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Identifying the steps required to effectively implement next-generation sequencing in oncology at a national level in Europe
ID Horgan, Denis (Author), ID Čufer, Tanja (Author), et al.

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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.

Language:English
Keywords:clinical standardization, equitable reimbursement, European Alliance for Personalised Medicine, Europe’s Beating Cancer Plan, evidence generation, governance, molecularly guided treatment options, next-generation sequencing, stakeholder awareness and education, testing infrastructure
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:MF - Faculty of Medicine
Publication status:Published
Publication version:Version of Record
Year:2022
Number of pages:27 str.
Numbering:Vol. 12, iss. 1, art. 72
PID:20.500.12556/RUL-137400 This link opens in a new window
ISSN on article:2075-4426
DOI:10.3390/jpm12010072 This link opens in a new window
COBISS.SI-ID:140518403 This link opens in a new window
Publication date in RUL:16.06.2022
Views:600
Downloads:129
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Record is a part of a journal

Title:Journal of personalized medicine
Shortened title:J. pers. med.
Publisher:MDPI
ISSN:2075-4426
COBISS.SI-ID:31207641 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:klinična standardizacija, pravično povračilo, Evropska zveza za personalizirano medicino, Evropski načrt za premagovanje raka, pridobivanje dokazov, upravljanje, molekularno vodene možnosti zdravljenja, sekvenciranje naslednje generacije, ozaveščanje in izobraževanje deležnikov, testiranje infrastrukture

Projects

Funder:Other - Other funder or multiple funders
Funding programme:Novartis

Funder:Other - Other funder or multiple funders
Funding programme:AstraZeneca

Funder:Other - Other funder or multiple funders
Funding programme:F. Hoffmann-La Roche Ltd.

Funder:Other - Other funder or multiple funders
Funding programme:Exact Sciences

Funder:Other - Other funder or multiple funders
Funding programme:Eli Lilly and Company

Funder:Other - Other funder or multiple funders
Funding programme:Illumina

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