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Endometrial Carcinosarcomas are Almost Exclusively of p53abn Molecular Subtype After Exclusion of Mimics




TekijätHuvila, Jutta; Jamieson, Amy; Pors, Jennifer; Hoang, Lynn; Mirkovic, Jelena; Cochrane, Dawn; McAlpine, Jessica N.; Gilks, C. Blake

KustantajaLIPPINCOTT WILLIAMS & WILKINS

KustannuspaikkaPHILADELPHIA

Julkaisuvuosi2024

JournalInternational Journal of Gynecologic Pathology

Tietokannassa oleva lehden nimiINTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY

Lehden akronyymiINT J GYNECOL PATHOL

Vuosikerta43

Numero5

Aloitussivu506

Lopetussivu514

Sivujen määrä9

ISSN0277-1691

eISSN1538-7151

DOIhttps://doi.org/10.1097/PGP.0000000000001010

Verkko-osoitehttps://doi.org/10.1097/PGP.0000000000001010

Rinnakkaistallenteen osoitehttps://pmc.ncbi.nlm.nih.gov/articles/PMC11771344/


Tiivistelmä
Our aim was to assess the molecular subtype(s) and perform a detailed morphologic review of tumors diagnosed as carcinosarcoma in a population-based cohort. Forty-one carcinosarcomas were identified from a cohort of 973 endometrial carcinomas diagnosed in 2016. We assessed immunostaining and sequencing data and undertook expert pathology reviews of these cases as well as all subsequently diagnosed (post-2016) carcinosarcomas of no specific molecular profile (NSMP) molecular subtype (n=3) from our institutions. In the 2016 cohort, 37 of the 41 carcinosarcomas (91.2%) were p53abn, 2 (4.9%) were NSMP, and 1 each (2.4%) were POLEmut and mismatch repair deficiency molecular subtypes, respectively. Of the 4 non-p53abn tumors on review, both NSMP tumors were corded and hyalinized (CHEC) pattern endometrioid carcinoma, the mismatch repair deficiency tumor was a grade 1 endometrioid carcinoma with reactive stromal proliferation, and the POLEmut tumor was grade 3 endometrioid carcinoma with spindle cell growth, that is, none were confirmed to be carcinosarcoma on review. We found 11 additional cases among the 37 p53abn tumors that were not confirmed to be carcinosarcoma on the review (3 undifferentiated or dedifferentiated carcinomas, 5 carcinomas with CHEC features, 2 carcinomas showing prominent reactive spindle cell stroma, and 1 adenosarcoma). In the review of institutional cases reported as NSMP carcinosarcoma after 2016, 3 were identified (1 adenosarcoma and 2 mesonephric-like adenocarcinoma on review). In this series, all confirmed endometrial carcinosarcomas were p53abn. The finding of any other molecular subtype in a carcinosarcoma warrants pathology review to exclude mimics.


Julkaisussa olevat rahoitustiedot
This work was funded by the Canadian Cancer Society Uterine Carcinosarcoma and Aggressive Uterine Cancer Research Grant (#707034), the Michael Smith Health Research BC Innovation to Commercialization Award and the Terry Fox Research Institute Program Project Grant. This team has also been supported through funding from the Canada Research Chairs Program (JMc), the BC Cancer Foundation (Clinician Scientist Award (JMc)), the Chew Wei Memorial Chair in Gynecologic Oncology (JMc), the Vancouver Coastal Health Research Institute (Mentored Clinician Scientist Investigator Award (AJ)), and the Miller Mindell Fellowship (AJ) through the VGH & UBC Hospital Foundation.


Last updated on 2025-21-03 at 11:31