Assessment of HER2 status in invasive breast cancers with increased centromere 17 copy number

被引:23
|
作者
Jang, Min Hye [1 ,2 ]
Kim, Eun Joo [1 ]
Kim, Hyun Jeong [1 ]
Chung, Yul Ri [2 ]
Park, So Yeon [1 ,2 ]
机构
[1] Seoul Natl Univ, Bundang Hosp, Dept Pathol, Songnam 463707, Gyeonggi, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 151, South Korea
关键词
Breast cancer; HER2; Fluorescence in situ hybridization; Polysomy; 17; Reference gene; IN-SITU HYBRIDIZATION; CHROMOSOME-17; POLYSOMY; AMERICAN-SOCIETY; HER-2/NEU STATUS; GENE STATUS; AMPLIFICATION; TRUE; RECOMMENDATIONS; CARCINOMAS; EXPRESSION;
D O I
10.1007/s10549-015-3522-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study was designed to evaluate usefulness of additional fluorescence in situ hybridization (FISH) using other reference genes on chromosome 17 for assessment of HER2 status in invasive breast cancers with increased centromere 17 copy number, and to compare this approach with conventional methods based on the 2007 and 2013 ASCO/CAP guidelines. We performed FISH with probes for SMS, RARA, and TP53 on 253 breast cancers with centromeric probe CEP17 copy number a parts per thousand yen2.6 using tissue microarrays. If one or more gene had a mean copy number < 2.6, the largest number for that gene(s) was chosen as an alternative to CEP17 copy number. Of the 243 cases in which re-grading was possible, only 2 had copy numbers a parts per thousand yen2.6 for RARA, SMS, and TP53. Of the 151 breast cancers which were considered HER2 non-amplified by the 2007 ASCO/CAP guidelines using the HER2:CEP17 ratio, 42 (27.8 %) were re-graded as amplified and 33 (21.8 %) as equivocal after FISH using additional reference genes. Of the 101 HER2-non-amplified cases by the 2013 ASCO/CAP guidelines, 2 (2.0 %) were reclassified as amplified and 24 (23.8 %) as equivocal. Of 46 equivocal cases, 35 (76.1 %) were re-graded as amplified. After re-grading, HER2-amplified cases were significantly increased, and the concordance between HER2 FISH and HER2 immunohistochemistry decreased. And some pathologic features of the cases which were designated to have HER2 amplification after additional FISH were not compatible with those of HER2-amplified breast cancers. The use of additional reference genes has been suggested as an option for accurate assessment of HER2 status in breast cancers with increased CEP17 copy number. However, this has limitations in that it can cause over-grading of HER2 status in tumors that lose the new reference genes. Thus, at present, it seems that additional FISH using other reference gene such as SMS, RARA, and TP53 for the cases with increased CEP17 copy number is not suitable for daily practice.
引用
收藏
页码:67 / 77
页数:11
相关论文
共 50 条
  • [31] A clinicopathological study and survival analysis of 99 breast cancers with HER2/CEP17 ratio ≥ 2.0 and an average HER2 copy number < 4.0 per cell in China
    Shuling Zhou
    Hong Lv
    Anqi Li
    Ming Li
    Siyuan Zhong
    Hongfen Lu
    Xiaoyan Zhou
    Qianming Bai
    Wentao Yang
    BMC Cancer, 23
  • [32] Assessment of HER2 status in breast cancer
    Penault-Llorca, F
    Cayre, A
    BULLETIN DU CANCER, 2004, 91 : S211 - S215
  • [33] Neoadjuvant Treatment in Breast Cancer; Relationship to HER2 status including HER2 Copy Number using Brightfield Dual in situ Hybridization
    Neville, Grace
    O'Connell, Fionnuala
    Bennett, Michael
    Feeley, Linda
    O'Reilly, Seamus
    Browne, Tara Jane
    LABORATORY INVESTIGATION, 2018, 98 : 95 - 95
  • [34] Neoadjuvant Treatment in Breast Cancer; Relationship to HER2 status including HER2 Copy Number using Brightfield Dual in situ Hybridization
    Neville, Grace
    O'Connell, Fionnuala
    Bennett, Michael
    Feeley, Linda
    O'Reilly, Seamus
    Browne, Tara Jane
    MODERN PATHOLOGY, 2018, 31 : 95 - 95
  • [35] Her2/neu status in bone metastases of breast cancers
    Lörincz, T
    Tóth, J
    Szendröi, M
    Tímár, J
    PROCEEDINGS OF THE 2ND CONGRESS OF THE WORLD SOCIETY FOR BREAST HEALTH, 2003, : 35 - 38
  • [36] A clinicopathological study and survival analysis of 99 breast cancers with HER2/CEP17 ratio ≥ 2.0 and an average HER2 copy number &lt; 4.0 per cell in China
    Zhou, Shuling
    Lv, Hong
    Li, Anqi
    Li, Ming
    Zhong, Siyuan
    Lu, Hongfen
    Zhou, Xiaoyan
    Bai, Qianming
    Yang, Wentao
    BMC CANCER, 2023, 23 (01)
  • [37] HER2 in-Situ hybridization positive breast cancers with HER2/CEP17 ratio ≥2.0 and average HER2 copy number <4.0 are frequently discordant with HER2 immunohistochemistry results: Implications for potential modification of testing algorithm
    Livasy, Chad
    Johnson, Nicole
    Domfeh, Akosua
    CANCER RESEARCH, 2018, 78 (04)
  • [38] Integrated Analysis of HER2 Copy Number by Cytogenomic Microarray in Breast Cancers With Nonclassical In Situ Hybridization Results
    Haskell, Gloria T.
    Liu, Yajuan J.
    Chen, Hui
    Chen, Beiyun
    Meyer, Reid G.
    Yuhas, Jason A.
    Geiersbach, Katherine B.
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2018, 149 (02) : 135 - 147
  • [39] Tissue microarray technology in the routine assessment of HER2 status in invasive breast cancer
    Cryan, Jane
    O'Grady, Anthony
    Allen, David
    Kay, Elaine
    HISTOPATHOLOGY, 2009, 54 (07) : 901 - 901
  • [40] Resolving the ERBB2 (HER2) Status of Invasive Breast Cancers with Double-Equivocal HER2 Status by Immunohistochemistry and Fluorescence In-situ Hybridization
    Hon, Jane Date
    Zhang, Xinmin
    Edmonston, Tina Bocker
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2016, 146 : S96 - S96