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
  • [41] HER2 status and disparities in luminal breast cancers
    Holowatyj, Andreana N.
    Ruterbusch, Julie J.
    Ratnam, Manohar
    Gorski, David H.
    Cote, Michele L.
    CANCER MEDICINE, 2016, 5 (08): : 2109 - 2116
  • [42] Establishment and evaluation of digital PCR methods for HER2 copy number variation in breast cancer
    Wang, Xia
    Xing, Dechun
    Liu, Zheng
    Zhang, Yujing
    Cheng, Bo
    Sun, Suozhu
    Wang, Qingtao
    Dong, Lianhua
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2023, 415 (04) : 725 - 733
  • [43] HER2 Gene Protein Assay: A Robust Tool for Evaluating HER2 Status and Intratumoral Heterogeneity in Endometrial Cancers
    Shafi, Saba
    Nitta, Hiroaki
    Shah, Manan
    Challa, Bindu
    Parwani, Anil, V
    Li, Zaibo
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2023, 159 (05) : 464 - 473
  • [44] HER2 status in breast cancer: changes in guidelines and complicating factors for interpretation
    Ahn, Soomin
    Woo, Ji Won
    Lee, Kyoungyul
    Park, So Yeon
    JOURNAL OF PATHOLOGY AND TRANSLATIONAL MEDICINE, 2020, 54 (01) : 34 - 44
  • [45] Whether to determine HER2 status for breast cancer in the primary tumour or in the metastasis
    Santiago, M. P.
    Vazquez-Boquete, A.
    Fernandez, B.
    Masa, C.
    Antunez, J. R.
    Fraga, M.
    Forteza, J.
    Garcia-Caballero, T.
    HISTOLOGY AND HISTOPATHOLOGY, 2009, 24 (06) : 675 - 682
  • [46] 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
  • [47] Impact of chromosome 17 centromere copy number increase on patient survival and human epidermal growth factor receptor 2 expression in gastric adenocarcinoma
    Ciesielski, Maciej
    Szajewski, Mariusz
    Walczak, Jakub
    Peksa, Rafal
    Lenckowski, Radoslaw
    Supel, Malgorzata
    Zielinski, Jacek
    Kruszewski, Wieslaw Janusz
    ONCOLOGY LETTERS, 2021, 21 (02)
  • [48] Breast Cancer With HER2 Immunohistochemical Score 2 and Average HER2 Signals/Cell 6 or More and HER2/CEP17 Ratio Less Than 2 ('ISH Group 3'): A Multiinstitutional Cohort Analysis Emphasizing Outcome and Molecular Subtype
    Ajabnoor, Rana
    Zhang, Gloria
    Hu, Yan
    Gao, Yuan
    Finkelman, Brian S.
    Turner, Bradley M.
    Yi, Sha
    Dhakal, Ajay
    Audeh, William
    Li, Zaibo
    Li, Xiaoxian
    Hicks, David G.
    Zhang, Huina
    MODERN PATHOLOGY, 2024, 37 (08)
  • [49] Clinical array-based karyotyping of breast cancer with equivocal HER2 status resolves gene copy number and reveals chromosome 17 complexity
    Gunn, Shelly
    Yeh, I-Tien
    Lytvak, Irina
    Tirtorahardjo, Budi
    Dzidic, Natasha
    Zadeh, Soheila
    Kim, Jaeweon
    McCaskill, Chris
    Lim, Lony
    Gorre, Mercedes
    Mohammed, Mansoor
    BMC CANCER, 2010, 10
  • [50] Monosomy of chromosome 17 in breast cancer during interpretation of HER2 gene amplification
    Brunelli, Matteo
    Nottegar, Alessia
    Bogina, Giuseppe
    Calio, Anna
    Cima, Luca
    Eccher, Albino
    Vicentini, Caterina
    Marcolini, Lisa
    Scarpa, Aldo
    Pedron, Serena
    Brunello, Eleonora
    Knuutila, Sakari
    Sapino, Anna
    Marchio, Caterina
    Bria, Emilio
    Molino, Annamaria
    Carbognin, Luisa
    Tortora, Giampaolo
    Jasani, Bharat
    Miller, Keith
    Merdol, Ibrahim
    Zanatta, Lucia
    Laurino, Licia
    Wirtanen, Tiina
    Zamboni, Giuseppe
    Marconi, Marcella
    Chilosi, Marco
    Manfrin, Erminia
    Martignoni, Guido
    Bonetti, Franco
    AMERICAN JOURNAL OF CANCER RESEARCH, 2015, 5 (07): : 2212 - 2221