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Expression of Nectin-4 and PD-L1 in Upper Tract Urothelial Carcinoma.
Tomiyama, Eisuke; Fujita, Kazutoshi; Rodriguez Pena, Maria Del Carmen; Taheri, Diana; Banno, Eri; Kato, Taigo; Hatano, Koji; Kawashima, Atsunari; Ujike, Takeshi; Uemura, Motohide; Takao, Tetsuya; Yamaguchi, Seiji; Fushimi, Hiroaki; Yoshimura, Kazuhiro; Uemura, Hirotsugu; Netto, George J; Nonomura, Norio.
Afiliación
  • Tomiyama E; Department of Urology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
  • Fujita K; Department of Urology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
  • Rodriguez Pena MDC; Department of Urology, Kindai University Faculty of Medicine, 377-2, Ohno-Higashi, Sayama, Osaka 589-8511, Japan.
  • Taheri D; Department of Pathology, Johns Hopkins University, Baltimore, MD 21287, USA.
  • Banno E; Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35233-7331, USA.
  • Kato T; Department of Pathology, Johns Hopkins University, Baltimore, MD 21287, USA.
  • Hatano K; Department of Pathology, Kidney Diseases Research Center, Isfahan University of Medical Sciences, Isfahan 8174673461, Iran.
  • Kawashima A; Department of Urology, Kindai University Faculty of Medicine, 377-2, Ohno-Higashi, Sayama, Osaka 589-8511, Japan.
  • Ujike T; Department of Urology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
  • Uemura M; Department of Urological Immuno-Oncology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
  • Takao T; Department of Urology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
  • Yamaguchi S; Department of Urology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
  • Fushimi H; Department of Urology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
  • Yoshimura K; Department of Urology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
  • Uemura H; Department of Urological Immuno-Oncology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
  • Netto GJ; Department of Urology, Osaka General Medical Center, Osaka 558 8558, Japan.
  • Nonomura N; Department of Urology, Osaka General Medical Center, Osaka 558 8558, Japan.
Int J Mol Sci ; 21(15)2020 Jul 29.
Article en En | MEDLINE | ID: mdl-32751328
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma / Moléculas de Adhesión Celular / Regulación Neoplásica de la Expresión Génica / Neoplasias Urológicas / Antígeno B7-H1 Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Mol Sci Año: 2020 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma / Moléculas de Adhesión Celular / Regulación Neoplásica de la Expresión Génica / Neoplasias Urológicas / Antígeno B7-H1 Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Mol Sci Año: 2020 Tipo del documento: Article País de afiliación: Japón