Epithelial cell adhesion molecule is an independent prognostic marker in clear cell renal carcinoma

被引:24
作者
Eichelberg, Christian [1 ]
Chun, Felix K. [1 ]
Bedke, Jens [2 ]
Heuer, Roman [1 ]
Adam, Meike [1 ]
Moch, Holger [3 ]
Terracciano, Luigi [4 ]
Hinrichs, Kristin [1 ]
Dahlem, Roland [1 ]
Fisch, Margit [1 ]
Schlomm, Thorsten [5 ]
Sauter, Guido [6 ]
Minner, Sarah [6 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Dept Urol, D-20246 Hamburg, Germany
[2] Univ Tubingen, Dept Urol, Tubingen, Germany
[3] Univ Zurich Hosp, Inst Surg Pathol, CH-8091 Zurich, Switzerland
[4] Univ Basel Hosp, Dept Mol Pathol, CH-4031 Basel, Switzerland
[5] Univ Med Ctr Hamburg Eppendorf, Dept Urol, Sect Prostate Canc Res, D-20246 Hamburg, Germany
[6] Univ Med Ctr Hamburg Eppendorf, Inst Pathol, D-20246 Hamburg, Germany
关键词
renal cell carcinoma; epithelial cell adhesion molecule (EPCAM); CD; 326; Prognosis; molecular marker; EP-CAM; CANCER-PATIENTS; TUMOR-MARKERS; EPCAM; EXPRESSION; SURVIVAL; ANTIGEN; PREDICT; CD326;
D O I
10.1002/ijc.27970
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Epithelial cell adhesion molecule (EPCAM) has recently attained a renewed interest as a candidate protein in diagnosis, prognostication and therapy of various tumor entities. The molecular epidemiology and prognostic relevance of EPCAM in renal cell carcinoma (RCC) and amongst the histological subtypes of RCC are unclear. We analyzed the prevalence and prognostic significance of EPCAM in a tumor tissue microarray composed of 1,088 independent RCCs samples by immunohistochemistry (IHC). We found significant variations of EPCAM IHC staining intensities in between the RCC subtypes: in papillary and chromophobe RCC, the majority of tumors (8993%) showed an at least weak EPCAM protein expression. In the largest subgroup, the clear cell (cc)RCC (n = 767), a negative EPCAM IHC was found in 1/3 of the patients and was associated with high-grade disease and nodal metastases. KaplanMeier analyses demonstrated a significant association between positive EPCAM IHC and prolonged overall survival, even in a subset of low-risk ccRCC. In multivariable analyses, EPCAM represented an independent risk factor of survival throughout all subgroups. For localized, low-grade ccRCC, information of EPCAM IHC raised predictive accuracy of a multivariate model by approximate to 5%, compared to T-stage and grade alone. Our findings indicate that EPCAM is an independent prognostic molecular marker in ccRCC and, especially in localized ccRCC, might be able to provide auxiliary information for a better prognostication.
引用
收藏
页码:2948 / 2955
页数:8
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