TP53 mutation and abnormal p53 expression in endometrial cancer: Associations with race and outcomes

This multi-center cohort study assessed associations between race, TP53 mutations, p53 expression, and histology to investigate racial survival disparities in endometrial cancer (EC). Black and White patients with advanced or recurrent EC with Next Generation Sequencing data in the Endometrial Cance...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Gynecologic oncology 2023-11, Vol.178, p.44-53
Hauptverfasser: Whelan, Karley, Dillon, Mairead, Strickland, Kyle C., Pothuri, Bhavana, Bae-Jump, Victoria, Borden, Lindsay E., Thaker, Premal H., Haight, Paulina, Arend, Rebecca C., Ko, Emily, Jackson, Amanda L., Corr, Bradley R., Ayoola-Adeola, Martins, Wright, Jason D., Podwika, Sarah, Smitherman, Carson, Thomas, Samantha, Lightfoot, Michelle, Newton, Meredith, Washington, Christina, Mullen, Mary, Cosgrove, Casey, Harsono, Alfonsus Adrian Hadikusumo, Powell, Kristina, Herzog, Thomas J., Salani, Ritu, Alvarez Secord, Angeles
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:This multi-center cohort study assessed associations between race, TP53 mutations, p53 expression, and histology to investigate racial survival disparities in endometrial cancer (EC). Black and White patients with advanced or recurrent EC with Next Generation Sequencing data in the Endometrial Cancer Molecularly Targeted Therapy Consortium database were identified. Clinicopathologic and treatment variables were summarized by race and compared. Overall survival (OS) and progression-free survival (PFS) among all patients were estimated by the Kaplan-Meier method. Cox proportional hazards models estimated the association between race, TP53 status, p53 expression, histology, and survival outcomes. Black patients were more likely than White patients to have TP53-mutated (N = 727, 71.7% vs 49.7%, p 
ISSN:0090-8258
1095-6859
1095-6859
DOI:10.1016/j.ygyno.2023.09.009