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. 2020 Jul 1;26(13):3100-3103.
doi: 10.1158/1078-0432.CCR-20-1364. Epub 2020 Apr 20.

Adapting to a Pandemic - Conducting Oncology Trials during the SARS-CoV-2 Pandemic

Affiliations

Adapting to a Pandemic - Conducting Oncology Trials during the SARS-CoV-2 Pandemic

Aaron C Tan et al. Clin Cancer Res. .

Abstract

The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) pandemic has necessitated changes in cancer care delivery as resources are reallocated. Clinical trials and other research activities are inevitably impacted. Start-up activities for new trials may be deferred and recruitment suspended. For patients already enrolled however, there are challenges in continuing treatment on trial. Regulatory bodies have issued guidance on managing clinical trials during the pandemic, including contingency measures for remote study visits, delivery of investigational product, and site monitoring visits. New cancer clinical trial practices during the SARS-CoV-2 pandemic include new risk assessment strategies, decentralized and remote trial coordination, data collection, and delegation of specific therapeutic activities. This experience could provide evidence of more feasible and cost-effective methods for future clinical trial conduct.

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Conflict of interest statement

D.M. Ashley is an employee/paid consultant for Istari Oncology, Oblato, and Diverse Biopharma, and holds ownership interest (including patents) in Istari. M. Khasraw reports receiving other commercial research support from Bristol-Myers Squibb and AbbVie. No potential conflicts of interest were disclosed by the other author.

Figures

Figure 1.
Figure 1.
Decentralized versus traditional clinical trial models. Adapted from Khozin and colleagues (21).
Figure 2.
Figure 2.
Primary and satellite clinical trial sites. Adapted from Sabesan and colleagues (17).

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