Publication

Creating and Implementing a Principal Investigator Tool Kit for Enhancing Accrual to Late Phase Clinical Trials: Development and Usability Study

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Last modified
  • 06/25/2025
Type of Material
Authors
    Kristin Higgins, Emory UniversityAlexandra Thomas, Wake Forest Baptist Medical CenterNancy Soto, American College of Radiology, RestonRebecca Paulus, American College of Radiology, RestonThomas J George, University of Florida College of MedicineThomas B Julian, Allegheny General HospitalSharon Hartson Stine, American College of Radiology, RestonMerry Jennifer Markham, University of Florida College of MedicineMaria Werner-Wasik, Sidney Kimmel Cancer Center at Jefferson
Language
  • English
Date
  • 2022-07-01
Publisher
  • JMIR Cancer
Publication Version
Copyright Statement
  • ©Kristin A Higgins, Alexandra Thomas, Nancy Soto, Rebecca Paulus, Thomas J George, Thomas B Julian, Sharon Hartson Stine, Merry Jennifer Markham, Maria Werner-Wasik. Originally published in JMIR Cancer (https://cancer.jmir.org), 25.08.2022.
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 8
Issue
  • 3
Start Page
  • e38514
End Page
  • e38514
Grant/Funding Information
  • This project was supported by grants U10CA180868 (NRG Oncology Operations) from the National Cancer Institute (NCI).
Supplemental Material (URL)
Abstract
  • Background: Accrual to oncology clinical trials remains a challenge, particularly during the COVID-19 pandemic. For late phase clinical trials funded by the National Cancer Institute, the development of these research protocols is a resource-intensive process; however, mechanisms to optimize patient accrual after trial activation are underdeveloped across the National Clinical Trial Network (NCTN). Low patient accrual can lead to the premature closure of clinical trials and can ultimately delay the availability of new, potentially life-saving therapies in oncology. Objective: The purpose of this study is to formally create an easily implemented tool kit of resources for investigators of oncology clinical trials within the NCTN, specifically the NRG Oncology cooperative group, in order to optimize patient accrual. Methods: NRG Oncology sought to formally develop a tool kit of resources to use at specific time points during the lifetime of NRG Oncology clinical trials. The tools are clearly described and involve the facilitation of engagement of the study principal investigator with the scientific and patient advocate community during the planning, activation, and accrual periods. Social media tools are also leveraged to enhance such engagement. The principal investigator (PI) tool kit was created in 2019 and thereafter piloted with the NRG Oncology/Alliance NRG-LU005 phase II or III trial in small-cell lung cancer. The PI tool kit was developed by the NRG Oncology Protocol Operations Management committee and was tested with the NRG/Alliance LU005 randomized trial within the NCTN. Results: NRG Oncology/Alliance NRG-LU005 has seen robust enrollment, currently 127% of the projected accrual. Importantly, many of the tool kit elements are already being used in ongoing NRG Oncology trials, with 56% of active NRG trials using at least one element of the PI tool kit and all in-development trials offered the resource. This underscores the feasibility and potential benefits of deploying the PI tool kit across all NRG Oncology trials moving forward. Conclusions: While clinical trial accrual can be challenging, the PI tool kit has been shown to augment accrual in a low-cost and easily implementable fashion. It could be widely and consistently deployed across the NCTN to improve accrual in oncology clinical trials.
Author Notes
  • Kristin A Higgins, Winship Cancer Institute, Emory University, 1365 C Clifton Road Northeast, Atlanta, GA, 30322, United States, Phone: 1 (404) 778 0603, Email: kristin.higgins@emory.edu
Keywords
Research Categories
  • Health Sciences, Oncology

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