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

被引:26
|
作者
Sessa, C. [1 ]
Cortes, J. [2 ]
Conte, P. [3 ]
Cardoso, F. [4 ]
Choueiri, T. [5 ]
Dummer, R. [6 ]
Lorusso, P. [7 ]
Ottmann, O. [8 ]
Ryll, B. [9 ]
Mok, T. [10 ]
Tempero, M. [11 ]
Comis, S. [12 ]
Oliva, C. [13 ]
Peters, S. [14 ]
Tabernero, J. [15 ]
机构
[1] Osped San Giovanni Bellinzona, Oncol Inst Southern Switzerland, Via A Gallino 12, CH-6500 Bellinzona, Switzerland
[2] Georgia Canc Ctr, Augusta, GA USA
[3] Univ Padua, Padua, Italy
[4] Champalimaud Canc Ctr, Lisbon, Portugal
[5] Dana Farber Canc Inst, Boston, MA 02115 USA
[6] Univ Hosp Zurich, Zurich, Switzerland
[7] Yale Univ, Yale Canc Ctr, New Haven, CT USA
[8] Cardiff Univ, Cardiff, Wales
[9] Melanoma Patient Network Europe, Uppsala, Sweden
[10] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Clin Oncol, Shatin, Hong Kong, Peoples R China
[11] Univ Calif San Francisco, Pancreas Ctr, San Francisco, CA 94143 USA
[12] IQVIA, Milan, Italy
[13] IQVIA, Reading, Berks, England
[14] Ctr Oncol CHUV, Lausanne, Switzerland
[15] Vall dHebron Inst Oncol, Barcelona, Spain
关键词
cancer care; clinical research; real-world evidence; collaborative framework; COVID-19;
D O I
10.1016/j.esmoop.2021.100339
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
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页数:8
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