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Genetic Counseling and Germline Testing in the Era of Tumor Sequencing: A Cohort Study

BACKGROUND: The clinical impact of addressing potential germline alterations from tumor-only next-generation sequencing (NGS) is not well characterized. Current guidelines for cancer genetic testing may miss clinically actionable germline changes, which may have important implications for cancer scr...

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Autores principales: Klek, Stefan, Heald, Brandie, Milinovich, Alex, Ni, Ying, Abraham, Jame, Mahdi, Haider, Estfan, Bassam, Khorana, Alok A, Bolwell, Brian J, Grivas, Petros, Sohal, Davendra P S, Funchain, Pauline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306190/
https://www.ncbi.nlm.nih.gov/pubmed/32596633
http://dx.doi.org/10.1093/jncics/pkaa018
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author Klek, Stefan
Heald, Brandie
Milinovich, Alex
Ni, Ying
Abraham, Jame
Mahdi, Haider
Estfan, Bassam
Khorana, Alok A
Bolwell, Brian J
Grivas, Petros
Sohal, Davendra P S
Funchain, Pauline
author_facet Klek, Stefan
Heald, Brandie
Milinovich, Alex
Ni, Ying
Abraham, Jame
Mahdi, Haider
Estfan, Bassam
Khorana, Alok A
Bolwell, Brian J
Grivas, Petros
Sohal, Davendra P S
Funchain, Pauline
author_sort Klek, Stefan
collection PubMed
description BACKGROUND: The clinical impact of addressing potential germline alterations from tumor-only next-generation sequencing (NGS) is not well characterized. Current guidelines for cancer genetic testing may miss clinically actionable germline changes, which may have important implications for cancer screening, treatment, and prevention. We examined whether increasing involvement of the clinical genetics service during somatic tumor-only NGS review at Molecular Tumor Board (MTB) increases the detection of germline findings. METHODS: In a retrospective evaluation of patients who underwent tumor-only NGS and were reviewed at MTB, we quantified genetic counseling (GC) referrals as well as germline testing uptake and results across three cohorts: before (C1) and after (C2) the addition of tumor-only NGS review and after (C3) instituting a formal process to coordinate NGS-based genetics referrals to preexisting oncology appointments. All statistical tests were two-sided. RESULTS: From 2013 to 2017, 907 tumor-only NGS reports were reviewed at MTB (n(C1) = 281, n(C2) = 493, n(C3) = 133); gastrointestinal (22.5%), lung (19.7%), genitourinary (14.8%), and breast (14.1%) were the most common index cancers. GC visits due to MTB increased with each successive cohort (C1 = 1.1%, C2 = 6.9%, C3 = 13.5%; P for trend [P(trend)] < .001), as did germline testing (C1 = 0.7%, C2 = 3.2%, C3 = 11.3%; P(trend) < .001). Diagnosis of germline pathogenic variants increased with each successive cohort (C1 = 1.4%, C2 = 2.0%, C3 = 7.5%; P(trend) = .003) and with germline pathogenic variants found by MTB review (C1 = 0.4%, C2 = 0.4%, C3 = 2.3%; P(trend) = .12). CONCLUSIONS: Both review of tumor-only NGS by genetics and the institution of a process coordinating GC with oncology appointments increased the discovery of germline pathogenic variants from tumor-only NGS testing. Furthermore, this process identified germline pathogenic variant carriers who would not have otherwise met standard criteria for germline testing.
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spelling pubmed-73061902020-06-25 Genetic Counseling and Germline Testing in the Era of Tumor Sequencing: A Cohort Study Klek, Stefan Heald, Brandie Milinovich, Alex Ni, Ying Abraham, Jame Mahdi, Haider Estfan, Bassam Khorana, Alok A Bolwell, Brian J Grivas, Petros Sohal, Davendra P S Funchain, Pauline JNCI Cancer Spectr Article BACKGROUND: The clinical impact of addressing potential germline alterations from tumor-only next-generation sequencing (NGS) is not well characterized. Current guidelines for cancer genetic testing may miss clinically actionable germline changes, which may have important implications for cancer screening, treatment, and prevention. We examined whether increasing involvement of the clinical genetics service during somatic tumor-only NGS review at Molecular Tumor Board (MTB) increases the detection of germline findings. METHODS: In a retrospective evaluation of patients who underwent tumor-only NGS and were reviewed at MTB, we quantified genetic counseling (GC) referrals as well as germline testing uptake and results across three cohorts: before (C1) and after (C2) the addition of tumor-only NGS review and after (C3) instituting a formal process to coordinate NGS-based genetics referrals to preexisting oncology appointments. All statistical tests were two-sided. RESULTS: From 2013 to 2017, 907 tumor-only NGS reports were reviewed at MTB (n(C1) = 281, n(C2) = 493, n(C3) = 133); gastrointestinal (22.5%), lung (19.7%), genitourinary (14.8%), and breast (14.1%) were the most common index cancers. GC visits due to MTB increased with each successive cohort (C1 = 1.1%, C2 = 6.9%, C3 = 13.5%; P for trend [P(trend)] < .001), as did germline testing (C1 = 0.7%, C2 = 3.2%, C3 = 11.3%; P(trend) < .001). Diagnosis of germline pathogenic variants increased with each successive cohort (C1 = 1.4%, C2 = 2.0%, C3 = 7.5%; P(trend) = .003) and with germline pathogenic variants found by MTB review (C1 = 0.4%, C2 = 0.4%, C3 = 2.3%; P(trend) = .12). CONCLUSIONS: Both review of tumor-only NGS by genetics and the institution of a process coordinating GC with oncology appointments increased the discovery of germline pathogenic variants from tumor-only NGS testing. Furthermore, this process identified germline pathogenic variant carriers who would not have otherwise met standard criteria for germline testing. Oxford University Press 2020-03-05 /pmc/articles/PMC7306190/ /pubmed/32596633 http://dx.doi.org/10.1093/jncics/pkaa018 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Klek, Stefan
Heald, Brandie
Milinovich, Alex
Ni, Ying
Abraham, Jame
Mahdi, Haider
Estfan, Bassam
Khorana, Alok A
Bolwell, Brian J
Grivas, Petros
Sohal, Davendra P S
Funchain, Pauline
Genetic Counseling and Germline Testing in the Era of Tumor Sequencing: A Cohort Study
title Genetic Counseling and Germline Testing in the Era of Tumor Sequencing: A Cohort Study
title_full Genetic Counseling and Germline Testing in the Era of Tumor Sequencing: A Cohort Study
title_fullStr Genetic Counseling and Germline Testing in the Era of Tumor Sequencing: A Cohort Study
title_full_unstemmed Genetic Counseling and Germline Testing in the Era of Tumor Sequencing: A Cohort Study
title_short Genetic Counseling and Germline Testing in the Era of Tumor Sequencing: A Cohort Study
title_sort genetic counseling and germline testing in the era of tumor sequencing: a cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306190/
https://www.ncbi.nlm.nih.gov/pubmed/32596633
http://dx.doi.org/10.1093/jncics/pkaa018
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