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Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care

The combination of whole-genome and transcriptome sequencing (WGTS) is expected to transform diagnosis and treatment for patients with cancer. WGTS is a comprehensive precision diagnostic test that is starting to replace the standard of care for oncology molecular testing in health care systems arou...

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Autores principales: Cuppen, Edwin, Elemento, Olivier, Rosenquist, Richard, Nikic, Svetlana, IJzerman, Maarten, Zaleski, Isabelle Durand, Frederix, Geert, Levin, Lars-Åke, Mullighan, Charles G., Buettner, Reinhard, Pugh, Trevor J., Grimmond, Sean, Caldas, Carlos, Andre, Fabrice, Custers, Ilse, Campo, Elias, van Snellenberg, Hans, Schuh, Anna, Nakagawa, Hidewaki, von Kalle, Christof, Haferlach, Torsten, Fröhling, Stefan, Jobanputra, Vaidehi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166391/
https://www.ncbi.nlm.nih.gov/pubmed/36480778
http://dx.doi.org/10.1200/PO.22.00245
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author Cuppen, Edwin
Elemento, Olivier
Rosenquist, Richard
Nikic, Svetlana
IJzerman, Maarten
Zaleski, Isabelle Durand
Frederix, Geert
Levin, Lars-Åke
Mullighan, Charles G.
Buettner, Reinhard
Pugh, Trevor J.
Grimmond, Sean
Caldas, Carlos
Andre, Fabrice
Custers, Ilse
Campo, Elias
van Snellenberg, Hans
Schuh, Anna
Nakagawa, Hidewaki
von Kalle, Christof
Haferlach, Torsten
Fröhling, Stefan
Jobanputra, Vaidehi
author_facet Cuppen, Edwin
Elemento, Olivier
Rosenquist, Richard
Nikic, Svetlana
IJzerman, Maarten
Zaleski, Isabelle Durand
Frederix, Geert
Levin, Lars-Åke
Mullighan, Charles G.
Buettner, Reinhard
Pugh, Trevor J.
Grimmond, Sean
Caldas, Carlos
Andre, Fabrice
Custers, Ilse
Campo, Elias
van Snellenberg, Hans
Schuh, Anna
Nakagawa, Hidewaki
von Kalle, Christof
Haferlach, Torsten
Fröhling, Stefan
Jobanputra, Vaidehi
author_sort Cuppen, Edwin
collection PubMed
description The combination of whole-genome and transcriptome sequencing (WGTS) is expected to transform diagnosis and treatment for patients with cancer. WGTS is a comprehensive precision diagnostic test that is starting to replace the standard of care for oncology molecular testing in health care systems around the world; however, the implementation and widescale adoption of this best-in-class testing is lacking. METHODS: Here, we address the barriers in integrating WGTS for cancer diagnostics and treatment selection and answer questions regarding utility in different cancer types, cost-effectiveness and affordability, and other practical considerations for WGTS implementation. RESULTS: We review the current studies implementing WGTS in health care systems and provide a synopsis of the clinical evidence and insights into practical considerations for WGTS implementation. We reflect on regulatory, costs, reimbursement, and incidental findings aspects of this test. CONCLUSION: WGTS is an appropriate comprehensive clinical test for many tumor types and can replace multiple, cascade testing approaches currently performed. Decreasing sequencing cost, increasing number of clinically relevant aberrations and discovery of more complex biomarkers of treatment response, should pave the way for health care systems and laboratories in implementing WGTS into clinical practice, to transform diagnosis and treatment for patients with cancer.
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spelling pubmed-101663912023-05-09 Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care Cuppen, Edwin Elemento, Olivier Rosenquist, Richard Nikic, Svetlana IJzerman, Maarten Zaleski, Isabelle Durand Frederix, Geert Levin, Lars-Åke Mullighan, Charles G. Buettner, Reinhard Pugh, Trevor J. Grimmond, Sean Caldas, Carlos Andre, Fabrice Custers, Ilse Campo, Elias van Snellenberg, Hans Schuh, Anna Nakagawa, Hidewaki von Kalle, Christof Haferlach, Torsten Fröhling, Stefan Jobanputra, Vaidehi JCO Precis Oncol Special Articles The combination of whole-genome and transcriptome sequencing (WGTS) is expected to transform diagnosis and treatment for patients with cancer. WGTS is a comprehensive precision diagnostic test that is starting to replace the standard of care for oncology molecular testing in health care systems around the world; however, the implementation and widescale adoption of this best-in-class testing is lacking. METHODS: Here, we address the barriers in integrating WGTS for cancer diagnostics and treatment selection and answer questions regarding utility in different cancer types, cost-effectiveness and affordability, and other practical considerations for WGTS implementation. RESULTS: We review the current studies implementing WGTS in health care systems and provide a synopsis of the clinical evidence and insights into practical considerations for WGTS implementation. We reflect on regulatory, costs, reimbursement, and incidental findings aspects of this test. CONCLUSION: WGTS is an appropriate comprehensive clinical test for many tumor types and can replace multiple, cascade testing approaches currently performed. Decreasing sequencing cost, increasing number of clinically relevant aberrations and discovery of more complex biomarkers of treatment response, should pave the way for health care systems and laboratories in implementing WGTS into clinical practice, to transform diagnosis and treatment for patients with cancer. Wolters Kluwer Health 2022-12-08 /pmc/articles/PMC10166391/ /pubmed/36480778 http://dx.doi.org/10.1200/PO.22.00245 Text en © 2022 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Special Articles
Cuppen, Edwin
Elemento, Olivier
Rosenquist, Richard
Nikic, Svetlana
IJzerman, Maarten
Zaleski, Isabelle Durand
Frederix, Geert
Levin, Lars-Åke
Mullighan, Charles G.
Buettner, Reinhard
Pugh, Trevor J.
Grimmond, Sean
Caldas, Carlos
Andre, Fabrice
Custers, Ilse
Campo, Elias
van Snellenberg, Hans
Schuh, Anna
Nakagawa, Hidewaki
von Kalle, Christof
Haferlach, Torsten
Fröhling, Stefan
Jobanputra, Vaidehi
Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care
title Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care
title_full Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care
title_fullStr Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care
title_full_unstemmed Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care
title_short Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care
title_sort implementation of whole-genome and transcriptome sequencing into clinical cancer care
topic Special Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166391/
https://www.ncbi.nlm.nih.gov/pubmed/36480778
http://dx.doi.org/10.1200/PO.22.00245
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