Expression of excision repair cross complementing group 1 and prognosis in adrenocortical carcinoma patients treated with platinum-based chemotherapy

被引:52
作者
Ronchi, Cristina L. [1 ,2 ]
Sbiera, Silviu [1 ]
Kraus, Luitgard [1 ]
Wortmann, Sebastian [1 ]
Johanssen, Sarah [1 ]
Adam, Patrick [3 ]
Willenberg, Holger S. [4 ]
Hahner, Stefanie [1 ]
Allolio, Bruno [1 ]
Fassnacht, Martin [1 ]
机构
[1] Univ Wurzburg, Univ Hosp, Dept Med 1, Endocrine & Diabet Unit, D-97080 Wurzburg, Germany
[2] Univ Milan, Fdn IRCCS Osped Maggiore Policlin, Endocrine Unit, Milan, Italy
[3] Univ Wurzburg, Inst Pathol, D-8700 Wurzburg, Germany
[4] Univ Hosp Dusseldorf, Dept Endocrinol Diabet & Rheumatol, Dusseldorf, Germany
关键词
CELL LUNG-CANCER; THYMIDYLATE SYNTHASE; GENE-EXPRESSION; OVARIAN-CANCER; DNA-REPAIR; ERCC1; CISPLATIN; SURVIVAL; TUMORS; MANAGEMENT;
D O I
10.1677/ERC-08-0224
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Therapeutic progress in adrenocortical carcinoma (ACC) is severely hampered by its low incidence. Platinum-based chemotherapies are the most effective cytotoxic treatment regimens in ACC but response rates remain <50%. In other tumor entities, expression of excision repair cross complementing group 1 (ERCC1) predicts resistance to platinum compounds Therefore, we correlated ERCC1 protein expression and clinical outcome. We have retrolectively established adrenal tissue microarrays and analyzed prospectively samples from 163 ACCs, 15 benign adrenal adenomas, and 8 normal adrenal glands by immunohistochemistry for ERCC1 protein expression Detailed clinical data were available by the German ACC Registry ERCC1 protein was highly expressed in all normal adrenal glands, 14 benign tumors (93%) and in 75 ACCs (47%) In ACC, no differences in baseline parameters were found between patients with and without ERCC1 expression. Detection of ERCC1 was not correlated with survival in patients who never received platinum-based chemotherapy. In platinum-treated patients (n=45), objective response to platinum compounds was observed in 3/21 patients (14.3%) with high ERCC1 expression and in 7/24 patients (29.2%) with low ERCC1 expression (P=0.23). ERCC1 expression was strongly correlated with overall survival after platinum treatment (median: eight months in patients with high ERCC1 versus 24 months in low ERCC1 expression, hazard ratio (HR) 2.95 (95% confidence interval (CI) 1.4-6.2), P=0.004). Multivariate analysis confirmed that high ERCC1 expression was a predictive factor for poor prognosis in platinum treated patients (HR 2 2, 95% Cl 1.0-4.5, P=0.038) Our findings suggest that ERCC1 expression is the first factor for predicting survival in ACC patients treated with platinum-based chemotherapy
引用
收藏
页码:907 / 918
页数:12
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