author_facet Ma, Yan
Lespagnard, Laurence
Durbecq, Virginie
Paesmans, Marianne
Desmedt, Christine
Gomez-Galdon, Maria
Veys, Isabelle
Cardoso, Fatima
Sotiriou, Christos
Di Leo, Angelo
Piccart, Martine J.
Larsimont, Denis
Ma, Yan
Lespagnard, Laurence
Durbecq, Virginie
Paesmans, Marianne
Desmedt, Christine
Gomez-Galdon, Maria
Veys, Isabelle
Cardoso, Fatima
Sotiriou, Christos
Di Leo, Angelo
Piccart, Martine J.
Larsimont, Denis
author Ma, Yan
Lespagnard, Laurence
Durbecq, Virginie
Paesmans, Marianne
Desmedt, Christine
Gomez-Galdon, Maria
Veys, Isabelle
Cardoso, Fatima
Sotiriou, Christos
Di Leo, Angelo
Piccart, Martine J.
Larsimont, Denis
spellingShingle Ma, Yan
Lespagnard, Laurence
Durbecq, Virginie
Paesmans, Marianne
Desmedt, Christine
Gomez-Galdon, Maria
Veys, Isabelle
Cardoso, Fatima
Sotiriou, Christos
Di Leo, Angelo
Piccart, Martine J.
Larsimont, Denis
Clinical Cancer Research
Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
Cancer Research
Oncology
author_sort ma, yan
spelling Ma, Yan Lespagnard, Laurence Durbecq, Virginie Paesmans, Marianne Desmedt, Christine Gomez-Galdon, Maria Veys, Isabelle Cardoso, Fatima Sotiriou, Christos Di Leo, Angelo Piccart, Martine J. Larsimont, Denis 1078-0432 1557-3265 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1078-0432.ccr-04-2256 <jats:title>Abstract</jats:title> <jats:p>Purpose: To assess the effect of chromosome 17 copy number on HER-2/neu status determination in breast cancers.</jats:p> <jats:p>Experimental Design: HER-2/neu gene copy and chromosome 17 centromere numbers were evaluated on 893 breast carcinomas using double color fluorescence in situ hybridization (FISH). The net and chromosome 17 corrected (ratio) HER-2/neu copy numbers were compared and related to immunohistochemistry done according to the Food and Drug Administration (FDA)–approved scoring system (0, 1+, 2+, and 3+) as a first screening step in 584 cases.</jats:p> <jats:p>Results: When a ratio ≥2 was considered as criterion for FISH positivity, 49.3% (440 of 893) of cases showed amplification versus 56.2% (502 of 893) by using a net HER-2/neu gene copy number &amp;gt;4 as a alternative criterion; 14.8% (67 of 453) of cases having a ratio &amp;lt;2 had a net HER-2/neu gene copy number &amp;gt;4 and 1.1% (5 of 440) with a ratio ≥2 had a net HER-2/neu gene copy number &amp;lt;4. Among discordant cases, 88.8% (64 of 72) were polysomic (&amp;gt;2.25 chromosomes 17/cell) and among polysomic cases, 12.8% (40 of 312) of the low polysomic (2.26-3.75 chromosomes 17/cell) and 36.9% (24 of 65) of the highly polysomic (&amp;gt;3.75 chromosomes 17/cell) cases showed discordance. In cases with a ratio &amp;lt;2, polysomy 17 incidences were 85.7% (6 of 7) in IHC 3+, 42.4% (79 of 186) in IHC 2+, 33.3% (15 of 45) in IHC 1+, and 29.1% (16 of 55) in IHC 0.</jats:p> <jats:p>Conclusion: A net increase in HER-2/neu gene copy number consecutive to polysomy 17 in the absence of specific gene amplification might lead to a strong protein overexpression in a small subset of breast carcinomas. HER-2/neu status determination by FISH is dependent on the criterion considered for positivity in clinical practice.</jats:p> Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice Clinical Cancer Research
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series Clinical Cancer Research
source_id 49
title Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_unstemmed Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_full Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_fullStr Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_full_unstemmed Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_short Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_sort polysomy 17 in her-2/neu status elaboration in breast cancer: effect on daily practice
topic Cancer Research
Oncology
url http://dx.doi.org/10.1158/1078-0432.ccr-04-2256
publishDate 2005
physical 4393-4399
