Cargando…
Deviating HER2 test results in gastric cancer: analysis from the prospective multicenter VARIANZ study
PURPOSE: The prospective multicenter VARIANZ study aimed to identify resistance biomarkers for HER2-targeted treatment in advanced gastric and esophago-gastric junction cancer (GC, EGJC). HER2 test deviations were found in 90 (22.3%) of 404 cases (central versus local testing) and were associated wi...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984518/ https://www.ncbi.nlm.nih.gov/pubmed/36030286 http://dx.doi.org/10.1007/s00432-022-04208-6 |
_version_ | 1784900762131759104 |
---|---|
author | Kolbe, Katharina Haffner, Ivonne Schierle, Katrin Maier, Dieter Geier, Birgitta Luber, Birgit Bläker, Hendrik Wittekind, Christian Lordick, Florian |
author_facet | Kolbe, Katharina Haffner, Ivonne Schierle, Katrin Maier, Dieter Geier, Birgitta Luber, Birgit Bläker, Hendrik Wittekind, Christian Lordick, Florian |
author_sort | Kolbe, Katharina |
collection | PubMed |
description | PURPOSE: The prospective multicenter VARIANZ study aimed to identify resistance biomarkers for HER2-targeted treatment in advanced gastric and esophago-gastric junction cancer (GC, EGJC). HER2 test deviations were found in 90 (22.3%) of 404 cases (central versus local testing) and were associated with negative impact on survival for trastuzumab-treated patients. Here, we investigated methodological and biological variables that may promote deviating HER2 test results. METHODS: We analyzed HER2 testing procedures and participation in quality assurance programs of 105 participating local pathology laboratories. Furthermore, tumor localization and histological subtypes were compared between patients with centrally confirmed (central HER2 + /local HER2 + , n = 68) and unconfirmed HER2 status (central HER2 −/local HER2 + , n = 68). RESULTS: For central HER2 testing, concordance between in situ hybridization (ISH) and immunohistochemistry (IHC) was 98.3%, with IHC sensitivity of 93.3% (84 IHC + of 90 ISH +), specificity of 99.5% (389 IHC- of 391 ISH-), and a positive diagnosis rate of 97.7%. Central confirmation of the local HER2 IHC scores were seen for the majority of locally HER2- IHC 0/1 (172/178; 96.6%), but less frequently for locally IHC3 + (57/124; 46.0%) cases. Deviation rate was not associated with IHC antibody platform used in the local pathology institute neither with participation in quality-assuring tests. Regarding tumor characteristics, deviating test results were more frequently found in GC vs. EGJC (69.1% vs. 39.7%; p = 0.001) and in Laurén diffuse vs. intestinal subtype (23.5% vs. 5.9%, p = 0.004). CONCLUSION: Tumor localization and histological subtype have an impact on HER2 test deviation rates. Assessment of HER2 remains challenging for GC and EGJC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-022-04208-6. |
format | Online Article Text |
id | pubmed-9984518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-99845182023-03-05 Deviating HER2 test results in gastric cancer: analysis from the prospective multicenter VARIANZ study Kolbe, Katharina Haffner, Ivonne Schierle, Katrin Maier, Dieter Geier, Birgitta Luber, Birgit Bläker, Hendrik Wittekind, Christian Lordick, Florian J Cancer Res Clin Oncol Research PURPOSE: The prospective multicenter VARIANZ study aimed to identify resistance biomarkers for HER2-targeted treatment in advanced gastric and esophago-gastric junction cancer (GC, EGJC). HER2 test deviations were found in 90 (22.3%) of 404 cases (central versus local testing) and were associated with negative impact on survival for trastuzumab-treated patients. Here, we investigated methodological and biological variables that may promote deviating HER2 test results. METHODS: We analyzed HER2 testing procedures and participation in quality assurance programs of 105 participating local pathology laboratories. Furthermore, tumor localization and histological subtypes were compared between patients with centrally confirmed (central HER2 + /local HER2 + , n = 68) and unconfirmed HER2 status (central HER2 −/local HER2 + , n = 68). RESULTS: For central HER2 testing, concordance between in situ hybridization (ISH) and immunohistochemistry (IHC) was 98.3%, with IHC sensitivity of 93.3% (84 IHC + of 90 ISH +), specificity of 99.5% (389 IHC- of 391 ISH-), and a positive diagnosis rate of 97.7%. Central confirmation of the local HER2 IHC scores were seen for the majority of locally HER2- IHC 0/1 (172/178; 96.6%), but less frequently for locally IHC3 + (57/124; 46.0%) cases. Deviation rate was not associated with IHC antibody platform used in the local pathology institute neither with participation in quality-assuring tests. Regarding tumor characteristics, deviating test results were more frequently found in GC vs. EGJC (69.1% vs. 39.7%; p = 0.001) and in Laurén diffuse vs. intestinal subtype (23.5% vs. 5.9%, p = 0.004). CONCLUSION: Tumor localization and histological subtype have an impact on HER2 test deviation rates. Assessment of HER2 remains challenging for GC and EGJC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-022-04208-6. Springer Berlin Heidelberg 2022-08-27 2023 /pmc/articles/PMC9984518/ /pubmed/36030286 http://dx.doi.org/10.1007/s00432-022-04208-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Kolbe, Katharina Haffner, Ivonne Schierle, Katrin Maier, Dieter Geier, Birgitta Luber, Birgit Bläker, Hendrik Wittekind, Christian Lordick, Florian Deviating HER2 test results in gastric cancer: analysis from the prospective multicenter VARIANZ study |
title | Deviating HER2 test results in gastric cancer: analysis from the prospective multicenter VARIANZ study |
title_full | Deviating HER2 test results in gastric cancer: analysis from the prospective multicenter VARIANZ study |
title_fullStr | Deviating HER2 test results in gastric cancer: analysis from the prospective multicenter VARIANZ study |
title_full_unstemmed | Deviating HER2 test results in gastric cancer: analysis from the prospective multicenter VARIANZ study |
title_short | Deviating HER2 test results in gastric cancer: analysis from the prospective multicenter VARIANZ study |
title_sort | deviating her2 test results in gastric cancer: analysis from the prospective multicenter varianz study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984518/ https://www.ncbi.nlm.nih.gov/pubmed/36030286 http://dx.doi.org/10.1007/s00432-022-04208-6 |
work_keys_str_mv | AT kolbekatharina deviatingher2testresultsingastriccanceranalysisfromtheprospectivemulticentervarianzstudy AT haffnerivonne deviatingher2testresultsingastriccanceranalysisfromtheprospectivemulticentervarianzstudy AT schierlekatrin deviatingher2testresultsingastriccanceranalysisfromtheprospectivemulticentervarianzstudy AT maierdieter deviatingher2testresultsingastriccanceranalysisfromtheprospectivemulticentervarianzstudy AT geierbirgitta deviatingher2testresultsingastriccanceranalysisfromtheprospectivemulticentervarianzstudy AT luberbirgit deviatingher2testresultsingastriccanceranalysisfromtheprospectivemulticentervarianzstudy AT blakerhendrik deviatingher2testresultsingastriccanceranalysisfromtheprospectivemulticentervarianzstudy AT wittekindchristian deviatingher2testresultsingastriccanceranalysisfromtheprospectivemulticentervarianzstudy AT lordickflorian deviatingher2testresultsingastriccanceranalysisfromtheprospectivemulticentervarianzstudy |