CEA (CEACAM5) expression is common in muscle‐invasive urothelial carcinoma of the bladder but unrelated to the disease course

Author:

Plage Henning1,Furlano Kira1,Neymeyer Jörg1,Weinberger Sarah1,Gerdes Benedikt1,Hubatsch Mandy1,Ralla Bernhard1,Franz Antonia1,Fendler Annika1,de Martino Michela1,Roßner Florian2,Schallenberg Simon2,Elezkurtaj Sefer2,Kluth Martina3,Lennartz Maximilian3,Blessin Niclas C.3,Marx Andreas H.4,Samtleben Henrik4,Fisch Margit5,Rink Michael6,Kaczmarek Krystian7,Ecke Thorsten8,Hallmann Steffen8,Koch Stefan9,Adamini Nico10,Minner Sarah3,Simon Ronald3ORCID,Sauter Guido3,Weischenfeldt Joachim11112,Klatte Tobias8,Schlomm Thorsten1,Horst David2,Zecha Henrik110,Slojewski Marcin7

Affiliation:

1. Department of Urology Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt‐Universität zu Berlin and Berlin Institute of Health Berlin Germany

2. Institute of Pathology Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt‐Universität zu Berlin and Berlin Institute of Health Berlin Germany

3. Institute of Pathology University Medical Center Hamburg‐Eppendorf Hamburg Germany

4. Department of Pathology Academic Hospital Fuerth Fuerth Germany

5. Department of Urology University Medical Center Hamburg‐Eppendorf Hamburg Germany

6. Department of Urology Marienhospital Hamburg Hamburg Germany

7. Department of Urology and Urological Oncology Pomeranian Medical University Szczecin Poland

8. Department of Urology Helios Hospital Bad Saarow Bad Saarow Germany

9. Department of Pathology Helios Hospital Bad Saarow Bad Saarow Germany

10. Department of Urology Albertinen Hospital Hamburg Germany

11. Biotech Research & Innovation Center (BRIC) University of Copenhagen Copenhagen Denmark

12. Finsen Laboratory Rigshospitalet Copenhagen Denmark

Abstract

AbstractObjectivesCarcinoembryonic antigen (CEA) is a cell surface glycoprotein that represents a promising therapeutic target. Serum measurement of shedded CEA can be utilized for monitoring of cancer patients.Material and MethodsTo evaluate the potential clinical significance of CEA expression in urothelial bladder neoplasms, CEA was analysed by immunohistochemistry in more than 2500 urothelial bladder carcinomas in a tissue microarray format.ResultsCEA staining was largely absent in normal urothelial cells but was observed in 30.4% of urothelial bladder carcinomas including 406 (16.7%) with weak, 140 (5.8%) with moderate, and 192 (7.9%) with strong staining. CEA positivity occurred in 10.9% of 411 pTaG2 low‐grade, 32.0% of 178 pTaG2 high‐grade, and 43.0% of 93 pTaG3 tumours (p < 0.0001). In 1335 pT2–4 carcinomas, CEA positivity (34.1%) was lower than in pTaG3 tumours. Within pT2–4 carcinomas, CEA staining was unrelated to pT, pN, grade, L‐status, V‐status, overall survival, recurrence free survival, and cancer specific survival (p > 0.25).ConclusionCEA increases markedly with grade progression in pTa tumours, and expression occurs in a significant fraction of pT2–4 urothelial bladder carcinomas. The high rate of CEA positivity in pT2–4 carcinomas offers the opportunity of using CEA serum measurement for monitoring the clinical course of these cancers. Moreover, CEA positive urothelial carcinomas are candidates for a treatment by targeted anti‐CEA drugs.

Publisher

Wiley

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