TY - JOUR
T1 - Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care
AU - Cuppen, Edwin
AU - Elemento, Olivier
AU - Rosenquist, Richard
AU - Nikic, Svetlana
AU - IJzerman, Maarten
AU - Zaleski, Isabelle Durand
AU - Frederix, Geert
AU - Levin, Lars Åke
AU - Mullighan, Charles G.
AU - Buettner, Reinhard
AU - Pugh, Trevor J.
AU - Grimmond, Sean
AU - Caldas, Carlos
AU - Andre, Fabrice
AU - Custers, Ilse
AU - Campo, Elias
AU - van Snellenberg, Hans
AU - Schuh, Anna
AU - Nakagawa, Hidewaki
AU - von Kalle, Christof
AU - Haferlach, Torsten
AU - Fröhling, Stefan
AU - Jobanputra, Vaidehi
N1 - Publisher Copyright:
© 2022 by American Society of Clinical Oncology.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - PURPOSE 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.
AB - PURPOSE 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.
UR - http://www.scopus.com/inward/record.url?scp=105000560163&partnerID=8YFLogxK
U2 - 10.1200/PO.22.00245
DO - 10.1200/PO.22.00245
M3 - Article
C2 - 36480778
AN - SCOPUS:105000560163
SN - 2473-4284
VL - 6
JO - JCO Precision Oncology
JF - JCO Precision Oncology
M1 - e2200245
ER -