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Authors

Martin Köbel
Eun-Young Kang
Ashley Weir
Peter F Rambau
Cheng-Han Lee
Gregg S Nelson
Prafull Ghatage
Nicola S Meagher
Marjorie J Riggan
Jennifer Alsop
Michael S Anglesio
Matthias W Beckmann
Christiani Bisinotto
Michelle Boisen
Jessica Boros
Alison H Brand
Angela Brooks-Wilson
Michael E Carney
Penny Coulson
Madeleine Courtney-Brooks
Kara L Cushing-Haugen
Cezary Cybulski
Suha Deen
Mona A El-Bahrawy
Esther Elishaev
Ramona Erber
Sian Fereday
AOCS Group
Anna Fischer
Simon A Gayther
Arantzazu Barquin-Garcia
Aleksandra Gentry-Maharaj
C Blake Gilks
Helena Gronwald
Marcel Grube
Paul R Harnett
Holly R Harris
Andreas D Hartkopf
Arndt Hartmann
Alexander Hein
Joy Hendley
Brenda Y Hernandez
Yajue Huang
Anna Jakubowska
Mercedes Jimenez-Linan
Michael E Jones
Catherine J Kennedy
Tomasz Kluz
Jennifer M Koziak
Jaime Lesnock
Jenny Lester
Jan Lubiński
Teri A Longacre
Maria Lycke
Constantina Mateoiu
Bryan M McCauley
Valerie McGuire
Britta Ney
Alexander Olawaiye
Sandra Orsulic
Ana Osorio
Luis Paz-Ares
Teresa Ramón Y Cajal
Joseph H Rothstein
Matthias Ruebner
Minouk J Schoemaker
Mitul Shah
Raghwa Sharma
Mark E Sherman
Yurii B Shvetsov
Naveena Singh
Helen Steed
Sarah J Storr
Aline Talhouk
Nadia Traficante
Chen Wang
Alice S Whittemore
Martin Widschwendter
Lynne R Wilkens
Stacey J Winham
Javier Benitez
Andrew Berchuck
David D Bowtell
Francisco J Candido Dos Reis
Ian Campbell
Linda S Cook
Anna DeFazio
Jennifer A Doherty
Peter A Fasching
Renée T Fortner
María J García
Marc T Goodman
Ellen L Goode
Jacek Gronwald
David G Huntsman
Beth Y Karlan
Linda E Kelemen
Stefan Kommoss
Nhu D Le
Stewart G Martin
Usha Menon
Francesmary Modugno
Paul Dp Pharoah
Joellen M Schildkraut
Weiva Sieh
Annette Staebler
Karin Sundfeldt
Anthony J Swerdlow
Susan J Ramus
James D Brenton

Publication Date

5-1-2023

Journal

The Journal of Pathology

Abstract

Our objective was to test whether p53 expression status is associated with survival for women diagnosed with the most common ovarian carcinoma histotypes (high-grade serous carcinoma [HGSC], endometrioid carcinoma [EC], and clear cell carcinoma [CCC]) using a large multi-institutional cohort from the Ovarian Tumor Tissue Analysis (OTTA) consortium. p53 expression was assessed on 6,678 cases represented on tissue microarrays from 25 participating OTTA study sites using a previously validated immunohistochemical (IHC) assay as a surrogate for the presence and functional effect of TP53 mutations. Three abnormal expression patterns (overexpression, complete absence, and cytoplasmic) and the normal (wild type) pattern were recorded. Survival analyses were performed by histotype. The frequency of abnormal p53 expression was 93.4% (4,630/4,957) in HGSC compared to 11.9% (116/973) in EC and 11.5% (86/748) in CCC. In HGSC, there were no differences in overall survival across the abnormal p53 expression patterns. However, in EC and CCC, abnormal p53 expression was associated with an increased risk of death for women diagnosed with EC in multivariate analysis compared to normal p53 as the reference (hazard ratio [HR] = 2.18, 95% confidence interval [CI] 1.36-3.47, p = 0.0011) and with CCC (HR = 1.57, 95% CI 1.11-2.22, p = 0.012). Abnormal p53 was also associated with shorter overall survival in The International Federation of Gynecology and Obstetrics stage I/II EC and CCC. Our study provides further evidence that functional groups of TP53 mutations assessed by abnormal surrogate p53 IHC patterns are not associated with survival in HGSC. In contrast, we validate that abnormal p53 IHC is a strong independent prognostic marker for EC and demonstrate for the first time an independent prognostic association of abnormal p53 IHC with overall survival in patients with CCC.

Keywords

Humans, Female, Tumor Suppressor Protein p53, Ovarian /Neoplasms, Carcinoma, Ovarian Epithelial, Carcinoma, Endometrioid, ovarian cancer, high‐grade serous carcinoma, endometrioid, clear cell, TP53, p53, prognosis

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Associated Data

PMID: 36948887

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