Prognostic Value of P63 Expression in Muscle-Invasive Bladder Cancer and Association with Molecular Subtypes—Preliminary Report

Author:

Sanguedolce Francesca1,Falagario Ugo Giovanni2,Zanelli Magda3ORCID,Palicelli Andrea3ORCID,Zizzo Maurizio4ORCID,Ascani Stefano5,Tortorella Simona1,Busetto Gian Maria2ORCID,Cormio Angelo6ORCID,Carrieri Giuseppe2,Cormio Luigi27

Affiliation:

1. Pathology Unit, Policlinico Foggia, University of Foggia, 71122 Foggia, Italy

2. Department of Urology and Renal Transplantation, Policlinico Foggia, University of Foggia, 71122 Foggia, Italy

3. Pathology Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy

4. Surgical Oncology Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy

5. Pathology Unit, Azienda Ospedaliera Santa Maria di Terni, University of Perugia, 05100 Terni, Italy

6. Urology Unit, Azienda Ospedaliero-Universitaria Ospedali Riuniti Di Ancona, Università Politecnica Delle Marche, 60126 Ancona, Italy

7. Department of Urology, Bonomo Teaching Hospital, 76123 Andria, Italy

Abstract

There is an ongoing need for biomarkers that could reliably predict the outcome of BC and that could guide the management of this disease. In this setting, we aimed to explore the prognostic value of the transcription factor P63 in patients with muscle-invasive bladder cancer (MIBC) having undergone radical cystectomy. The correlation between P63 expression and clinicopathological features (tumor stage, nodes involvement, patterns of muscularis propria invasion, papillary architecture, anaplasia, concomitant carcinoma in situ, lymphovascular invasion, perineural invasion, necrosis) and molecular subtyping (basal and luminal type tumors) was tested in 65 radical cystectomy specimens and matched with cancer-specific survival (CSS) and overall survival (OS). P63-negative tumors displayed significantly higher rates of pattern 2 of muscularis propria invasion (50% vs. 14%, p = 0.002) and variant histology (45% vs. 19%, p = 0.022) compared to P63-positive ones. According to the combined expression of CK5/6 and CK20 (Algorithm #1), P63-positive and P63-negative tumors were mostly basal-like and double-negative, respectively (p = 0.004). Using Algorithm #2, based on the combined expression of CK5/6 and GATA3, the vast majority of tumors were luminal overall and in each group (p = 0.003). There was no significant difference in CSS and OS between P63-positive and P63-negative tumors, but the former featured a trend towards longer OS. Though associated with pathological features harboring negative prognostic potential, P63 status as such failed to predict CSS and OS. That said, it may contribute to better molecular subtyping of MIBC.

Publisher

MDPI AG

Reference43 articles.

1. (2023, January 31). Available online: https://gco.iarc.fr/today/.

2. Babjuk, M., Burger, M., Compérat, E., Gontero, P., Liedberg, F., Masson-Lecomte, A., Mostafid, A.H., Palou, J., Van Rhijn, B.W.G., and Roupret, M. (2022). EAU Guidelines on Non-Muscle-Invasive Bladder Cancer (TaT1 and CIS), EAU.

3. Witjes, J.A., Bruins, H.M., Carrión, A., Cathomas, R., Compérat, E.M., Efstathiou, J.A., Kietkau, R., Gakis, G., Van der Heijden, A.G., and Lorch, A. (2022). EAU Guidelines on Muscle-Invasive and Metastatic Bladder Cancer, EAU.

4. Non-muscle-invasive Bladder Cancer: Overview and Contemporary Treatment Landscape of Neoadjuvant Chemoablative Therapies;Matulewicz;Rev. Urol.,2020

5. Molecular markers in bladder cancer: Novel research frontiers;Sanguedolce;Crit. Rev. Clin. Lab. Sci.,2015

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