The impact of COVID-19 on cancer care and oncology clinical research: an experts' perspective.

Détails

Ressource 1Télécharger: 34953404_BIB_3E779B64CA41.pdf (460.82 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY-NC-ND 4.0
ID Serval
serval:BIB_3E779B64CA41
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
The impact of COVID-19 on cancer care and oncology clinical research: an experts' perspective.
Périodique
ESMO open
Auteur⸱e⸱s
Sessa C., Cortes J., Conte P., Cardoso F., Choueiri T., Dummer R., Lorusso P., Ottmann O., Ryll B., Mok T., Tempero M., Comis S., Oliva C., Peters S., Tabernero J.
ISSN
2059-7029 (Electronic)
ISSN-L
2059-7029
Statut éditorial
Publié
Date de publication
02/2022
Peer-reviewed
Oui
Volume
7
Numéro
1
Pages
100339
Langue
anglais
Notes
Publication types: Journal Article ; Review
Publication Status: ppublish
Résumé
The coronavirus disease-19 (COVID-19) pandemic promises to have lasting impacts on cancer clinical trials that could lead to faster patient access to new treatments. In this article, an international panel of oncology experts discusses the lasting impacts of the pandemic on oncology clinical trials and proposes solutions for clinical trial stakeholders, with the support of recent data on worldwide clinical trials collected by IQVIA. These lasting impacts and proposed solutions encompass three topic areas. Firstly, acceleration and implementation of new operational approaches to oncology trials with patient-centric, fully decentralized virtual approaches that include remote assessments via telemedicine and remote devices. Geographical differences in the uptake of remote technology, including telemedicine, are discussed in the article, focusing on the impact of the local adoption of new operational approaches. Secondly, innovative clinical trials. The pandemic has highlighted the need for new trial designs that accelerate research and limit risks and burden for patients while driving optimization of clinical trial objectives and endpoints, while testing is being minimized. Areas of considerations for clinical trial stakeholders are discussed in detail. In addition, the COVID-19 pandemic has exposed the underrepresentation of minority groups in clinical trials; the approach for oncology clinical trials to improve generalizability of efficacy and outcomes data is discussed. Thirdly, a new problem-focused collaborative framework between oncology trial stakeholders, including decision makers, to leverage and further accelerate the innovative approaches in clinical research developed during the COVID-19 pandemic. This could shorten timelines for patient access to new treatments by addressing the cultural and technological barriers to adopting new operational approaches and innovative clinical trials. The role of the different stakeholders is described, with the aim of making COVID-19 a catalyst for positive change in oncology clinical research and eventually in cancer care.
Mots-clé
COVID-19, Clinical Trials as Topic, Humans, Neoplasms/epidemiology, Neoplasms/therapy, Pandemics, SARS-CoV-2, Telemedicine, cancer care, clinical research, collaborative framework, real-world evidence
Pubmed
Web of science
Open Access
Oui
Création de la notice
04/01/2022 9:35
Dernière modification de la notice
25/01/2024 8:34
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