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PD-L2: A prognostic marker in chromophobe renal cell carcinoma?
Erlmeier, Franziska; Weichert, Wilko; Autenrieth, Michael; Wiedemann, Max; Schrader, Andres Jan; Hartmann, Arndt; Ivanyi, Philipp; Steffens, Sandra.
Afiliação
  • Erlmeier F; Institute of Pathology, Technical University Munich (TUM), Trogerstraße 18, 81675, Munich, Germany. f.erlmeier@tum.de.
  • Weichert W; Member of the German Renal Cell Tumor Consortium, Jena, Germany. f.erlmeier@tum.de.
  • Autenrieth M; Institute of Pathology, Technical University Munich (TUM), Trogerstraße 18, 81675, Munich, Germany.
  • Wiedemann M; Member of the German Cancer Consortium (DKTK), Heidelberg, Germany.
  • Schrader AJ; Department of Urology, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.
  • Hartmann A; The Munich Cancer Registry of the Tumorzentrum Munich, Institute of Medical Information Processing, Biometry and Epidemiology, Ludwig-Maximilians-University Munich, Munich, Germany.
  • Ivanyi P; Member of the German Renal Cell Tumor Consortium, Jena, Germany.
  • Steffens S; Clinic for Urology, University Hospital Muenster, Münster, Germany.
Med Oncol ; 34(5): 71, 2017 May.
Article em En | MEDLINE | ID: mdl-28353093
ABSTRACT
In the context of cancer immunotherapy, PD-1 as well as PD-L1 has been widely studied in renal cell carcinoma (RCC). PD-1 and PD-L1 play a significant role as prognostic markers in clear cell renal cell carcinoma. In contrast, little is known about PD-L2 expression patterns in RCC, especially in rarer subtypes. The aim of this study was to evaluate the prevalence, distribution and prognostic impact of PD-L2 expression in chromophobe (ch)RCC. Eighty-one patients who underwent renal surgery due to chRCC were retrospectively evaluated. Tumor specimens were analyzed for PD-L2 expression by immunohistochemistry. Expression data were associated with clinicopathological parameters and overall survival (OS). Twenty-three (28.4%) patients showed a PD-L2 > median (PD-L2 high) staining intensity. No significant association between clinicopathological parameters and PD-L2 expression was identified. A significant difference between 5- and 10-year OS in dependence of PD-L2 expression was found (PD-L2 low 96.4 and 87.7% vs. PD-L2 high 87.1 and 56%; log rank, p = 0.029). However, in multivariate analysis PD-L2 expression failed to be proofed as an independent prognostic factor. In conclusion, to our knowledge this is the first study evaluating the prognostic impact of PD-L2 in a considerably large cohort of chRCC. Our results showed a significant diminished OS in dependence of PD-L2 expression. This implicates that PD-L2 might play a role as prognostic marker in chRCC demanding further evaluation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Biomarcadores Tumorais / Proteína 2 Ligante de Morte Celular Programada 1 / Neoplasias Renais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Biomarcadores Tumorais / Proteína 2 Ligante de Morte Celular Programada 1 / Neoplasias Renais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article