Evidence map›Paper›PMID 35055387›Full record

ArticleJournal of personalized medicine2022

Identifying the Steps Required to Effectively Implement Next-Generation Sequencing in Oncology at a National Level in Europe.

Denis Horgan, Giuseppe Curigliano, Olaf Rieß, Paul Hofman, Reinhard Büttner, Pierfranco Conte, Tanja Cufer, William M Gallagher, Nadia Georges, Keith Kerr and 10 more

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
–field-weighted citation impact
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

36 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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

20 authors.

Denis HorganEuropean Alliance for Personalised Medicine, Avenue de l'Armee/Legerlaan 10, 1040 Brussels, Belgium.
Giuseppe CuriglianoEuropean Institute of Oncology, IRCCS, Via Giuseppe Ripamonti, 435, 20141 Milan, Italy.ORCID 0000-0003-1781-2518
Olaf RießInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Calwerstrasse 7, 72070 Tuebingen, Germany.
Paul HofmanLaboratory of Clinical and Experimental Pathology, University of Côte d'Azur, FHU OncoAge, Biobank BB-0033-00025, Pasteur Hospital, 30 Avenue de la voie Romaine, CEDEX 01, 06001 Nice, France.ORCID 0000-0003-0431-9353
Reinhard BüttnerInstitute for Pathology, University Hospital Cologne, Kerpener Str. 62, 50937 Cologne, Germany.ORCID 0000-0001-8806-4786
Pierfranco ConteThe Veneto Institute of Oncology, IRCCS, Via Gattamelata, 64, 35128 Padua, Italy.
Tanja CuferMedical Faculty, University of Ljubljana, Vrazov trg 2, 1000 Ljubljana, Slovenia.
William M GallagherSchool of Biomolecular and Biomedical Science, University College Dublin, Belfield, D04 V1W8 Dublin, Ireland.ORCID 0000-0002-4307-5999
Nadia GeorgesExact Sciences, Quai du Seujet 10, 1201 Geneva, Switzerland.
Keith KerrSchool of Medicine and Dentistry, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK.
Frédérique Penault-LlorcaCentre Jean Perrin, 58, Rue Montalembert, CEDEX 01, 63011 Clermont-Ferrand, France.
Ken MastrisEuropa Uomo, Leopoldstraat 34, 2000 Antwerp, Belgium.ORCID 0000-0002-6074-8147
Carla PintoAstraZeneca, Rua Humberto Madeira 7, 1800 Oeiras, Portugal.
Jan Van MeerbeeckAntwerp University Hospital, University of Antwerp, Wijlrijkstraat 10, 2650 Edegem, Belgium.
Elisabetta MunzoneEuropean Institute of Oncology, IRCCS, Via Giuseppe Ripamonti, 435, 20141 Milan, Italy.ORCID 0000-0003-3371-3878
Marlene ThomasF. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, 4070 Basel, Switzerland.
Sonia UjupanEli Lilly and Company, Rue du Marquis 1, Markiesstraat, 1000 Brussels, Belgium.
Gilad W VainerDepartment of Pathology, Hadassah Hebrew-University Medical Center, Hebrew University of Jerusalem, Kalman Ya'akov Man St, Jerusalem 91905, Israel.ORCID 0000-0002-8828-8138
Janna-Lisa VelthausUniversity Medical Center Hamburg-Eppendorf, Martinistraße 52, 20251 Hamburg, Germany.
Fabrice AndréInstitut Gustave Roussy, 114 Rue Edouard Vaillant, 94805 Villejuif, France.

Funding

Astrazeneca N/AEli Lilly N/AExact Sciences N/AF. Hoffman-La Roche N/AIllumina N/ANovartis N/A
6 · The paper itself

Abstract

Next-generation sequencing (NGS) may enable more focused and highly personalized cancer treatment, with the National Comprehensive Cancer Network and European Society for Medical Oncology guidelines now recommending NGS for daily clinical practice for several tumor types. However, NGS implementation, and therefore patient access, varies across Europe; a multi-stakeholder collaboration is needed to establish the conditions required to improve this discrepancy. In that regard, we set up European Alliance for Personalised Medicine (EAPM)-led expert panels during the first half of 2021, including key stakeholders from across 10 European countries covering medical, economic, patient, industry, and governmental expertise. We describe the outcomes of these panels in order to define and explore the necessary conditions for NGS implementation into routine clinical care to enable patient access, identify specific challenges in achieving them, and make short- and long-term recommendations. The main challenges identified relate to the demand for NGS tests (governance, clinical standardization, and awareness and education) and supply of tests (equitable reimbursement, infrastructure for conducting and validating tests, and testing access driven by evidence generation). Recommendations made to resolve each of these challenges should aid multi-stakeholder collaboration between national and European initiatives, to complement, support, and mutually reinforce efforts to improve patient care.

Indexed as

clinical standardizationequitable reimbursementEuropean Alliance for Personalised MedicineEurope’s Beating Cancer Planevidence generationgovernancemolecularly guided treatment optionsnext-generation sequencingstakeholder awareness and educationtesting infrastructure

Identifiers

PMID35055387
PMCPMC8780351

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.