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Published in: Diagnostic Pathology 1/2015

Open Access 01-12-2015 | Research

PD-L1 expression in renal cell carcinoma clear cell type is related to unfavorable prognosis

Authors: Katia R M Leite, Sabrina T. Reis, José Pontes Junior, Marcelo Zerati, Daniel de Oliveira Gomes, Luiz H. Camara-Lopes, Miguel Srougi

Published in: Diagnostic Pathology | Issue 1/2015

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Abstract

Background

PD-L1 is a glycoprotein from the family of T-cell co-stimulatory molecules that are constitutively expressed by macrophages. Aberrant expression of PD-L1 is observed in human cancers associated with inhibition of the tumor-directed T-cell immune response. There are few reports in the literature evaluating PD-L1 expression in association to prognosis specifically in renal cell cancer clear cell type (RCC-CC).

Methods

Immunohistochemistry using a PD-L1 polyclonal antibody was performed on a tissue microarray (TMA) that contained 115 surgical specimens of RCC-CC. Cases were classified based on the absence or presence of staining intensity in the cytoplasm and membranes of the tumor cells. Statistical analysis was used to determine the association of PD-L1 expression with classic prognostic factors and tumor recurrence.

Results

PD-L1 expression was positive in 56.5 % of tumors. The univariate analysis showed a correlation between PD-L1 expression and nuclear Fuhrman grade (p = 0.021) and microvascular tumor embolization (p = 0.039). One hundred and four patients were monitored for a mean time of 115.7 months. Seventeen patients (16.3 %) suffered tumor recurrence. Negative outcomes were associated with higher nuclear grade tumors, PD-L1 expression, and the presence of microvascular invasion.

Conclusion

Our findings confirm that PD-L1 expression is an important prognostic factor in RCC-CC.
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Metadata
Title
PD-L1 expression in renal cell carcinoma clear cell type is related to unfavorable prognosis
Authors
Katia R M Leite
Sabrina T. Reis
José Pontes Junior
Marcelo Zerati
Daniel de Oliveira Gomes
Luiz H. Camara-Lopes
Miguel Srougi
Publication date
01-12-2015
Publisher
BioMed Central
Published in
Diagnostic Pathology / Issue 1/2015
Electronic ISSN: 1746-1596
DOI
https://doi.org/10.1186/s13000-015-0414-x

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