Phosphorylated HER3 and FITC-labeled trastuzumab immunohistochemistry in patients with HER2-positive breast cancer treated with adjuvant trastuzumab

被引:2
作者
Kanomata, Naoki [1 ]
Kurebayashi, Junichi [2 ]
Moriya, Takuya [1 ]
机构
[1] Kawasaki Med Sch, Dept Pathol, Matsushima 577, Kurashiki, Okayama 7010192, Japan
[2] Kawasaki Med Sch, Dept Breast & Thyroid Surg, Kurashiki, Okayama, Japan
关键词
Phosphorylated HER3; HER3; HER2; Trastuzumab; Breast cancer; EPIDERMAL-GROWTH-FACTOR; PHOSPHATIDYLINOSITOL; 3-KINASE; SIGNAL-TRANSDUCTION; RESISTANCE; RECEPTOR; ERBB3; ACTIVATION; SURVIVAL; BINDING; PERTUZUMAB;
D O I
10.1007/s00795-018-0208-9
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The development of trastuzumab has significantly improved the prognosis of HER2-positive breast cancer. However, disease recurs in some patients with HER2-positive breast cancer. A new strategy for treating HER2-positive breast cancer is necessary. Although several studies have reported that HER3 is a prognostic factor for HER2-positive breast cancers, phosphorylated HER3 (pHER3) has not been well studied. There has been no survival analysis including immunohistochemistry with trastuzumab as the primary antibody. We analyzed immunohistochemistry using anti-pHER3 antibody and FITC-labeled trastuzumab (FITC-tra). Of 78 patients enrolled in the study, we could evaluate the immunohistochemistry for pHER3 in 71 cases and that for FITC-tra in 72 cases. Sixteen cases were positive for pHER3 (16/71, 22.5%), and 19 positive for FITC-tra (19/72, 26.4%). Kaplan-Meier analysis showed a significant association of pHER3 positivity (p = 0.011) but not HER3 positivity or FITC-tra positivity with disease-free survival. Therefore, immunohistochemical evaluation of pHER3 in HER2-positive breast cancer may provide a useful biomarker. An expanded study of pHER3 involving standardization of the pHER3 test to be encouraged.
引用
收藏
页码:106 / 113
页数:8
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