Impact of Workforce Challenges and Funds Flow on Cancer Clinical Trial Development and Conduct

Author:

Pennell Nathan A.1,Szczepanek Connie2,Spigel David3,Ramalingam Suresh S.4

Affiliation:

1. Cleveland Clinic Taussig Cancer Institute, Cleveland, OH

2. Cancer Research Consortium of West Michigan, Grand Rapids, MI

3. Sarah Cannon Research Institute, Nashville, TN

4. Winship Cancer Institute of Emory University, Atlanta, GA

Abstract

The conduct of clinical cancer research has faced considerable challenges in recent years, and the situation has only been exacerbated by the global pandemic. The growing complexity of clinical trials and rising administrative burdens had been causing greater expense and difficulty in recruiting and retaining an appropriately trained workforce even before the well-publicized increase in turnover caused by the pandemic. Longstanding issues such as restrictive inclusion criteria and complicated trial designs have negatively affected already low clinical trial accrual rates, limited sites capable of opening studies and enrolling patients, and worsened disparities in trial participation. Opposing these elements are efforts by ASCO and other organizations to increase affordability, access, and equity in clinical trial enrollment. To provide diverse perspectives on how these challenges are affecting cancer research as we emerge from the pandemic, we asked a panel of experienced clinical research leaders from both academic and community cancer centers to answer questions they felt most pressing about the business of conducting clinical research today and where they felt the field was moving in the near future.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

General Medicine

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