HER2/neu Gene Amplification Heterogeneity: The Significance of Cells With a 3:1 HER2/CEP17 Ratio

被引:3
作者
Layfield, Lester J. [1 ,2 ]
Schmidt, Robert L. [1 ]
机构
[1] Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USA
[2] ARUP Labs, Salt Lake City, UT USA
关键词
HER2/neu; amplification; heterogeneity; breast carcinoma; IN-SITU HYBRIDIZATION; BREAST-CANCER; INTRATUMORAL HETEROGENEITY; CARCINOMAS;
D O I
10.1097/PAI.0b013e31824d04e8
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
College of American Pathologists published guidelines for the assessment of HER2/neu genetic heterogeneity. When 20 cells are counted for evaluation of HER2/neu amplification, a single 3:1 HER2/CEP17 ratio cell characterizes the sample as heterogneous. Heterogeneity for HER2/neu amplification may indicate biologically important characteristics including likelihood of amplification in metastases. We performed fluorescence in situ hybridization on 1546 cases. For each case, 20 cells of invasive carcinoma were analyzed for HER2/CEP17 ratio. Cases were assessed as nonamplified (ratio < 1.8), borderline amplified (1.8 <= ratio <= 2.2), or amplified (ratio > 2.20). Heterogeneity was present when the percentage of cell with ratios > 2.20 was >= 5% but < 50%. Individual cells were typed by probe ratios and distribution of cell types determined. The distribution of HER2/CEP17 ratio was determined with the number of 3:1 HER2/CEP17 cells plotted against the number of amplified cells. 3:1 HER2/CEP17 ratio cells occur with low frequency (2.2%) but are the determining factor for heterogeneity in 46% of heterogenous cases. Thirty-five percent of heterogenous cases were due to a single 3:1 cell. Single 3:1 cells are a poor predictor for additional amplified cells. Inclusion of cells with a 3:1 HER2/CEP17 ratio in the definition of heterogeneity may be too broad as these cells are the determining factor in approximately one third of diagnoses of heterogeneity but are not strongly associated with other measures of amplification. Moreover, 3:1 HER2/CEP17 ratio cells are a poor predictor for the presence of additional amplified cells in a sample.
引用
收藏
页码:543 / 549
页数:7
相关论文
共 14 条
[1]   Heterogeneous HER2 Gene Amplification Impact on Patient Outcome and a Clinically Relevant Definition [J].
Bartlett, Alastair I. ;
Starcyznski, Jane ;
Robson, Tammy ;
MacLellan, Alex ;
Campbell, Fiona M. ;
van de Vekle, Cornelis J. H. ;
Hasenburg, Annette ;
Markopoulos, Christos ;
Seynaeve, Caroline ;
Rea, Daniel ;
Bartlett, John M. S. .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2011, 136 (02) :266-274
[2]   The complexity of genotype alterations underlying HER2-positive by breast cancer: an explanation for its clinical heterogeneity [J].
Bempt, Isabelle Vanden ;
Drijkoningen, Maria ;
De Wolf-Peeters, Christiane .
CURRENT OPINION IN ONCOLOGY, 2007, 19 (06) :552-557
[3]  
Farabegoli F, 2001, CYTOMETRY, V46, P50, DOI 10.1002/1097-0320(20010215)46:1<50::AID-CYTO1037>3.0.CO
[4]  
2-T
[5]   Marked intratumoral heterogeneity of c-myc and CyclinD1 but not of c-erbB2 amplification in breast cancer [J].
Glöckner, S ;
Buurman, H ;
Kleeberger, W ;
Lehmann, U ;
Kreipe, H .
LABORATORY INVESTIGATION, 2002, 82 (10) :1419-1426
[6]  
Hsu CY, 2010, ARCH PATHOL LAB MED, V134, P162, DOI 10.1043/1543-2165-134.2.162.a
[7]   HER-2 testing in breast cancer using immunohistochemical analysis and fluorescence in situ hybridization - A single-institution experience of 2,279 cases and comparison of dual-color and single-color scoring [J].
Lal, P ;
Salazar, PA ;
Hudis, CA ;
Ladanyi, M ;
Chen, BY .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2004, 121 (05) :631-636
[8]   Analysis of intratumoral heterogeneity and amplification status in breast carcinomas with equivocal (2+) HER-2 immunostaining [J].
Lewis, JT ;
Ketterling, RP ;
Halling, KC ;
Reynolds, C ;
Jenkins, RB ;
Visscher, DW .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2005, 124 (02) :273-281
[9]  
Malowany JI, 2011, MOD PATHOL A, V53A
[10]  
Owens Marilyn A, 2004, Clin Breast Cancer, V5, P63, DOI 10.3816/CBC.2004.n.011