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Expression of Nectin-4 and Pd-L1 in Upper Tract Urothelial Carcinoma Publisher Pubmed



Tomiyama E1 ; Fujita K1, 2 ; Rodriguez Pena MDC3, 4 ; Taheri D3, 5 ; Banno E2 ; Kato T1, 6 ; Hatano K1 ; Kawashima A1 ; Ujike T1 ; Uemura M1, 6 ; Takao T7 ; Yamaguchi S7 ; Fushimi H8 ; Yoshimura K2 Show All Authors
Authors
  1. Tomiyama E1
  2. Fujita K1, 2
  3. Rodriguez Pena MDC3, 4
  4. Taheri D3, 5
  5. Banno E2
  6. Kato T1, 6
  7. Hatano K1
  8. Kawashima A1
  9. Ujike T1
  10. Uemura M1, 6
  11. Takao T7
  12. Yamaguchi S7
  13. Fushimi H8
  14. Yoshimura K2
  15. Uemura H2
  16. Netto GJ3, 4
  17. Nonomura N1
Show Affiliations
Authors Affiliations
  1. 1. Department of Urology, Osaka University Graduate School of Medicine, Osaka, 565-0871, Japan
  2. 2. Department of Urology, Kindai University, Faculty of Medicine, 377-2, Ohno-Higashi Osaka, Sayama, 589-8511, Japan
  3. 3. Department of Pathology, Johns Hopkins University, Baltimore, 21287, MD, United States
  4. 4. Department of Pathology, University of Alabama at Birmingham, Birmingham, 35233-7331, AL, United States
  5. 5. Department of Pathology, Kidney Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, 8174673461, Iran
  6. 6. Department of Urological Immuno-Oncology, Osaka University Graduate School of Medicine, Osaka, 565-0871, Japan
  7. 7. Department of Urology, Osaka General Medical Center, Osaka, 558 8558, Japan
  8. 8. Department of Pathology, Osaka General Medical Center, Osaka, 558 8558, Japan

Source: International Journal of Molecular Sciences Published:2020


Abstract

Enfortumab vedotin is a novel antibody–drug conjugate targeting Nectin-4, which is highly expressed in urothelial carcinoma. However, the expression status of Nectin-4 in upper tract urothelial carcinoma (UTUC) remains unclear. The relationship between Nectin-4 and Programmed Death Ligand 1 (PD-L1) in UTUC is also ambiguous. We performed immunohistochemical analysis of 99 UTUC tissue microarray to assess the expression of Nectin-4 and PD-L1 in UTUC. Nectin-4-positivity was detected in 65 (65.7%) samples, and PD-L1 was detected in 24 (24.2%) samples. There was no correlation between the expression of Nectin-4 and PD-L1. Patients with strong Nectin-4-expressing tumors had a significantly higher risk of progression (p = 0.031) and cancer-specific mortality (p = 0.036). Strong Nectin-4 expression was also an independent predictor of disease progression in the high-risk group (pT3 ≤ or presence of lymphovascular invasion or lymph node metastasis) (Hazard ratio, 3.32 [95% confidence interval, 1.20–7.98; p = 0.027]). In conclusion, we demonstrated that Nectin-4 expression rate in UTUC was 65.7% and independent of PD-L1 expression. Strong Nectin-4 expression was associated with worse progression-free survival in high-risk UTUC. These findings suggested that enfortumab vedotin may be effective in a broad range of patients with UTUC, regardless of PD-L1 expression. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.