Predictive value of sphingosine kinase 1 expression in neoadjuvant treatment of breast cancer

被引:15
|
作者
Ruckhaeberle, Eugen [1 ]
Karn, Thomas [1 ]
Denkert, Carsten [2 ]
Loibl, Sibylle [3 ]
Ataseven, Beyhan [4 ]
Reimer, Toralf [5 ]
Becker, Sven [1 ]
Holtrich, Uwe [1 ]
Rody, Achim [6 ]
Darb-Esfahani, Silvia [2 ]
Nekljudova, Valentina [3 ]
von Minckwitz, Gunter [1 ,3 ]
机构
[1] Goethe Univ Frankfurt, Dept Obstet & Gynecol, D-60590 Frankfurt, Germany
[2] Charite, Dept Pathol, Berlin, Germany
[3] German Breast Grp GmbH, Neu Isenburg, Germany
[4] Rotkreuzklinikum, Dept Obstet & Gynecol, Munich, Germany
[5] Sudstadt Klinikum, Dept Obstet & Gynecol, Rostock, Germany
[6] Univ Schleswig Holstein, Dept Obstet & Gynecol, Lubeck, Germany
关键词
Breast cancer; Neoadjuvant systemic therapy; Sphingolipids; Prediction of response; 1-PHOSPHATE RECEPTORS; MOLECULAR SUBTYPES; CELL-DEATH; CHEMOTHERAPY; THERAPY; SPHINGOSINE-1-PHOSPHATE; CYCLOPHOSPHAMIDE; RECOMMENDATIONS; SPHINGOLIPIDS; SENSITIVITY;
D O I
10.1007/s00432-013-1490-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sphingolipids play important roles in apoptosis and cell proliferation. Sphingosine kinase 1 (SphK1) expression has a prognostic impact in primary breast cancer, but its predictive value is currently unknown. A total of 112 breast cancer specimens from a prospective neoadjuvant chemotherapy trial (GeparDuo) were studied. Using tissue microarrays of pre-treatment core cut biopsies, we determined the expression of SphK1 by immunohistochemistry. The upper quartile of the cohort according to an immune reactive score of SphK1 was used as cutoff for high expression. We observed a larger number of samples with high SphK1 expression among ER-negative cancers (36.8 vs. 20.5 % among ER-positive cancers; Fisher test p = 0.073). Eighteen of the 112 patients demonstrated a pathological complete response. A significant predictive value for pathological complete response was observed for ER negativity (p = 0.003), young age (p = 0.037), and high tumor grade (p = 0.049). An increased pCR rate was observed in tumors with high SphK1 expression within the luminal subtype (26.7 vs. 5.8 %; Fisher test p = 0.040). No significant difference in survival was detected according to SphK1 expression. Our results suggest that SphK1 may be a predictive factor for pCR after neoadjuvant treatment in luminal type breast cancers and warrants further investigation.
引用
收藏
页码:1681 / 1689
页数:9
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