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Utilization of cytologic cell blocks for targeted sequencing of solid tumors

BACKGROUND: Targeted sequencing of cytologic samples has significantly increased in recent years. With increasing numbers of clinical trials for variant specific therapeutics, validating a comprehensive assay for cytologic samples has become clinically important. AIM: For this study, a retrospective...

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Autores principales: Vormittag‐Nocito, Erica, Kumar, Ravindra, Narayan, Kunwar Digvijay, Chen, Zhengjia, David, Odile, Behm, Frederick, Mohapatra, Gayatry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972011/
https://www.ncbi.nlm.nih.gov/pubmed/36125633
http://dx.doi.org/10.1002/cam4.5261
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author Vormittag‐Nocito, Erica
Kumar, Ravindra
Narayan, Kunwar Digvijay
Chen, Zhengjia
David, Odile
Behm, Frederick
Mohapatra, Gayatry
author_facet Vormittag‐Nocito, Erica
Kumar, Ravindra
Narayan, Kunwar Digvijay
Chen, Zhengjia
David, Odile
Behm, Frederick
Mohapatra, Gayatry
author_sort Vormittag‐Nocito, Erica
collection PubMed
description BACKGROUND: Targeted sequencing of cytologic samples has significantly increased in recent years. With increasing numbers of clinical trials for variant specific therapeutics, validating a comprehensive assay for cytologic samples has become clinically important. AIM: For this study, a retrospective review of cytologic cell blocks from fine needle aspirations and fluid specimens was performed. METHODS: Two hundred twenty six total cases of solid tumor malignancies were identified, of which 120 cases and 20 lymph node negative controls were sequenced for the Oncomine Comprehensive Assay. Cytology and surgical specimen correlation was performed in a subset of cases. Statistical analysis to determine variant concordance was performed. RESULTS: Within the 117 cases sequenced, a total of 347 pathogenic variants were detected. Of the 117 cases, 32 cases (27.4%) would qualify for FDA approved targeted therapy according to the current guidelines, and an additional 23 cases (19.7%) would qualify for clinical trial based on pathogenic variants detected. DISCUSSION: With over 27% of cases in our cohort qualifying for some form of targeted therapy, our study shows the importance of providing comprehensive molecular diagnostic options. Despite only half of the cytology cases in the review period having enough material to be sequenced, overall approximately 27% of patients in this cohort would have benefitted from this service.
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spelling pubmed-99720112023-03-01 Utilization of cytologic cell blocks for targeted sequencing of solid tumors Vormittag‐Nocito, Erica Kumar, Ravindra Narayan, Kunwar Digvijay Chen, Zhengjia David, Odile Behm, Frederick Mohapatra, Gayatry Cancer Med RESEARCH ARTICLES BACKGROUND: Targeted sequencing of cytologic samples has significantly increased in recent years. With increasing numbers of clinical trials for variant specific therapeutics, validating a comprehensive assay for cytologic samples has become clinically important. AIM: For this study, a retrospective review of cytologic cell blocks from fine needle aspirations and fluid specimens was performed. METHODS: Two hundred twenty six total cases of solid tumor malignancies were identified, of which 120 cases and 20 lymph node negative controls were sequenced for the Oncomine Comprehensive Assay. Cytology and surgical specimen correlation was performed in a subset of cases. Statistical analysis to determine variant concordance was performed. RESULTS: Within the 117 cases sequenced, a total of 347 pathogenic variants were detected. Of the 117 cases, 32 cases (27.4%) would qualify for FDA approved targeted therapy according to the current guidelines, and an additional 23 cases (19.7%) would qualify for clinical trial based on pathogenic variants detected. DISCUSSION: With over 27% of cases in our cohort qualifying for some form of targeted therapy, our study shows the importance of providing comprehensive molecular diagnostic options. Despite only half of the cytology cases in the review period having enough material to be sequenced, overall approximately 27% of patients in this cohort would have benefitted from this service. John Wiley and Sons Inc. 2022-09-20 /pmc/articles/PMC9972011/ /pubmed/36125633 http://dx.doi.org/10.1002/cam4.5261 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Vormittag‐Nocito, Erica
Kumar, Ravindra
Narayan, Kunwar Digvijay
Chen, Zhengjia
David, Odile
Behm, Frederick
Mohapatra, Gayatry
Utilization of cytologic cell blocks for targeted sequencing of solid tumors
title Utilization of cytologic cell blocks for targeted sequencing of solid tumors
title_full Utilization of cytologic cell blocks for targeted sequencing of solid tumors
title_fullStr Utilization of cytologic cell blocks for targeted sequencing of solid tumors
title_full_unstemmed Utilization of cytologic cell blocks for targeted sequencing of solid tumors
title_short Utilization of cytologic cell blocks for targeted sequencing of solid tumors
title_sort utilization of cytologic cell blocks for targeted sequencing of solid tumors
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972011/
https://www.ncbi.nlm.nih.gov/pubmed/36125633
http://dx.doi.org/10.1002/cam4.5261
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