Can Engagement aid in design and accrual on Clinical Trials? Observations from COMPPARE – A Prospective Comparison of Outcomes with Proton and Photon Radiation in Prostate Cancer.

Publication date: Jul 29, 2026

Slow accrual has been problematic in many clinical trials, especially comparative studies of proton and photon radiation. In addition to proton facility limitation, issues of patient and institutional preferences impact trial accrual. We hypothesized patient engagement could inform the design of a comparative trial with potential for rapid and representative accrual. Previously, we detailed a patient engagement process that identified patient preferences for treatment outcomes and study design for a comparative study of proton and photon therapy in prostate cancer (COMPPARE). We tested the efficacy of this engagement and herein report the resulting design of COMPPARE and its accrual outcomes. Based on patient engagement, COMPPARE was designed as a large prospective comparison of outcomes between parallel cohorts of prostate cancer patients treated pragmatically with protons or photons with a goal of rapid, representative, comparable proton therapy (PT) and intensity-modulated radiation therapy (IMRT) accrual. Site activation required a median of 18 months rather than the planned six months and COVID-19 surges were associated with significant accrual depressions. However, 2524 IMRT and PT patients from 51 institutions were accrued in 52 months to COMPPARE, including 404 Black patients, comprising 16% of the study population, exceeding the goal of 10%. Despite unanticipated delays due to site activation and COVID-19 surges, rapid representative accrual of the large COMPPARE cohorts suggests that a patient engagement process can be highly effective in designing a patient-centric clinical trial.

Concepts Keywords
Cancer cancer outcomes
Prostate particle therapy
Protons prostate cancer
Rapid radiation therapy
Therapy survivorship

Semantics

Type Source Name
disease MESH Prostate Cancer
pathway KEGG Prostate cancer
disease MESH COVID-19
disease MESH cancer

Original Article

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