Abstract
Background
Novel therapies often fail to reach the bedside due to low trial recruitment rates. Prior to conducting one of the first chimeric antigen receptor (CAR) T cell therapy trials in Canada, we used the Theoretical Domains Framework, a novel tool for identifying barriers and enablers to behavior change, to identify physician-related barriers and enablers to screening and recruiting patients for an early phase immunotherapy trial.
Methods
We conducted interviews with hematologists across Canada and used a directed content analysis to identify relevant domains reflecting the key factors that may affect screening and recruitment.
Results
In total, we interviewed 15 hematologists. Physicians expressed “cautious hope”; while expressing safety, feasibility, and screening criteria concerns, 14 out of 15 hematologists intended to screen for the trial (domains: knowledge, goals, beliefs about consequences, intentions). Physicians underscored the “challenging contexts,” identifying resources, workload, forgetting, and patient wait times to receive CAR T cells as key practical barriers to screening (domains: environmental context and resources, memory, attention and decision-making, behavioral regulation). They also highlighted “variability in roles and procedures” that may lead to missed trial candidates (domain: social and professional role). Left unaddressed, these barriers may undermine trial recruitment.
Conclusions
This study is among the first to use the Theoretical Domains Framework from the physician perspective to identify recruitment challenges to early phase trials and demonstrates the value of this approach for identifying barriers to screening and recruitment that may not otherwise have been elicited. This approach can optimize trial procedures and may serve to inform future promising early phase cancer therapy trials.
Trial registration
ClinicalTrials.gov Identifier: NCT03765177. Registered on December 5, 2018.
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Details
1 Ottawa Hospital Research Institute, Clinical Epidemiology Program, Ottawa, Canada (GRID:grid.412687.e) (ISNI:0000 0000 9606 5108); Ottawa Hospital Research Institute, Blueprint Translational Research Group, Ottawa, Canada (GRID:grid.412687.e) (ISNI:0000 0000 9606 5108)
2 Ottawa Hospital Research Institute, Clinical Epidemiology Program, Ottawa, Canada (GRID:grid.412687.e) (ISNI:0000 0000 9606 5108); Ottawa Hospital Research Institute, Blueprint Translational Research Group, Ottawa, Canada (GRID:grid.412687.e) (ISNI:0000 0000 9606 5108); University of Ottawa at the Ottawa Hospital General Campus, Department of Anaesthesiology and Pain Medicine, Ottawa, Canada (GRID:grid.28046.38) (ISNI:0000 0001 2182 2255)
3 Ottawa Hospital Research Institute, Clinical Epidemiology Program, Ottawa, Canada (GRID:grid.412687.e) (ISNI:0000 0000 9606 5108); The Ottawa Hospital, Blood and Marrow Transplant Program, Ottawa, Canada (GRID:grid.412687.e) (ISNI:0000 0000 9606 5108)
4 Ottawa Hospital Research Institute, Clinical Epidemiology Program, Ottawa, Canada (GRID:grid.412687.e) (ISNI:0000 0000 9606 5108); Ottawa Hospital Research Institute, Blueprint Translational Research Group, Ottawa, Canada (GRID:grid.412687.e) (ISNI:0000 0000 9606 5108); University of Ottawa, School of Epidemiology and Public Health, Ottawa, Canada (GRID:grid.28046.38) (ISNI:0000 0001 2182 2255)
5 Patient Partners, Ottawa, Canada (GRID:grid.28046.38)
6 Ottawa Hospital Research Institute, Clinical Epidemiology Program, Ottawa, Canada (GRID:grid.412687.e) (ISNI:0000 0000 9606 5108); University of Ottawa, School of Epidemiology and Public Health, Ottawa, Canada (GRID:grid.28046.38) (ISNI:0000 0001 2182 2255); University of Ottawa, Institute for Clinical and Evaluative Sciences (ICES), Ottawa, Canada (GRID:grid.28046.38) (ISNI:0000 0001 2182 2255)
7 Patient Partners, Ottawa, Canada (GRID:grid.412687.e)
8 BC Cancer Genome Sciences Centre, Vancouver, Canada (GRID:grid.434706.2) (ISNI:0000 0004 0410 5424)
9 Vancouver General Hospital, Leukemia/BMT Program, Vancouver, Canada (GRID:grid.412541.7) (ISNI:0000 0001 0684 7796)




