Literature DB >> 22389512

Predictors of human epidermal growth factor receptor 2 fluorescence in-situ hybridisation amplification in immunohistochemistry score 2+ infiltrating breast cancer: a single institution analysis.

Maria Vittoria Dieci1, Elena Barbieri, Stefania Bettelli, Federico Piacentini, Claudia Omarini, Guido Ficarra, Sara Balduzzi, Massimo Dominici, Pierfranco Conte, Valentina Guarneri.   

Abstract

AIMS: Eligibility for anti-human epidermal growth factor receptor 2 (HER2) treatments in breast cancer requires a correct HER2 status assessment. Testing guidelines recommend fluorescence in-situ hybridisation (FISH) for samples scored as 2+ by immunohistochemistry. This study investigates the correlation between pathological features and FISH amplification in HER2 2+ breast cancer cases.
METHODS: 480 HER2 2+ breast cancer samples were included. The association between tumour grade, hormone receptor status, proliferation index (Ki67) and FISH amplification, using both US Food and Drug Administration (ratio ≥2) and American Society of Clinical Oncologists/College of American Pathologists cut-offs (ratio >2.2) was evaluated.
RESULTS: 90.2% of the samples were hormone receptor positive. The median Ki67 value was 23.5%; 311 (64.8%) samples showed a Ki67 value of 15% or greater. Tumour grade was evaluable in 421 cases (87.7%), 268 (55.8%) being grade 3. FISH amplification rates were 27.5% (ratio ≥2.0) and 20.8% (ratio >2.2). Grade 3 tumours were more frequently amplified than grades 1-2 tumours: 34% versus 18% (ratio ≥2.0, p<0.001) and 27% versus 9% (ratio >2.2, p<0.001). Samples with Ki67 of 15% or greater showed higher amplification rates than low Ki67 samples: 31% versus 21% (ratio ≥2.0, p=0.022) and 25% versus 12% (ratio >2.2, p=0.003). The OR for FISH amplification was significant in the case of grade 3 and high Ki67 with both cut-offs.
CONCLUSIONS: In this study, high tumour grade and high Ki67 significantly predicted FISH amplification in 480 HER2 2+ breast cancer samples.

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Year:  2012        PMID: 22389512     DOI: 10.1136/jclinpath-2011-200643

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  5 in total

1.  Gene status in HER2 equivocal breast carcinomas: impact of distinct recommendations and contribution of a polymerase chain reaction-based method.

Authors:  Anna Sapino; Francesca Maletta; Ludovica Verdun di Cantogno; Luigia Macrì; Cristina Botta; Patrizia Gugliotta; Maria Stella Scalzo; Laura Annaratone; Davide Balmativola; Francesca Pietribiasi; Paolo Bernardi; Riccardo Arisio; Laura Viberti; Stefano Guzzetti; Renzo Orlassino; Cristiana Ercolani; Marcella Mottolese; Giuseppe Viale; Caterina Marchiò
Journal:  Oncologist       Date:  2014-10-16

2.  Clinicopathological variables predicting HER-2 gene status in immunohistochemistry-equivocal (2+) invasive breast cancer.

Authors:  Yongling Ji; Liming Sheng; Xianghui Du; Guoqin Qiu; Bo Chen; Xiaojia Wang
Journal:  J Thorac Dis       Date:  2014-07       Impact factor: 2.895

3.  Unraveling the chromosome 17 patterns of FISH in interphase nuclei: an in-depth analysis of the HER2 amplicon and chromosome 17 centromere by karyotyping, FISH and M-FISH in breast cancer cells.

Authors:  Milena Rondón-Lagos; Ludovica Verdun Di Cantogno; Nelson Rangel; Teresa Mele; Sandra R Ramírez-Clavijo; Giorgio Scagliotti; Caterina Marchiò; Anna Sapino
Journal:  BMC Cancer       Date:  2014-12-07       Impact factor: 4.430

4.  Changes in Pathological Complete Response Rates after Neoadjuvant Chemotherapy for Breast Carcinoma over Five Years.

Authors:  Daniel C McFarland; Jessica Naikan; Mariya Rozenblit; John Mandeli; Ira Bleiweiss; Amy Tiersten
Journal:  J Oncol       Date:  2016-06-13       Impact factor: 4.375

5.  Evaluation of Immunohistochemistry-Equivocal (2+) HER2 Gene Status in Invasive Breast Cancer by Silver DNA in Situ Hybridization (SISH) and its Association with Clinicopathological Variables.

Authors:  Zaidoon A Musa; Ban J Qasim; A Wahab A K Al Shaikhly
Journal:  Iran J Pathol       Date:  2016-08-30
  5 in total

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