Monitoring serum HER2 levels in breast cancer patients

被引:25
作者
Tchou, Julia [1 ]
Lam, Lian [2 ]
Li, Yun Rose [3 ,4 ,5 ]
Edwards, Claire [1 ]
Ky, Bonnie [6 ]
Zhang, Hongtao [2 ]
机构
[1] Univ Penn, Div Endocrine & Oncol Surg, Perelman Sch Med, Rena Rowan Breast Ctr,Abramson Canc Ctr, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Med Sci Training Program, Philadelphia, PA 19104 USA
[4] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[5] Childrens Hosp Philadelphia, Ctr Appl Genom, Philadelphia, PA 19104 USA
[6] Univ Penn, Div Cardiovasc Med, Perelman Sch Med, Philadelphia, PA 19104 USA
来源
SPRINGERPLUS | 2015年 / 4卷
关键词
HER2/neu; SHER2; Biomarker; MBB buffer; Breast cancer; EXTRACELLULAR DOMAIN; CLINICAL UTILITY; MONOCLONAL-ANTIBODY; CHEMOTHERAPY; THERAPIES; SURVIVAL; COMPLEX; PROTEIN; CELLS;
D O I
10.1186/s40064-015-1015-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: We have developed a new approach to reduce the serum interference for ELISA. The purpose of this study is to investigate if we can use the optimized ELISA (MBB-ELISA) to detect serum soluble HER2/neu (sHER2) in early stage primary breast cancer and monitor its change during treatments. Findings: We collected sera preoperatively from 118 primary breast cancer patients. Serum samples were also collected sequentially from a subset of patients during and after adjuvant treatment. sHER2 in these samples was measured by the MBB-ELISA. Only 16.7 % of tissue HER2 (tHER2) positive patients had significantly elevated sHER2 levels in serum. Interestingly, sera of some patients with tHER2 negative tumors, including those that were 2+ by IHC but negative by FISH, demonstrated slightly elevated sHER2 levels. Multivariate analysis demonstrated that patients with elevated sHER2 (> = 7 ng/ml) had significantly worse disease free survival. During treatments, sHER2 levels consistently fell in response to adjuvant therapies. Nevertheless, in all 4 patients who developed metastases, a steady rise in sHER2 levels was noted before metastatic disease became clinically evident. Conclusions: For early stage breast cancers, sHER2 is a poor biomarker to predict tHER2 status, but may have value to supplement tissue tests to identify patients with HER2 tumors. Our results also suggest that sHER2 is worth further study as a biomarker to monitor breast cancer patients during treatments.
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页数:7
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