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Performance of Oncomine Fusion Transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens
Gene fusions play an important role in the carcinogenesis of lung adenocarcinoma. The recent association of four oncogenic driver genes, ALK, ROS1, RET, and NTRK1, as lung tumor predictive biomarkers has increased the need for precision medicine. We used formalin‐fixed, paraffin‐embedded tissue samp...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549924/ https://www.ncbi.nlm.nih.gov/pubmed/30972901 http://dx.doi.org/10.1111/cas.14016 |
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author | Sakai, Kazuko Ohira, Tatsuo Matsubayashi, Jun Yoneshige, Azusa Ito, Akihiko Mitsudomi, Tetsuya Nagao, Toshitaka Iwamatsu, Emi Katayama, Jin Ikeda, Norihiko Nishio, Kazuto |
author_facet | Sakai, Kazuko Ohira, Tatsuo Matsubayashi, Jun Yoneshige, Azusa Ito, Akihiko Mitsudomi, Tetsuya Nagao, Toshitaka Iwamatsu, Emi Katayama, Jin Ikeda, Norihiko Nishio, Kazuto |
author_sort | Sakai, Kazuko |
collection | PubMed |
description | Gene fusions play an important role in the carcinogenesis of lung adenocarcinoma. The recent association of four oncogenic driver genes, ALK, ROS1, RET, and NTRK1, as lung tumor predictive biomarkers has increased the need for precision medicine. We used formalin‐fixed, paraffin‐embedded tissue samples of non‐small cell lung cancer from 150 EGFR mutation‐negative cases and 10 fusion status‐known cases and compared the performance of the Oncomine Dx Fusion Transcript Test (ODxFT) with FISH break‐apart for the detection of ALK, RET, and ROS1 fusion genes. RNA was extracted from the paraffin‐embedded tissue samples with or without macrodissection under hematoxylin and eosin staining, and the ALK fusion gene was independently determined using these assays. Fusion detection analyses were successfully carried out using ODxFT in 150 cases, with only one invalid case. ALK fusion genes were detected at a frequency of 7.3% (11/150) in the lung cancer specimens. Concordance rate between the ODxFT and ALK‐FISH analyses was 99.3% (148/149). Sensitivity and specificity were 91.7% and 99.3%, respectively. All the samples with a known fusion status were accurately matched between the two assays. Our results show a high concordance rate between the ODxFT and ALK‐FISH analyses. ODxFT was thus validated as an effective method for detecting clinically significant ALK fusion genes in paraffin‐embedded tissue samples. |
format | Online Article Text |
id | pubmed-6549924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65499242019-06-07 Performance of Oncomine Fusion Transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens Sakai, Kazuko Ohira, Tatsuo Matsubayashi, Jun Yoneshige, Azusa Ito, Akihiko Mitsudomi, Tetsuya Nagao, Toshitaka Iwamatsu, Emi Katayama, Jin Ikeda, Norihiko Nishio, Kazuto Cancer Sci Original Articles Gene fusions play an important role in the carcinogenesis of lung adenocarcinoma. The recent association of four oncogenic driver genes, ALK, ROS1, RET, and NTRK1, as lung tumor predictive biomarkers has increased the need for precision medicine. We used formalin‐fixed, paraffin‐embedded tissue samples of non‐small cell lung cancer from 150 EGFR mutation‐negative cases and 10 fusion status‐known cases and compared the performance of the Oncomine Dx Fusion Transcript Test (ODxFT) with FISH break‐apart for the detection of ALK, RET, and ROS1 fusion genes. RNA was extracted from the paraffin‐embedded tissue samples with or without macrodissection under hematoxylin and eosin staining, and the ALK fusion gene was independently determined using these assays. Fusion detection analyses were successfully carried out using ODxFT in 150 cases, with only one invalid case. ALK fusion genes were detected at a frequency of 7.3% (11/150) in the lung cancer specimens. Concordance rate between the ODxFT and ALK‐FISH analyses was 99.3% (148/149). Sensitivity and specificity were 91.7% and 99.3%, respectively. All the samples with a known fusion status were accurately matched between the two assays. Our results show a high concordance rate between the ODxFT and ALK‐FISH analyses. ODxFT was thus validated as an effective method for detecting clinically significant ALK fusion genes in paraffin‐embedded tissue samples. John Wiley and Sons Inc. 2019-05-03 2019-06 /pmc/articles/PMC6549924/ /pubmed/30972901 http://dx.doi.org/10.1111/cas.14016 Text en © 2019 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Sakai, Kazuko Ohira, Tatsuo Matsubayashi, Jun Yoneshige, Azusa Ito, Akihiko Mitsudomi, Tetsuya Nagao, Toshitaka Iwamatsu, Emi Katayama, Jin Ikeda, Norihiko Nishio, Kazuto Performance of Oncomine Fusion Transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens |
title | Performance of Oncomine Fusion Transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens |
title_full | Performance of Oncomine Fusion Transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens |
title_fullStr | Performance of Oncomine Fusion Transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens |
title_full_unstemmed | Performance of Oncomine Fusion Transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens |
title_short | Performance of Oncomine Fusion Transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens |
title_sort | performance of oncomine fusion transcript kit for formalin‐fixed, paraffin‐embedded lung cancer specimens |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549924/ https://www.ncbi.nlm.nih.gov/pubmed/30972901 http://dx.doi.org/10.1111/cas.14016 |
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