Evidence map›Paper›PMID 36480778›Full record

ReviewJCO precision oncology2022

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

Edwin Cuppen, Olivier Elemento, Richard Rosenquist, Svetlana Nikic, Maarten IJzerman, Isabelle Durand Zaleski, Geert Frederix, Lars-Åke Levin, Charles G Mullighan, Reinhard Buettner and 13 more

Open access · bronzeAbstract readReview
In one paragraph

Review in JCO precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
6.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 73 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 20 institutions in 11 countries.

Edwin CuppenHartwig Medical Foundation, Amsterdam, the Netherlands.ORCID 0000-0002-0400-9542
Olivier ElementoCaryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY.ORCID 0000-0002-8061-9617
Richard RosenquistDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-0211-8788
Svetlana NikicIllumina Productos de España, S.L.U., Plaza Pablo Ruiz Picasso, Madrid, Spain.
Maarten IJzermanErasmus School of Health Policy & Management, Erasmus University, Rotterdam, the Netherlands.
Isabelle Durand ZaleskiUniversité de Paris, CRESS, INSERM, INRA, URCEco, AP-HP, Hôpital de l'Hôtel Dieu, Paris, France.ORCID 0000-0002-4078-1476
Geert FrederixJulius Center for Health Sciences and Primary Care, University Medical Center, Utrecht, the Netherlands.
Lars-Åke LevinDepartment of Health, Medicine and Caring Sciences (HMV), Linköping University, Linköping, Sweden.ORCID 0000-0003-2581-4863
Charles G MullighanDepartment of Pathology, St Jude Children's Research Hospital, Memphis, TN.ORCID 0000-0002-1871-1850
Reinhard BuettnerInstitute of Pathology, University Hospital Cologne, Germany.ORCID 0000-0001-8806-4786
Trevor J PughDepartment of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-8073-5888
Sean GrimmondCentre for Cancer Research, University of Melbourne, Melbourne, Australia.ORCID 0000-0002-8102-7998
Carlos CaldasCancer Research UK Cambridge Institute and Department of Oncology, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0003-3547-1489
Fabrice AndreInstitut Gustave Roussy, Villejuif, France.ORCID 0000-0001-5795-8357
Ilse CustersStichting Lygature, Utrecht, the Netherlands.
Elias CampoInstitut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0001-9850-9793
Hans van SnellenbergHartwig Medical Foundation, Amsterdam, the Netherlands.
Anna SchuhUniversity of Oxford, Oxford, United Kingdom.ORCID 0000-0002-3938-8490
Hidewaki NakagawaLaboratory for Cancer Genomics, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan.ORCID 0000-0003-1807-772X
Christof von KalleBerlin Institute of Health at Charité-Universitätsmedizin Berlin, Clinical Study Center, Berlin, Germany.
Torsten HaferlachMunich Leukemia Laboratory, Munich, Germany.
Stefan FröhlingDivision of Translational Medical Oncology, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.ORCID 0000-0001-7907-4595
Vaidehi JobanputraNew York Genome Center; Department of Pathology, Columbia University Irving Medical Center, New York, NY.ORCID 0000-0003-0962-7873
The University of Melbourne · AUUniversity Medical Center Utrecht · NLBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DECornell University · USGerman Cancer Research Center · DEHartwig Medical Foundation · NLHospital Clínic de Barcelona · ESInserm · FRInstitut Gustave Roussy · FRKarolinska University Hospital · SELinköping University · SELygature · NLMunich Leukemia Laboratory (Germany) · DENew York Genome Center · USOntario Institute for Cancer Research · CARIKEN Center for Integrative Medical Sciences · JPSt. Jude Children's Research Hospital · USUniversity Hospital Cologne · DEUniversity of Cambridge · GBUniversity of Oxford · GB

Funding

Translating genomic discoveries to improved outcomes for high risk acute leukemiaR35CA197695 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Charles G Mullighan · 2017 to 2026
$11.4M
Cancer Research UK 16942Cancer Research UK 29567Cancer Research UK A17197Cancer Research UK A27657Cancer Research UK A29580Medical Research Council MR/P012442/1NCI NIH HHS R35 CA197695
6 · The paper itself

Abstract

purposeThe 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.

methodsHere, 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.

resultsWe 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.

conclusionWGTS 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.

Indexed as

NeoplasmsHumans

Identifiers

PMID36480778
PMCPMC10166391
OpenAlexW4310887545

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.