description <jats:title>Abstract</jats:title> <jats:p>Purpose: To assess the effect of chromosome 17 copy number on HER-2/neu status determination in breast cancers.</jats:p> <jats:p>Experimental Design: HER-2/neu gene copy and chromosome 17 centromere numbers were evaluated on 893 breast carcinomas using double color fluorescence in situ hybridization (FISH). The net and chromosome 17 corrected (ratio) HER-2/neu copy numbers were compared and related to immunohistochemistry done according to the Food and Drug Administration (FDA)–approved scoring system (0, 1+, 2+, and 3+) as a first screening step in 584 cases.</jats:p> <jats:p>Results: When a ratio ≥2 was considered as criterion for FISH positivity, 49.3% (440 of 893) of cases showed amplification versus 56.2% (502 of 893) by using a net HER-2/neu gene copy number &amp;gt;4 as a alternative criterion; 14.8% (67 of 453) of cases having a ratio &amp;lt;2 had a net HER-2/neu gene copy number &amp;gt;4 and 1.1% (5 of 440) with a ratio ≥2 had a net HER-2/neu gene copy number &amp;lt;4. Among discordant cases, 88.8% (64 of 72) were polysomic (&amp;gt;2.25 chromosomes 17/cell) and among polysomic cases, 12.8% (40 of 312) of the low polysomic (2.26-3.75 chromosomes 17/cell) and 36.9% (24 of 65) of the highly polysomic (&amp;gt;3.75 chromosomes 17/cell) cases showed discordance. In cases with a ratio &amp;lt;2, polysomy 17 incidences were 85.7% (6 of 7) in IHC 3+, 42.4% (79 of 186) in IHC 2+, 33.3% (15 of 45) in IHC 1+, and 29.1% (16 of 55) in IHC 0.</jats:p> <jats:p>Conclusion: A net increase in HER-2/neu gene copy number consecutive to polysomy 17 in the absence of specific gene amplification might lead to a strong protein overexpression in a small subset of breast carcinomas. HER-2/neu status determination by FISH is dependent on the criterion considered for positivity in clinical practice.</jats:p>
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author Ma, Yan, Lespagnard, Laurence, Durbecq, Virginie, Paesmans, Marianne, Desmedt, Christine, Gomez-Galdon, Maria, Veys, Isabelle, Cardoso, Fatima, Sotiriou, Christos, Di Leo, Angelo, Piccart, Martine J., Larsimont, Denis
author_facet Ma, Yan, Lespagnard, Laurence, Durbecq, Virginie, Paesmans, Marianne, Desmedt, Christine, Gomez-Galdon, Maria, Veys, Isabelle, Cardoso, Fatima, Sotiriou, Christos, Di Leo, Angelo, Piccart, Martine J., Larsimont, Denis, Ma, Yan, Lespagnard, Laurence, Durbecq, Virginie, Paesmans, Marianne, Desmedt, Christine, Gomez-Galdon, Maria, Veys, Isabelle, Cardoso, Fatima, Sotiriou, Christos, Di Leo, Angelo, Piccart, Martine J., Larsimont, Denis
author_sort ma, yan
container_issue 12
container_start_page 4393
container_title Clinical Cancer Research
container_volume 11
description <jats:title>Abstract</jats:title> <jats:p>Purpose: To assess the effect of chromosome 17 copy number on HER-2/neu status determination in breast cancers.</jats:p> <jats:p>Experimental Design: HER-2/neu gene copy and chromosome 17 centromere numbers were evaluated on 893 breast carcinomas using double color fluorescence in situ hybridization (FISH). The net and chromosome 17 corrected (ratio) HER-2/neu copy numbers were compared and related to immunohistochemistry done according to the Food and Drug Administration (FDA)–approved scoring system (0, 1+, 2+, and 3+) as a first screening step in 584 cases.</jats:p> <jats:p>Results: When a ratio ≥2 was considered as criterion for FISH positivity, 49.3% (440 of 893) of cases showed amplification versus 56.2% (502 of 893) by using a net HER-2/neu gene copy number &amp;gt;4 as a alternative criterion; 14.8% (67 of 453) of cases having a ratio &amp;lt;2 had a net HER-2/neu gene copy number &amp;gt;4 and 1.1% (5 of 440) with a ratio ≥2 had a net HER-2/neu gene copy number &amp;lt;4. Among discordant cases, 88.8% (64 of 72) were polysomic (&amp;gt;2.25 chromosomes 17/cell) and among polysomic cases, 12.8% (40 of 312) of the low polysomic (2.26-3.75 chromosomes 17/cell) and 36.9% (24 of 65) of the highly polysomic (&amp;gt;3.75 chromosomes 17/cell) cases showed discordance. In cases with a ratio &amp;lt;2, polysomy 17 incidences were 85.7% (6 of 7) in IHC 3+, 42.4% (79 of 186) in IHC 2+, 33.3% (15 of 45) in IHC 1+, and 29.1% (16 of 55) in IHC 0.