Cargando…

RAPID framework for improved access to precision oncology for lethal disease: Results from a modified multi-round delphi study

INTRODUCTION: Predictive oncology, germline technologies, and adaptive seamless trials are promising advances in the treatment of lethal cancers. Yet, access to these therapies is stymied by costly research, regulatory barriers, and structural inequalities worsened by the COVID-19 pandemic. METHODS:...

Descripción completa

Detalles Bibliográficos
Autores principales: Bright, Kristin, Mills, Anneliese, Bradford, John-Peter, Stewart, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012713/
https://www.ncbi.nlm.nih.gov/pubmed/36926496
http://dx.doi.org/10.3389/frhs.2023.1015621
_version_ 1784906660831035392
author Bright, Kristin
Mills, Anneliese
Bradford, John-Peter
Stewart, David J.
author_facet Bright, Kristin
Mills, Anneliese
Bradford, John-Peter
Stewart, David J.
author_sort Bright, Kristin
collection PubMed
description INTRODUCTION: Predictive oncology, germline technologies, and adaptive seamless trials are promising advances in the treatment of lethal cancers. Yet, access to these therapies is stymied by costly research, regulatory barriers, and structural inequalities worsened by the COVID-19 pandemic. METHODS: To address the need for a comprehensive strategy for rapid and more equitable access to breakthrough therapies for lethal cancers, we conducted a modified multi-round Delphi study with 70 experts in oncology, clinical trials, legal and regulatory processes, patient advocacy, ethics, drug development, and health policy in Canada, Europe, and the US. Semi-structured ethnographic interviews (n = 33) were used to identify issues and solutions that participants subsequently evaluated in a survey (n = 47). Survey and interview data were co-analyzed to refine topics for an in-person roundtable where recommendations for system change were deliberated and drafted by 26 participants. RESULTS: Participants emphasized major issues in patient access to novel therapeutics including burdens of time, cost, and transportation required to complete eligibility requirements or to participate in trials. Only 12% of respondents reported satisfaction with current research systems, with “patient access to trials” and “delays in study approval” the topmost concerns. CONCLUSION: Experts agree that an equity-centered precision oncology communication model should be developed to improve access to adaptive seamless trials, eligibility reforms, and just-in-time trial activation. International advocacy groups are a key mobilizer of patient trust and should be involved at every stage of research and therapy approval. Our results also show that governments can promote better and faster access to life-saving therapeutics by engaging researchers and payors in an ecosystem approach that responds to the unique clinical, structural, temporal, and risk-benefit situations that patients with life-threatening cancers confront.
format Online
Article
Text
id pubmed-10012713
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-100127132023-03-15 RAPID framework for improved access to precision oncology for lethal disease: Results from a modified multi-round delphi study Bright, Kristin Mills, Anneliese Bradford, John-Peter Stewart, David J. Front Health Serv Health Services INTRODUCTION: Predictive oncology, germline technologies, and adaptive seamless trials are promising advances in the treatment of lethal cancers. Yet, access to these therapies is stymied by costly research, regulatory barriers, and structural inequalities worsened by the COVID-19 pandemic. METHODS: To address the need for a comprehensive strategy for rapid and more equitable access to breakthrough therapies for lethal cancers, we conducted a modified multi-round Delphi study with 70 experts in oncology, clinical trials, legal and regulatory processes, patient advocacy, ethics, drug development, and health policy in Canada, Europe, and the US. Semi-structured ethnographic interviews (n = 33) were used to identify issues and solutions that participants subsequently evaluated in a survey (n = 47). Survey and interview data were co-analyzed to refine topics for an in-person roundtable where recommendations for system change were deliberated and drafted by 26 participants. RESULTS: Participants emphasized major issues in patient access to novel therapeutics including burdens of time, cost, and transportation required to complete eligibility requirements or to participate in trials. Only 12% of respondents reported satisfaction with current research systems, with “patient access to trials” and “delays in study approval” the topmost concerns. CONCLUSION: Experts agree that an equity-centered precision oncology communication model should be developed to improve access to adaptive seamless trials, eligibility reforms, and just-in-time trial activation. International advocacy groups are a key mobilizer of patient trust and should be involved at every stage of research and therapy approval. Our results also show that governments can promote better and faster access to life-saving therapeutics by engaging researchers and payors in an ecosystem approach that responds to the unique clinical, structural, temporal, and risk-benefit situations that patients with life-threatening cancers confront. Frontiers Media S.A. 2023-02-27 /pmc/articles/PMC10012713/ /pubmed/36926496 http://dx.doi.org/10.3389/frhs.2023.1015621 Text en © 2023 Bright, Mills, Bradford and Stewart. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Health Services
Bright, Kristin
Mills, Anneliese
Bradford, John-Peter
Stewart, David J.
RAPID framework for improved access to precision oncology for lethal disease: Results from a modified multi-round delphi study
title RAPID framework for improved access to precision oncology for lethal disease: Results from a modified multi-round delphi study
title_full RAPID framework for improved access to precision oncology for lethal disease: Results from a modified multi-round delphi study
title_fullStr RAPID framework for improved access to precision oncology for lethal disease: Results from a modified multi-round delphi study
title_full_unstemmed RAPID framework for improved access to precision oncology for lethal disease: Results from a modified multi-round delphi study
title_short RAPID framework for improved access to precision oncology for lethal disease: Results from a modified multi-round delphi study
title_sort rapid framework for improved access to precision oncology for lethal disease: results from a modified multi-round delphi study
topic Health Services
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012713/
https://www.ncbi.nlm.nih.gov/pubmed/36926496
http://dx.doi.org/10.3389/frhs.2023.1015621
work_keys_str_mv AT brightkristin rapidframeworkforimprovedaccesstoprecisiononcologyforlethaldiseaseresultsfromamodifiedmultirounddelphistudy
AT millsanneliese rapidframeworkforimprovedaccesstoprecisiononcologyforlethaldiseaseresultsfromamodifiedmultirounddelphistudy
AT bradfordjohnpeter rapidframeworkforimprovedaccesstoprecisiononcologyforlethaldiseaseresultsfromamodifiedmultirounddelphistudy
AT stewartdavidj rapidframeworkforimprovedaccesstoprecisiononcologyforlethaldiseaseresultsfromamodifiedmultirounddelphistudy