PD-L2: A prognostic marker in chromophobe renal cell carcinoma?

被引:18
|
作者
Erlmeier, Franziska [1 ,2 ]
Weichert, Wilko [1 ,3 ]
Autenrieth, Michael [4 ]
Wiedemann, Max [5 ]
Schrader, Andres Jan [2 ,6 ]
Hartmann, Arndt [2 ,7 ]
Ivanyi, Philipp [8 ]
Steffens, Sandra [2 ]
机构
[1] Tech Univ Munich, Inst Pathol, Trogerstr 18, D-81675 Munich, Germany
[2] German Renal Cell Tumor Consortium, Jena, Germany
[3] German Canc Consortium DKTK, Heidelberg, Germany
[4] Tech Univ Munich, Dept Urol, Klinikum Rechts Isar, Munich, Germany
[5] Ludwig Maximilians Univ Munchen, Inst Med Informat Proc Biometry & Epidemiol, Munich Canc Registry Tumorzentrum Munich, Munich, Germany
[6] Univ Hosp Muenster, Clin Urol, Munster, Germany
[7] Univ Hosp Erlangen, Inst Pathol, Erlangen, Germany
[8] Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpl, Hannover, Germany
关键词
Renal cell carcinoma; PD-L2; Chromophobe histology; Survival; 1 PROTEIN EXPRESSION; ANTI-PD-L1; ANTIBODY; CANCER; LIGAND; DEATH; ACTIVATION; SAFETY; MEMBER;
D O I
10.1007/s12032-017-0926-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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). Twentythree (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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页数:6
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