Trophoblast cell surface antigen‐2: a promising new biomarker and potential therapeutic target in penile squamous cell carcinoma

Author:

Weiten Richard12ORCID,Storz Enno1ORCID,Kessler Carolina1,Sperber Laurenz1,Spohn Hanna Elisa1,Pfister David1ORCID,Nestler Tim3,Tolkach Yuri4,Linden Friederike5,Wirtz Ralph5,von Brandenstein Melanie1,Krausewitz Philipp2ORCID,Heidenreich Axel16ORCID

Affiliation:

1. Department of Urology Uro‐Oncology, Robot‐Assisted and Specialized Urologic Surgery University Hospital Cologne Cologne Germany

2. Department of Urology and Paediatric Urology University Hospital Bonn Bonn Germany

3. Department of Urology Federal Armed Services Hospital Koblenz Koblenz Germany

4. Institute of Pathology University Hospital Cologne Cologne Germany

5. STRATIFYER Molecular Pathology GmbH Cologne Germany

6. Department of Urology Medical University Vienna Vienna Austria

Abstract

ObjectiveTo evaluate the potential utility of antibody‐drug conjugates targeting trophoblast cell surface antigen‐2 (TROP‐2) in patients with primary penile squamous cell carcinoma (PSCC), patients with recurrence (REC cohort), and patient‐matched distant metastases (MET cohort), and to assess the potential use of TROP‐2 as a predictive non‐invasive biomarker in PSCC.MethodsA cohort comprising a PRIM (n = 37), REC (n = 5) and MET subcohort (n = 7), with MET including lymph node and lung metastases, was analysed using quantitative real‐time PCR, ELISA and immunohistochemical staining with evaluation of H‐score.ResultsTROP‐2 mRNA and serum protein levels were significantly increased in primary and recurrent PSCC compared to cancer‐free controls (both P < 0.001). Immunohistochemical analysis revealed that most of the PRIM cohort (n = 34/37, median H‐score 260, interquartile range [IQR] 210–300), as well as all patients in the REC (median [IQR] H‐score 200 [165–290]) and MET cohorts (median [IQR] H‐score 280 [260–300]) exhibited moderate to strong membranous TROP‐2 expression. Additionally, The H‐score (membranous TROP‐2 expression) was positively correlated with TROP‐2 mRNA (ρ = 0.69, P < 0.0001, R2 = 0.70) and protein levels (ρ = 0.86, P < 0.0001, R2 = 0.59), indicating its potential as a non‐invasive biomarker in PSCC.ConclusionIn summary, our results support further studies on TROP‐2 as a diagnostic and therapeutic target in primary, recurrent and metastatic PSCC.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

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