PROMISE: a real-world clinical-genomic database to address knowledge gaps in prostate cancer.

Journal Article (Journal Article;Review)

PURPOSE: Prostate cancer is a heterogeneous disease with variable clinical outcomes. Despite numerous recent approvals of novel therapies, castration-resistant prostate cancer remains lethal. A "real-world" clinical-genomic database is urgently needed to enhance our characterization of advanced prostate cancer and further enable precision oncology. METHODS: The Prostate Cancer Precision Medicine Multi-Institutional Collaborative Effort (PROMISE) is a consortium whose aims are to establish a repository of de-identified clinical and genomic patient data that are linked to patient outcomes. The consortium structure includes a (1) bio-informatics committee to standardize genomic data and provide quality control, (2) biostatistics committee to independently perform statistical analyses, (3) executive committee to review and select proposals of relevant questions for the consortium to address, (4) diversity/inclusion committee to address important clinical questions pertaining to racial disparities, and (5) patient advocacy committee to understand patient perspectives to improve patients' quality of care. RESULTS: The PROMISE consortium was formed by 16 academic institutions in early 2020 and a secure RedCap database was created. The first patient record was entered into the database in April 2020 and over 1000 records have been entered as of early 2021. Data entry is proceeding as planned with the goal to have over 2500 patient records by the end of 2021. CONCLUSIONS: The PROMISE consortium provides a powerful clinical-genomic platform to interrogate and address data gaps that have arisen with increased genomic testing in the clinical management of prostate cancer. The dataset incorporates data from patient populations that are often underrepresented in clinical trials, generates new hypotheses to direct further research, and addresses important clinical questions that are otherwise difficult to investigate in prospective studies.

Full Text

Duke Authors

Cited Authors

  • Koshkin, VS; Patel, VG; Ali, A; Bilen, MA; Ravindranathan, D; Park, JJ; Kellezi, O; Cieslik, M; Shaya, J; Cabal, A; Brown, L; Labriola, M; Graham, LS; Pritchard, C; Tripathi, A; Nusrat, S; Barata, P; Jang, A; Chen, SR; Garje, R; Acharya, L; Hwang, C; Pilling, A; Oh, W; Jun, T; Natesan, D; Nguyen, C; Kilari, D; Pierro, M; Thapa, B; Cackowski, F; Mack, A; Heath, E; Marshall, CH; Tagawa, ST; Halabi, S; Schweizer, MT; Armstrong, A; Dorff, T; Alva, A; McKay, R

Published Date

  • September 2022

Published In

Volume / Issue

  • 25 / 3

Start / End Page

  • 388 - 396

PubMed ID

  • 34363009

Pubmed Central ID

  • PMC9385488

Electronic International Standard Serial Number (EISSN)

  • 1476-5608

Digital Object Identifier (DOI)

  • 10.1038/s41391-021-00433-1

Language

  • eng

Conference Location

  • England