KRT20, KRT5, ESR1 and ERBB2 expression can predict pathologic outcome in patients undergoing neoadjuvant chemotherapy and radical cystectomy for muscle-invasive bladder cancer

• Verfasst von: Jütte, Hendrik Jan [VerfasserIn]
• Verfasst von: Reike, Moritz [VerfasserIn]
• Verfasst von: Wirtz, Ralph M. [VerfasserIn]
• Verfasst von: Kriegmair, Maximilian [VerfasserIn]
• Verfasst von: Erben, Philipp [VerfasserIn]
• Verfasst von: Tully, Karl [VerfasserIn]
• Verfasst von: Weyerer, Veronika [VerfasserIn]
• Verfasst von: Eckstein, Markus [VerfasserIn]
• Verfasst von: Hartmann, Arndt [VerfasserIn]
• Verfasst von: Eidt, Sebastian [VerfasserIn]
• Verfasst von: Wezel, Felix [VerfasserIn]
• Verfasst von: Bolenz, Christian [VerfasserIn]
• Verfasst von: Tannapfel, Andrea [VerfasserIn]
• Verfasst von: Noldus, Joachim [VerfasserIn]
• Verfasst von: Roghmann, Florian [VerfasserIn]
• Titel: KRT20, KRT5, ESR1 and ERBB2 expression can predict pathologic outcome in patients undergoing neoadjuvant chemotherapy and radical cystectomy for muscle-invasive bladder cancer
• Verf.angabe: Hendrik Jütte, Moritz Reike, Ralph M. Wirtz, Maximilian Kriegmair, Philipp Erben, Karl Tully, Veronika Weyerer, Markus Eckstein, Arndt Hartmann, Sebastian Eidt, Felix Wezel, Christian Bolenz, Andrea Tannapfel, Joachim Noldus and Florian Roghmann
• E-Jahr: 2021
• Jahr: 26 May 2021
• Umfang: 13 S.
• Fussnoten: Gesehen am 05.10.2021
• Titel Quelle: Enthalten in: Journal of Personalized Medicine
• Ort Quelle: Basel : MDPI, 2011
• Jahr Quelle: 2021
• Band/Heft Quelle: 11(2021), 6, Artikel-ID 473, Seite 1-13
• ISSN Quelle: 2075-4426
• DOI: doi:10.3390/jpm11060473
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: bladder cancer
• Sach-SW: chemotherapy
• Sach-SW: muscle invasive
• Sach-SW: risk stratification
• Sach-SW: subtype
• K10plus-PPN: 1772422061

Abstract

Patients with muscle-invasive bladder cancer (MIBC) that underwent neoadjuvant chemotherapy (NAC) prior to radical cystectomy (RC) show improved overall survival, especially those with pathological complete response (pCR). The response to NAC according to molecular subtypes has been discussed. Molecular targets such as estrogen receptor (ESR1) and human epidermal growth factor receptor 2 (ERBB2) play an important role in breast cancer management and have also been associated with urothelial bladder cancer. Hence, the association of Keratin 20 (KRT20) Keratin 5 (KRT5), ESR1, and ERBB2 mRNA expression in MIBC at transurethral resection (TUR-BT) with pCR after NAC was analyzed retrospectively. Formalin-fixed paraffin-embedded tumour tissue samples from TUR-BT of 54 patients (42 males, 12 females, median age of 64) with MIBC were analyzed for KRT20, KRT5, ESR1, and ERBB2 mRNA expression. After NAC, RC was performed, and the specimens were evaluated for pCR. Statistical analyses comprised nonparametric and chi2 testing, partition models, and Spearman correlation analyses. After NAC, 22 out of 54 patients (40.7%) had pCR. Tumours with an elevated expression of markers associated with luminal differentiation (KRT20, ERBB2, ESR1) were associated with a higher chance of pCR (55% vs. 15.8%, p = 0.009). Elevated ERBB2 expression was positively correlated with luminal expression features such as KRT20, and negatively with basal characteristics such as KRT5. Patients with MIBC showing a high expression of ERBB2, ESR1, or KRT20 have a significantly higher chance of pCR following NAC. These findings might improve patient selection for NAC in MIBC.