</jats:p> <jats:p>Conclusion: A net increase in HER-2/neu gene copy number consecutive to polysomy 17 in the absence of specific gene amplification might lead to a strong protein overexpression in a small subset of breast carcinomas. HER-2/neu status determination by FISH is dependent on the criterion considered for positivity in clinical practice.</jats:p>
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spelling Ma, Yan Lespagnard, Laurence Durbecq, Virginie Paesmans, Marianne Desmedt, Christine Gomez-Galdon, Maria Veys, Isabelle Cardoso, Fatima Sotiriou, Christos Di Leo, Angelo Piccart, Martine J. Larsimont, Denis 1078-0432 1557-3265 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1078-0432.ccr-04-2256 <jats:title>Abstract</jats:title> <jats:p>Purpose: To assess the effect of chromosome 17 copy number on HER-2/neu status determination in breast cancers.</jats:p> <jats:p>Experimental Design: HER-2/neu gene copy and chromosome 17 centromere numbers were evaluated on 893 breast carcinomas using double color fluorescence in situ hybridization (FISH). The net and chromosome 17 corrected (ratio) HER-2/neu copy numbers were compared and related to immunohistochemistry done according to the Food and Drug Administration (FDA)–approved scoring system (0, 1+, 2+, and 3+) as a first screening step in 584 cases.</jats:p> <jats:p>Results: When a ratio ≥2 was considered as criterion for FISH positivity, 49.3% (440 of 893) of cases showed amplification versus 56.2% (502 of 893) by using a net HER-2/neu gene copy number &amp;gt;4 as a alternative criterion; 14.8% (67 of 453) of cases having a ratio &amp;lt;2 had a net HER-2/neu gene copy number &amp;gt;4 and 1.1% (5 of 440) with a ratio ≥2 had a net HER-2/neu gene copy number &amp;lt;4. Among discordant cases, 88.8% (64 of 72) were polysomic (&amp;gt;2.25 chromosomes 17/cell) and among polysomic cases, 12.8% (40 of 312) of the low polysomic (2.26-3.75 chromosomes 17/cell) and 36.9% (24 of 65) of the highly polysomic (&amp;gt;3.75 chromosomes 17/cell) cases showed discordance. In cases with a ratio &amp;lt;2, polysomy 17 incidences were 85.7% (6 of 7) in IHC 3+, 42.4% (79 of 186) in IHC 2+, 33.3% (15 of 45) in IHC 1+, and 29.1% (16 of 55) in IHC 0.</jats:p> <jats:p>Conclusion: A net increase in HER-2/neu gene copy number consecutive to polysomy 17 in the absence of specific gene amplification might lead to a strong protein overexpression in a small subset of breast carcinomas. HER-2/neu status determination by FISH is dependent on the criterion considered for positivity in clinical practice.</jats:p> Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice Clinical Cancer Research
spellingShingle Ma, Yan, Lespagnard, Laurence, Durbecq, Virginie, Paesmans, Marianne, Desmedt, Christine, Gomez-Galdon, Maria, Veys, Isabelle, Cardoso, Fatima, Sotiriou, Christos, Di Leo, Angelo, Piccart, Martine J., Larsimont, Denis, Clinical Cancer Research, Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice, Cancer Research, Oncology
title Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_full Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_fullStr Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_full_unstemmed Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_short Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
title_sort polysomy 17 in her-2/neu status elaboration in breast cancer: effect on daily practice
title_unstemmed Polysomy 17 in HER-2/neu Status Elaboration in Breast Cancer: Effect on Daily Practice
topic Cancer Research, Oncology
url http://dx.doi.org/10.1158/1078-0432.ccr-04-2256