Plage Henning, Furlano Kira, Neymeyer Jörg, Weinberger Sarah, Gerdes Benedikt, Hubatsch Mandy, Ralla Bernhard, Franz Antonia, Fendler Annika, de Martino Michela, Roßner Florian, Schallenberg Simon, Elezkurtaj Sefer, Kluth Martina, Lennartz Maximilian, Blessin Niclas C, Marx Andreas H, Samtleben Henrik, Fisch Margit, Rink Michael, Kaczmarek Krystian, Ecke Thorsten, Hallmann Steffen, Koch Stefan, Adamini Nico, Minner Sarah, Simon Ronald, Sauter Guido, Weischenfeldt Joachim, Klatte Tobias, Schlomm Thorsten, Horst David, Zecha Henrik, Slojewski Marcin
Department of Urology Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health Berlin Germany.
Institute of Pathology Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health Berlin Germany.
BJUI Compass. 2024 Apr 2;5(6):585-592. doi: 10.1002/bco2.354. eCollection 2024 Jun.
Carcinoembryonic 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.
To 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.
CEA 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 ( < 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 ( > 0.25).
CEA 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.
癌胚抗原(CEA)是一种细胞表面糖蛋白,是一个很有前景的治疗靶点。血清中脱落CEA的检测可用于癌症患者的监测。
为评估CEA表达在尿路上皮膀胱癌中的潜在临床意义,采用组织芯片形式,通过免疫组织化学对2500多例尿路上皮膀胱癌中的CEA进行分析。
正常尿路上皮细胞中基本无CEA染色,但在30.4%的尿路上皮膀胱癌中可观察到CEA染色,其中弱阳性406例(16.7%)、中度阳性140例(5.8%)、强阳性192例(7.9%)。411例pTaG2低级别肿瘤中CEA阳性率为10.9%,178例pTaG2高级别肿瘤中为32.0%,93例pTaG3肿瘤中为43.0%(<0.0001)。在1335例pT2-4期癌中,CEA阳性率(34.1%)低于pTaG3肿瘤。在pT2-4期癌中,CEA染色与pT、pN、分级、L状态、V状态、总生存期、无复发生存期及癌症特异性生存期均无关(>0.25)。
在pTa肿瘤中,CEA随分级进展显著增加,且在相当一部分pT2-4期尿路上皮膀胱癌中表达。pT2-4期癌中CEA高阳性率为采用血清CEA检测监测这些癌症的临床进程提供了机会。此外,CEA阳性的尿路上皮癌是靶向抗CEA药物治疗的候选对象。