TY - JOUR
T1 - Identifying the Steps Required to Effectively Implement Next-Generation Sequencing in Oncology at a National Level in Europe
AU - Horgan, Denis
AU - Curigliano, Giuseppe
AU - Rieß, Olaf
AU - Hofman, Paul
AU - Büttner, Reinhard
AU - Conte, Pierfranco
AU - Cufer, Tanja
AU - Gallagher, William M.
AU - Georges, Nadia
AU - Kerr, Keith
AU - Penault-Llorca, Frédérique
AU - Mastris, Ken
AU - Pinto, Carla
AU - Meerbeeck, Jan Van
AU - Munzone, Elisabetta
AU - Thomas, Marlene
AU - Ujupan, Sonia
AU - Vainer, Gilad W.
AU - Velthaus, Janna Lisa
AU - André, Fabrice
N1 - Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - 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.
AB - 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.
KW - Clinical standardization
KW - Equitable reimbursement
KW - European Alliance for Personalised Medicine
KW - Europe’s Beating Cancer Plan
KW - Evidence generation
KW - Governance
KW - Molecularly guided treatment options
KW - Next-generation sequencing
KW - Stakeholder awareness and education
KW - Testing infrastructure
UR - http://www.scopus.com/inward/record.url?scp=85122688796&partnerID=8YFLogxK
U2 - 10.3390/jpm12010072
DO - 10.3390/jpm12010072
M3 - Article
AN - SCOPUS:85122688796
SN - 2075-4426
VL - 12
JO - Journal of Personalized Medicine
JF - Journal of Personalized Medicine
IS - 1
M1 - 72
ER -