ERBB2 (HER2) protein expression in uterine sarcomas

被引:0
作者
Zafrakas, M. [1 ]
Zepiridis, L. [1 ]
Theodoridis, T. D. [1 ]
Venizelos, I. D. [2 ]
Papanicolaou, A. [1 ]
Agorastos, T. [1 ]
Bontis, J. N. [1 ]
机构
[1] Aristotle Univ Thessaloniki, Dept Obstet & Gynecol 1, Papageorgiou Gen Hosp, Thessaloniki 56403, Greece
[2] Hippokrateio Gen Hosp, Dept Pathol, Thessaloniki, Greece
关键词
Uterine sarcoma; ERBB2; HER2; Targeted therapy; Trastuzumab; Herceptin (R); Lapatinib; Tykerb (R); METASTATIC BREAST-CANCER; RECEPTOR TYROSINE KINASES; GROWTH-FACTOR RECEPTOR; OF-THE-LITERATURE; ADJUVANT CHEMOTHERAPY; GENE AMPLIFICATION; TRASTUZUMAB; CARCINOSARCOMA; HER-2/NEU; THERAPY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Multiple clinical trials in recent years have shown that breast cancer patients with primary tumors overexpressing ERBB2 can be effectively treated with specific forms of modern anti-ERBB2-targeted therapy. The aim of the present study was to analyze the expression of the ERBB2 (HER2) protein in uterine sarcomas, in order to investigate the possibility of applying this treatment modality in uterine sarcomas. Methods: The expression of ERBB2 has been analyzed immunohistochemical in formalin-fixed paraffin-embedded primary uterine sarcomas (n = 11). Results: Using a semi-quantitative immunohistochemical score, we found that ERBB2 expression was very weak in the majority of tumors, with only three sarcomas showing moderate ERBB2 expression. Published studies evaluating the same issue in small numbers of uterine sarcomas reached similar findings. Conclusion: Overall, ERBB2 expression appears to be weak in uterine sarcomas. However, targeted treatment might still be feasible in a subgroup of patients with uterine sarcomas overexpressing ERBB2.
引用
收藏
页码:292 / 294
页数:3
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