. Obstetrics and Gynecology, Maxima Medical Centre, 5504 DB, Veldhoven and Eindhoven, the Netherlands.

Dennis van Hamont (D)

Dept. Obstetrics and Gynecology, Amphia Hospital, 4800 RL, Breda, the Netherlands.

Hilde A D M van Herk (HADM)

Dept. Pathology, Stichting PAMM, 5623 EJ, Eindhoven, the Netherlands.

Ineke M de Kievit (IM)

Dept. Pathology, Canisius Wilhelmina Hospital, 6500 GS, Nijmegen, the Netherlands.

Huy Ngo (H)

Dept. Obstetrics and Gynecology, Elkerliek Hospital, 5700AB, Helmond, the Netherlands.

Brenda M Pijlman (BM)

Dept. Obstetrics and Gynecology, Jeroen Bosch Hospital, 5200 ME, 's-Hertogenbosch, the Netherlands.

Marc P M L Snijders (MPML)

Dept. Obstetrics and Gynecology, Canisius Wilhelmina Hospital, 6500 GS, Nijmegen, the Netherlands.

M Caroline Vos (MC)

Dept. Obstetrics and Gynecology, Elisabeth-TweeSteden Hospital, 5000 LC, Tilburg, the Netherlands.

Iris D Nagtegaal (ID)

Dept. Pathology, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands.

Leon F A G Massuger (LFAG)

Dept. Obstetrics and Gynecology, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands.

Johanna M A Pijnenborg (JMA)

Dept. Obstetrics and Gynecology, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands.

Johan Bulten (J)

Dept. Pathology, Radboud University Medical Center, 6500 HB, Nijmegen, the Netherlands.

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Classifications MeSH