Cargando…

Biomarker Testing for Patients With Advanced/Metastatic Nonsquamous NSCLC in the United States of America, 2015 to 2021

INTRODUCTION: NSCLC is a solid tumor with a growing number of actionable biomarkers that may inform treatment. Current guidelines recommend a broad, panel-based approach be taken to identify actionable markers. This retrospective study used a deidentified electronic health records database in the Un...

Descripción completa

Detalles Bibliográficos
Autores principales: Hess, Lisa M., Krein, Peter M., Haldane, Diane, Han, Yimei, Sireci, Anthony N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168140/
https://www.ncbi.nlm.nih.gov/pubmed/35677681
http://dx.doi.org/10.1016/j.jtocrr.2022.100336
_version_ 1784720935566180352
author Hess, Lisa M.
Krein, Peter M.
Haldane, Diane
Han, Yimei
Sireci, Anthony N.
author_facet Hess, Lisa M.
Krein, Peter M.
Haldane, Diane
Han, Yimei
Sireci, Anthony N.
author_sort Hess, Lisa M.
collection PubMed
description INTRODUCTION: NSCLC is a solid tumor with a growing number of actionable biomarkers that may inform treatment. Current guidelines recommend a broad, panel-based approach be taken to identify actionable markers. This retrospective study used a deidentified electronic health records database in the United States to evaluate utilization of various testing modalities. METHODS: Data from all adult patients diagnosed with having advanced/metastatic nonsquamous NSCLC between January 2015 and March 2021 were eligible if there was evidence of systemic therapy within 90 days of diagnosis. RESULTS: Records from a total of 17,513 patients (91.6% from community-based practices) were eligible with 83,064 genomic biomarker tests recorded from 2015 to 2021. The proportion of patients who received biomarker testing by next-generation sequencing (NGS)-based methods ranged from 28.3% in 2015 to 68.1% in 2020. The proportion of biomarker testing methods with inconclusive or unsuccessful results ranged from 3.4% for NGS to 9.7% for fluorescence in situ hybridization. The median time to receive results ranged from 4.0 days for polymerase chain reaction-based tests to 10.0 days for immunohistochemistry- and NGS-based tests. Median time to receive results was 8 days for academic and 9 days for community practices. CONCLUSIONS: These real-world data suggest increased adoption of NGS-based testing, yet nearly one-third of all patients with advanced/metastatic nonsquamous NSCLC still did not receive broad-based genomic testing by 2020.
format Online
Article
Text
id pubmed-9168140
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-91681402022-06-07 Biomarker Testing for Patients With Advanced/Metastatic Nonsquamous NSCLC in the United States of America, 2015 to 2021 Hess, Lisa M. Krein, Peter M. Haldane, Diane Han, Yimei Sireci, Anthony N. JTO Clin Res Rep Original Article INTRODUCTION: NSCLC is a solid tumor with a growing number of actionable biomarkers that may inform treatment. Current guidelines recommend a broad, panel-based approach be taken to identify actionable markers. This retrospective study used a deidentified electronic health records database in the United States to evaluate utilization of various testing modalities. METHODS: Data from all adult patients diagnosed with having advanced/metastatic nonsquamous NSCLC between January 2015 and March 2021 were eligible if there was evidence of systemic therapy within 90 days of diagnosis. RESULTS: Records from a total of 17,513 patients (91.6% from community-based practices) were eligible with 83,064 genomic biomarker tests recorded from 2015 to 2021. The proportion of patients who received biomarker testing by next-generation sequencing (NGS)-based methods ranged from 28.3% in 2015 to 68.1% in 2020. The proportion of biomarker testing methods with inconclusive or unsuccessful results ranged from 3.4% for NGS to 9.7% for fluorescence in situ hybridization. The median time to receive results ranged from 4.0 days for polymerase chain reaction-based tests to 10.0 days for immunohistochemistry- and NGS-based tests. Median time to receive results was 8 days for academic and 9 days for community practices. CONCLUSIONS: These real-world data suggest increased adoption of NGS-based testing, yet nearly one-third of all patients with advanced/metastatic nonsquamous NSCLC still did not receive broad-based genomic testing by 2020. Elsevier 2022-05-07 /pmc/articles/PMC9168140/ /pubmed/35677681 http://dx.doi.org/10.1016/j.jtocrr.2022.100336 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Hess, Lisa M.
Krein, Peter M.
Haldane, Diane
Han, Yimei
Sireci, Anthony N.
Biomarker Testing for Patients With Advanced/Metastatic Nonsquamous NSCLC in the United States of America, 2015 to 2021
title Biomarker Testing for Patients With Advanced/Metastatic Nonsquamous NSCLC in the United States of America, 2015 to 2021
title_full Biomarker Testing for Patients With Advanced/Metastatic Nonsquamous NSCLC in the United States of America, 2015 to 2021
title_fullStr Biomarker Testing for Patients With Advanced/Metastatic Nonsquamous NSCLC in the United States of America, 2015 to 2021
title_full_unstemmed Biomarker Testing for Patients With Advanced/Metastatic Nonsquamous NSCLC in the United States of America, 2015 to 2021
title_short Biomarker Testing for Patients With Advanced/Metastatic Nonsquamous NSCLC in the United States of America, 2015 to 2021
title_sort biomarker testing for patients with advanced/metastatic nonsquamous nsclc in the united states of america, 2015 to 2021
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168140/
https://www.ncbi.nlm.nih.gov/pubmed/35677681
http://dx.doi.org/10.1016/j.jtocrr.2022.100336
work_keys_str_mv AT hesslisam biomarkertestingforpatientswithadvancedmetastaticnonsquamousnsclcintheunitedstatesofamerica2015to2021
AT kreinpeterm biomarkertestingforpatientswithadvancedmetastaticnonsquamousnsclcintheunitedstatesofamerica2015to2021
AT haldanediane biomarkertestingforpatientswithadvancedmetastaticnonsquamousnsclcintheunitedstatesofamerica2015to2021
AT hanyimei biomarkertestingforpatientswithadvancedmetastaticnonsquamousnsclcintheunitedstatesofamerica2015to2021
AT sirecianthonyn biomarkertestingforpatientswithadvancedmetastaticnonsquamousnsclcintheunitedstatesofamerica2015to2021