Heterogeneous HER2 Gene Amplification Impact on Patient Outcome and a Clinically Relevant Definition

被引:97
作者
Bartlett, Alastair I. [1 ]
Starcyznski, Jane [2 ]
Robson, Tammy [1 ]
MacLellan, Alex [3 ]
Campbell, Fiona M. [1 ]
van de Vekle, Cornelis J. H. [4 ]
Hasenburg, Annette [5 ]
Markopoulos, Christos [6 ]
Seynaeve, Caroline [7 ]
Rea, Daniel [8 ]
Bartlett, John M. S. [1 ]
机构
[1] Univ Edinburgh, Endocrine Canc Grp, Edinburgh, Midlothian, Scotland
[2] Birmingham Heartlands Hosp, Dept Pathol, Birmingham B9 5ST, W Midlands, England
[3] Univ Edinburgh, Expt Canc Med Ctr, Edinburgh, Midlothian, Scotland
[4] Leiden Univ, Med Ctr, Leiden, Netherlands
[5] Univ Hosp, Freiburg, Germany
[6] Univ Athens, Sch Med, GR-11527 Athens, Greece
[7] Erasmus MC, Dept Med Oncol, Rotterdam, Netherlands
[8] Univ Birmingham, Canc Res UK Clin Trials Unit, Birmingham B15 2TT, W Midlands, England
关键词
HER2; Amplification; Breast; Heterogeneity; BREAST-CANCER; ADJUVANT CHEMOTHERAPY; RECOMMENDATIONS; RECEPTOR; CHROMOSOME-17; TAMOXIFEN; UK;
D O I
10.1309/AJCP0EN6AQMWETZZ
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
Heterogeneous expression or amplification is a challenge to HER2 diagnostics. A guideline defines heterogeneity as the presence of between 5% and 50% cells with HER2/CEP17 ratios of more than 2.20. We audited the frequency of such cells and their clinical impact in the results from 2 pathology laboratories combined with data from the TEAM [Tamoxifen vs Exemestane Adjuvant Multicentre] pathology study. HER2 reports were scanned and the percentages of amplified cells reported. Of 6,461 eligible cases, 754 (11.7%) exhibited 50% or more cells with ratios of more than 2.20, which is "amplified" by College of American Pathologists guidelines. Of the cases, 2,166 (33.5%) exhibited more than 5% but less than 50% of cells with HER2/CEP17 ratios of more than 2.20, or "heterogeneous amplification." No prognostic impact was observed when fewer than 30% of cells exhibited ratios of more than 2.20. All amplified cases with 30% to 50% of cells with ratios more than 2.20 were identified as such by United Kingdom guidelines. The percentage of tumor cells with HER2/CEP17 ratios more than 2.20 does not identify cases with heterogeneous amplification or poor outcome. A modified approach for identification of true heterogeneous amplification is suggested.
引用
收藏
页码:266 / 274
页数:9
相关论文
共 22 条
[1]
[Anonymous], 2007, J CLIN ONCOL, DOI DOI 10.1200/JCO.2006.09.2775
[2]
[Anonymous], 2007, CURR DIAGN PATHOL
[3]
Determination of HER2 Amplification by In Situ Hybridization: When Should Chromosome 17 also be Determined? [J].
Bartlett, John M. S. ;
Campbell, Fiona M. ;
Mallon, Elizabeth A. .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2008, 130 (06) :920-926
[4]
Estrogen Receptor and Progesterone Receptor As Predictive Biomarkers of Response to Endocrine Therapy: A Prospectively Powered Pathology Study in the Tamoxifen and Exemestane Adjuvant Multinational Trial [J].
Bartlett, John M. S. ;
Brookes, Cassandra L. ;
Robson, Tammy ;
van de Velde, Cornelis J. H. ;
Billingham, Lucinda J. ;
Campbell, Fiona M. ;
Grant, Margaret ;
Hasenburg, Annette ;
Hille, Elysee T. M. ;
Kay, Charlene ;
Kieback, Dirk G. ;
Putter, Hein ;
Markopoulos, Christos ;
Kranenbarg, Elma Meershoek-Klein ;
Mallon, Elizabeth A. ;
Dirix, Luc ;
Seynaeve, Caroline ;
Rea, Daniel .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (12) :1531-1538
[5]
Predictive markers of anthracycline benefit: a prospectively planned analysis of the UK National Epirubicin Adjuvant Trial (NEAT/BR9601) [J].
Bartlett, John M. S. ;
Munro, Alison F. ;
Dunn, Janet A. ;
McConkey, Christopher ;
Jordan, Sarah ;
Twelves, Chris J. ;
Cameron, David A. ;
Thomas, Jeremy ;
Campbell, Fiona M. ;
Rea, Daniel W. ;
Provenzano, Elena ;
Caldas, Carlos ;
Pharaoh, Paul ;
Hiller, Louise ;
Earl, Helena ;
Poole, Christopher J. .
LANCET ONCOLOGY, 2010, 11 (03) :266-274
[6]
External Quality Assurance of HER2 FISH and ISH Testing Three Years of the UK National External Quality Assurance Scheme [J].
Bartlett, John M. S. ;
Ibrahim, Merdol ;
Jasani, Bharat ;
Morgan, John M. ;
Ellis, Ian ;
Kay, Elaine ;
Connolly, Yvonne ;
Campbell, Fiona ;
O'Grady, Anthony ;
Barnett, Sarah ;
Miller, Keith .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2009, 131 (01) :106-111
[7]
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
[8]
Current perspectives on HER2 testing:: A review of national testing guidelines [J].
Bilous, M ;
Dowsett, M ;
Hanna, W ;
Isola, J ;
Lebeau, A ;
Moreno, A ;
Penault-Llorca, F ;
Rüschoff, J ;
Tomasic, G ;
de Vijver, MV .
MODERN PATHOLOGY, 2003, 16 (02) :173-182
[9]
HER2 testing recommendations in Australia [J].
Bilous, M .
PATHOLOGY, 2001, 33 (04) :425-427
[10]
Recommendations for HER2 testing in the UK [J].
Ellis, IO ;
Dowsett, M ;
Bartlett, J ;
Walker, R ;
Cooke, T ;
Gullick, W ;
Gusterson, B ;
Mallon, E ;
Lee, PB .
JOURNAL OF CLINICAL PATHOLOGY, 2000, 53 (12) :890-892