Hormone Receptor Expression and Activity for Different Tumour Locations in Patients with Advanced and Recurrent Endometrial Carcinoma.

endometrial cancer hormone receptor tumour location

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
30 May 2024
Historique:
received: 15 04 2024
revised: 10 05 2024
accepted: 23 05 2024
medline: 19 6 2024
pubmed: 19 6 2024
entrez: 19 6 2024
Statut: epublish

Résumé

Response to hormonal therapy in advanced and recurrent endometrial cancer (EC) can be predicted by oestrogen and progesterone receptor immunohistochemical (ER/PR-IHC) expression, with response rates of 60% in PR-IHC > 50% cases. ER/PR-IHC can vary by tumour location and is frequently lost with tumour progression. Therefore, we explored the relationship between ER/PR-IHC expression and tumour location in EC. Pre-treatment tumour biopsies from 6 different sites of 80 cases treated with hormonal therapy were analysed for ER/PR-IHC expression and classified into categories 0-10%, 10-50%, and >50%. The ER pathway activity score (ERPAS) was determined based on mRNA levels of ER-related target genes, reflecting the actual activity of the ER receptor. There was a trend towards lower PR-IHC (33% had PR > 50%) and ERPAS (27% had ERPAS > 15) in lymphogenic metastases compared to other locations ( A trend towards lower PR-IHC and ERPAS was observed in lymphogenic sites. Verification in larger cohorts is needed to confirm these findings, which may have implications for the use of hormonal therapy in the future.

Sections du résumé

BACKGROUND BACKGROUND
Response to hormonal therapy in advanced and recurrent endometrial cancer (EC) can be predicted by oestrogen and progesterone receptor immunohistochemical (ER/PR-IHC) expression, with response rates of 60% in PR-IHC > 50% cases. ER/PR-IHC can vary by tumour location and is frequently lost with tumour progression. Therefore, we explored the relationship between ER/PR-IHC expression and tumour location in EC.
METHODS METHODS
Pre-treatment tumour biopsies from 6 different sites of 80 cases treated with hormonal therapy were analysed for ER/PR-IHC expression and classified into categories 0-10%, 10-50%, and >50%. The ER pathway activity score (ERPAS) was determined based on mRNA levels of ER-related target genes, reflecting the actual activity of the ER receptor.
RESULTS RESULTS
There was a trend towards lower PR-IHC (33% had PR > 50%) and ERPAS (27% had ERPAS > 15) in lymphogenic metastases compared to other locations (
CONCLUSIONS CONCLUSIONS
A trend towards lower PR-IHC and ERPAS was observed in lymphogenic sites. Verification in larger cohorts is needed to confirm these findings, which may have implications for the use of hormonal therapy in the future.

Identifiants

pubmed: 38893205
pii: cancers16112084
doi: 10.3390/cancers16112084
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Maartje M W Luijten (MMW)

Department of Obstetrics and Gynaecology, Radboud University Medical Centre, 6525 GA Nijmegen, The Netherlands.
Department of Gynaecology, Rijnstate Hospital, 6815 AD Arnhem, The Netherlands.

Willem Jan van Weelden (WJ)

Department of Obstetrics and Gynaecology, Radboud University Medical Centre, 6525 GA Nijmegen, The Netherlands.
Department of Obstetrics and Gynaecology, Canisius Wilhelmina Hospital, 6532 SZ Nijmegen, The Netherlands.

Roy I Lalisang (RI)

GROW-School of Oncology and Developmental Biology, Maastricht University Medical Center+, 6229 ER Maastricht, The Netherlands.

Johan Bulten (J)

Department of Pathology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.

Kristina Lindemann (K)

Division of Medicine, Department of Gynecological Oncology, Oslo University Hospital, 0424 Oslo, Norway.
Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, 0372 Oslo, Norway.

Heleen J van Beekhuizen (HJ)

Department of Gynecologic Oncology, Erasmus MC Cancer Institute, Erasmus Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands.

Hans Trum (H)

Center for Gynecologic Oncology Amsterdam, Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.

Dorry Boll (D)

Department of Gynaecology, Catharina Hospital, 5623 EJ Eindhoven, The Netherlands.

Henrica M J Werner (HMJ)

Department of Obstetrics and Gynecology, Maastricht University Medical Center+, 6229 HX Maastricht, The Netherlands.

Luc R C W van Lonkhuijzen (LRCW)

Department of Gynaecology and Obstetrics, Amsterdam University Medical Centers, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.

Refika Yigit (R)

Department of Obstetrics and Gynecology, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.

Camilla Krakstad (C)

Department of Gynecology and Obstetrics, Haukeland University Hospital, 5009 Bergen, Norway.

Petronella O Witteveen (PO)

Department of Medical Oncology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.

Khadra Galaal (K)

Sultan Qaboos Comprehensive Cancer Center, Muscat P.O. Box 566 PC 123, Oman.

Alexandra A van Ginkel (AA)

Department of Gynaecology, Rijnstate Hospital, 6815 AD Arnhem, The Netherlands.

Eliana Bignotti (E)

Division of Obstetrics and Gynecology, A. Nocivelli Institute for Molecular Medicine, ASST Spedali Civili di Brescia, 25123 Brescia, Italy.

Vit Weinberger (V)

Department of Obstetrics and Gynecology, Faculty of Medicine, Masaryk University, 625 00 Brno, Czech Republic.
Department of Obstetrics and Gynecology, University Hospital Brno, 625 00 Brno, Czech Republic.

Sanne Sweegers (S)

Department of Obstetrics and Gynaecology, Radboud University Medical Centre, 6525 GA Nijmegen, The Netherlands.

Ane Gerda Z Eriksson (AGZ)

Division of Medicine, Department of Gynecological Oncology, Oslo University Hospital, 0424 Oslo, Norway.
Faculty of Medicine, Institute of Clinical Medicine, University of Oslo, 0372 Oslo, Norway.

Diederick M Keizer (DM)

InnoSIGN, 5656 AE Eindhoven, The Netherlands.

Anja van de Stolpe (A)

DCDC-Tx B.V., 5263 EM Vught, The Netherlands.

Andrea Romano (A)

GROW-School of Oncology and Developmental Biology, Maastricht University Medical Center+, 6229 ER Maastricht, The Netherlands.
Department of Obstetrics and Gynecology, Maastricht University Medical Center+, 6229 HX Maastricht, The Netherlands.

Johanna M A Pijnenborg (JMA)

Department of Obstetrics and Gynaecology, Radboud University Medical Centre, 6525 GA Nijmegen, The Netherlands.

Classifications MeSH