Should a borderline negative HER2 result in a core biopsy of invasive carcinoma of the breast have HER2 assessment repeated in the excision specimen?

被引:0
作者
Lee, Andrew H. S. [1 ]
Hodi, Zsolt [1 ,2 ]
Abbas, Areeg [1 ]
Wencyk, Peter [2 ]
Ellis, Ian O. [1 ,2 ]
Rakha, Emad [1 ]
机构
[1] Nottingham Univ Hosp NHS Trust, Histopathol Dept, Nottingham, England
[2] Source Biosci Plc, Nottingham, England
关键词
carcinoma; breast; in situ hybridisation; CANCER AMERICAN SOCIETY; CLINICAL ONCOLOGY/COLLEGE; RECOMMENDATIONS; UK;
D O I
10.1136/jcp-2023-209091
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
AimThe 2015 UK guidelines for HER2 assessment in breast cancer recommended repeat assessment if the core biopsy was scored as 2+ on HER2 immunohistochemistry (IHC) with borderline negative in situ hybridisation (ratio of number of HER2 to chromosome 17 centromere copies of 1.8-1.99). This case series aimed to assess the value of such repeat assessment in the surgical specimen, in particular the proportion that were HER2 positive.MethodsDetails of biopsies with 2+ IHC and borderline negative in situ hybridisation were extracted from a database. The results of repeat HER2 testing in the surgical specimen for this cohort study were then obtained.Results112 patients with no preoperative treatment had repeat assessment: 4 were 3+ and 16 were 2+ amplified. Of 14 with preoperative chemotherapy, 1 was 3+ and 4 were 2+ amplified. All the 2+ amplified carcinomas had a HER2 to chromosome 17 ratio less than 4, in 50% the ratio was between 2.0 and 2.2, and in 50% the HER2 copy number was less than 4.ConclusionsRepeat assessment yielded 4% 3+ results and 14% 2+ amplified carcinomas but with low level amplification. These results suggest that retesting of borderline negative HER2 cases should be optional and no longer mandatory.
引用
收藏
页码:726 / 729
页数:4
相关论文
共 15 条
  • [11] HER2 testing in the UK: further update to recommendations
    Walker, R. A.
    Bartlett, J. M. S.
    Dowsett, M.
    Ellis, I. O.
    Hanby, A. M.
    Jasani, B.
    Miller, K.
    Pinder, S. E.
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 2008, 61 (07) : 818 - 824
  • [12] Wolff AC, 2007, ARCH PATHOL LAB MED, V131, P18, DOI 10.1043/1543-2165(2007)131[18:ASOCCO]2.0.CO
  • [13] 2
  • [14] Wolff AC, 2018, J CLIN ONCOL, V36, P2105, DOI [10.1200/JCO.2018.77.8738, 10.5858/arpa.2018-0902-SA]
  • [15] Wolff AC, 2013, J CLIN ONCOL, V31, P3997, DOI [10.1200/JCO.2013.50.9984, 10.5858/arpa.2013-0953-SA]