Evaluating the impact of delayed study startup on accrual in cancer studies
Isuru Ratnayake, Anh-Tuan Do, Daniel Gajewski, Sam Pepper, Oluwatobiloba Ige, Natalie Streeter, Tara L. Lin, Matthew McGuirk, Byron Gajewski, Dinesh Pal Mudaranthakam

TL;DR
This paper examines how delays in starting cancer clinical trials affect their success, finding that shorter startup times are linked to better outcomes.
Contribution
The study quantifies the relationship between delayed study startup and accrual success in cancer trials using real-world data.
Findings
Studies meeting 70% accrual have a median activation time of 140.5 days, while those failing have 187 days.
Late-phase studies take longer to activate than early-phase ones (p-value=0.001).
Shorter activation times correlate with higher study success across all accrual thresholds.
Abstract
Drug development in cancer medicine depends on high-quality clinical trials, but these require large investments of time to design, operationalize, and complete; for oncology drugs, this can take 8–10 years. Long timelines are expensive and delay innovative therapies from reaching patients. Delays often arise from study startup, a process that can take 6 months or more. We assessed how study-specific factors affected the study startup duration and the resulting overall success of the study. Data from The University of Kansas Cancer Center (KUCC) were used to analyze studies initiated from 2018 to 2022. Accrual percentage was computed based on the number of enrolled participants and the desired enrollment goal. Accrual success was determined by comparing the percentage of enrollments to predetermined threshold values (50%, 70%, or 90%). Studies that achieve or surpass the 70%…
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Taxonomy
TopicsEthics in Clinical Research · Health Systems, Economic Evaluations, Quality of Life · Statistical Methods in Clinical Trials
