Clinics and Practice (Aug 2022)

Accrual-Monitoring Practices for Various Disease Trials among AACI Member Cancer Centers

  • Zachary T. Elliott,
  • Zachary Goldberg,
  • Ramez Philips,
  • Jennifer M. Johnson,
  • Margaret T. Kasner,
  • William K. Kelly,
  • Sarah Osipowicz,
  • Rachael Dampman,
  • Joseph M. Curry

DOI
https://doi.org/10.3390/clinpract12050072
Journal volume & issue
Vol. 12, no. 5
pp. 692 – 700

Abstract

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Progress in the management of rare diseases, including rare cancers, is dependent upon clinical trials; however, as many as 32% of rare-disease trials go uncompleted or unpublished due to insufficient accrual. Monitoring practices may differ between institutions. We sought to survey the regulatory standards for various trial types among major U.S. cancer centers. A 10-question survey was designed using Qualtrics assessment software. The survey was sent via email to an internal server of member institutions of the Association of American Cancer Institutes (AACI). Of 103 AACI centers, 31% completed the survey (n = 32). Respondents differed in their definitions of a rare disease, minimum expectations for rare tumor studies, and frequency of accrual monitoring by their institutional Protocol Review and Monitoring Committee. Seventy-three percent of respondents did not close trials based on low accrual. Strategies to optimize accrual included investigator incentives for high accrual and penalties for low accrual in 37% and 13% of respondents, respectively.

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