Abstract

AimThough patient engagement in clinical research is growing, recent reports suggest few clinical trials report on such activities. To address this gap, we describe our approach to patient engagement in the development of a clinical trial protocol to assess a new immunotherapy for blood cancer (chimeric antigen receptor T-cell therapy, CAR-T cell therapy).MethodsOur team developed a clinical trial protocol by working with patient partners from inception. Two patient partners with lived blood cancer experience were identified through referrals from our team’s professional network and patient organization contacts. Our patient partners were onboarded to the team and engaged in several studies conducted to develop the clinical trial protocol, including a systematic review of the existing literature on the therapy, patient interviews and a survey to obtain perspectives on barriers and enablers to participating in the trial, an early economic analysis, and a retrospective cohort study.ResultsEngaging patient partners enhanced our research in ways that would not have otherwise occurred. By selecting patient important outcomes for data collection, our partners helped flag that quality of life and health utility measures have not been reported in previous CAR-T cell therapy trials for blood cancer. Our partners also co-developed a non-technical summary of the systematic review that summarized results in an accessible manner. Our patient partners reviewed interview and survey questions, to improve the language and appropriateness; provided recruitment suggestions; and provided a patient perspective on the results, thereby confirming the importance of findings. Input was also obtained on costs for the early economic analysis. Our patient partners identified costs that may be a burden to both patients and caregivers during a trial and helped to confirm that the overall structure of the economic model reflected the patient care pathway. Our patient partners also shared their diagnosis and treatment stories, which helped to provide the research team with insight into this experience.ConclusionsContributions by our patient partners were invaluable to each component study, as well as the overall development of the trial protocol. We plan to use this approach in the future in order to meaningfully engage patients in the development of other clinical trials; we also hope that by reporting our methods this will help other research teams to do the same.Trial registrationAffiliated with the development of NCT03765177.

Highlights

  • Patient engagement, the involvement of patients, caregivers, friends and family members in the research process, has numerous proposed benefits [1,2,3,4,5]

  • By selecting patient important outcomes for data collection, our partners helped flag that quality of life and health utility measures have not been reported in previous Chimeric antigen receptor T-cell therapy (CAR-T) cell therapy trials for blood cancer

  • We found that of the 60 clinical trials identified by our systematic review, none reported these outcome measures [15]

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Summary

Introduction

The involvement of patients, caregivers, friends and family members in the research process, has numerous proposed benefits [1,2,3,4,5]. It’s suggested that patient and caregiver partners may help to ensure research findings are communicated in an appropriate manner and improve dissemination of results in traditional and novel channels [5]. In addition to these benefits, it has been argued that an ethical obligation underlies the need to involve patients as they are the “ultimate end-users” of the knowledge generated, and in the case of publicly funded research, patients may want to ensure resources are allocated to areas felt to be of priority [5, 13]

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