Correlation between P53 immunohistochemical staining and <i>TP53</i> molecular testing in endometrial carcinomas: a detailed assessment of discrepant cases with implications for patient management

Our study demonstrated a good overall concordance between p53 immunohistochemical staining and TP53 molecular results. The concordance can be increased by reviewing the p53 stained slides in discrepant cases but there remains a small cohort of cases, mostly low-grade endometrioid carcinomas (POLE wild-type/MMR proficient), where TP53 mutations are present on NGS but p53 immunohistochemistry is wild-type. Such cases present a dilemma for the pathologist (which TCGA group should they be placed into) and the clinician (should adjuvant therapy be instigated based on the presence of a TP53 mutation alone with no other adverse features). For now, we advise classifying such cases as p53abn but not to administer adjuvant therapy based on the presence of a TP53 mutation alone without other adverse pathological factors. The significance of TP53 mutations in such cases should be determined by larger studies with long-term follow-up.

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Publication Details

Journal
Histopathology
Published
2025-10-31
DOI
https://doi.org/10.1111/his.70029
Primary Topic
Endometrial and Cervical Cancer Treatments
Type
article
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article

Correlation between P53 immunohistochemical staining and TP53 molecular testing in endometrial carcinomas: a detailed assessment of discrepant cases with implications for patient management

W. Glenn McCluggage, Jesús Machuca‐Aguado, Mark Catherwood, David González
Histopathology
Endometrial and Cervical Cancer Treatments
article

Correlation between P53 immunohistochemical staining and TP53 molecular testing in endometrial carcinomas: a detailed assessment of discrepant cases with implications for patient management

W. Glenn McCluggage, Jesús Machuca‐Aguado, Mark Catherwood, David González
article en

Abstract

Our study demonstrated a good overall concordance between p53 immunohistochemical staining and TP53 molecular results. The concordance can be increased by reviewing the p53 stained slides in discrepant cases but there remains a small cohort of cases, mostly low-grade endometrioid carcinomas (POLE wild-type/MMR proficient), where TP53 mutations are present on NGS but p53 immunohistochemistry is wild-type. Such cases present a dilemma for the pathologist (which TCGA group should they be placed into) and the clinician (should adjuvant therapy be instigated based on the presence of a TP53 mutation alone with no other adverse features). For now, we advise classifying such cases as p53abn but not to administer adjuvant therapy based on the presence of a TP53 mutation alone without other adverse pathological factors. The significance of TP53 mutations in such cases should be determined by larger studies with long-term follow-up.

HistopathologyVol. 88(3)
Queen's University Belfast (GB), Belfast Health and Social Care Trust (GB), Hospital Universitario Virgen Macarena (ES), Universidad de Sevilla (ES)
Openalex Percentile: Top 60%
Endometrial and Cervical Cancer Treatments
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