PROMISE Registry: A prostate cancer registry of outcomes and germline mutations for improved survival and treatment effectiveness.

PROMISE genetic testing germline prostate cancer registry targeted therapy

Journal

The Prostate
ISSN: 1097-0045
Titre abrégé: Prostate
Pays: United States
ID NLM: 8101368

Informations de publication

Date de publication:
14 Nov 2023
Historique:
revised: 09 10 2023
received: 30 07 2023
accepted: 11 10 2023
medline: 15 11 2023
pubmed: 15 11 2023
entrez: 15 11 2023
Statut: aheadofprint

Résumé

Recently approved treatments and updates to genetic testing recommendations for prostate cancer have created a need for correlated analyses of patient outcomes data via germline genetic mutation status. Genetic registries address these gaps by identifying candidates for recently approved targeted treatments, expanding clinical trial data examining specific gene mutations, and understanding effects of targeted treatments in the real-world setting. The PROMISE Registry is a 20-year (5-year recruitment, 15-year follow-up), US-wide, prospective genetic registry for prostate cancer patients. Five thousand patients will be screened through an online at-home germline testing to identify and enroll 500 patients with germline mutations, including: pathogenic or likely pathogenic variants and variants of uncertain significance in genes of interest. Patients will be followed for 15 years and clinical data with real time patient reported outcomes will be collected. Eligible patients will enter long-term follow-up (6-month PRO surveys and medical record retrieval). As a virtual study with patient self-enrollment, the PROMISE Registry may fill gaps in genetics services in underserved areas and for patients within sufficient insurance coverage. The PROMISE Registry opened in May 2021. 2114 patients have enrolled to date across 48 US states and 23 recruiting sites. 202 patients have met criteria for long-term follow-up. PROMISE is on target with the study's goal of 5000 patients screened and 500 patients eligible for long-term follow-up by 2026. The PROMISE Registry is a novel, prospective, germline registry that will collect long-term patient outcomes data to address current gaps in understanding resulting from recently FDA-approved treatments and updates to genetic testing recommendations for prostate cancer. Through inclusion of a broad nationwide sample, including underserved patients and those unaffiliated with major academic centers, the PROMISE Registry aims to provide access to germline genetic testing and to collect data to understand disease characteristics and treatment responses across the disease spectrum for prostate cancer with rare germline genetic variants.

Sections du résumé

BACKGROUND BACKGROUND
Recently approved treatments and updates to genetic testing recommendations for prostate cancer have created a need for correlated analyses of patient outcomes data via germline genetic mutation status. Genetic registries address these gaps by identifying candidates for recently approved targeted treatments, expanding clinical trial data examining specific gene mutations, and understanding effects of targeted treatments in the real-world setting.
METHODS METHODS
The PROMISE Registry is a 20-year (5-year recruitment, 15-year follow-up), US-wide, prospective genetic registry for prostate cancer patients. Five thousand patients will be screened through an online at-home germline testing to identify and enroll 500 patients with germline mutations, including: pathogenic or likely pathogenic variants and variants of uncertain significance in genes of interest. Patients will be followed for 15 years and clinical data with real time patient reported outcomes will be collected. Eligible patients will enter long-term follow-up (6-month PRO surveys and medical record retrieval). As a virtual study with patient self-enrollment, the PROMISE Registry may fill gaps in genetics services in underserved areas and for patients within sufficient insurance coverage.
RESULTS RESULTS
The PROMISE Registry opened in May 2021. 2114 patients have enrolled to date across 48 US states and 23 recruiting sites. 202 patients have met criteria for long-term follow-up. PROMISE is on target with the study's goal of 5000 patients screened and 500 patients eligible for long-term follow-up by 2026.
CONCLUSIONS CONCLUSIONS
The PROMISE Registry is a novel, prospective, germline registry that will collect long-term patient outcomes data to address current gaps in understanding resulting from recently FDA-approved treatments and updates to genetic testing recommendations for prostate cancer. Through inclusion of a broad nationwide sample, including underserved patients and those unaffiliated with major academic centers, the PROMISE Registry aims to provide access to germline genetic testing and to collect data to understand disease characteristics and treatment responses across the disease spectrum for prostate cancer with rare germline genetic variants.

Identifiants

pubmed: 37964482
doi: 10.1002/pros.24650
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : US Department of Defense
ID : W81XWH-18-2-0060
Organisme : US Department of Defense
ID : W81XWH-17-2-0043
Organisme : Advancing Cancer Treatment

Informations de copyright

© 2023 The Authors. The Prostate published by Wiley Periodicals LLC.

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Auteurs

Channing J Paller (CJ)

Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Pedro C Barata (PC)

University Hospitals Seidman Cancer Center, Cleveland, Ohio, USA.

Justin Lorentz (J)

Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Leonard J Appleman (LJ)

University of Pittsburgh Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.

Andrew J Armstrong (AJ)

Duke Cancer Institute Center for Prostate & Urologic Cancers, Durham, North Carolina, USA.

Tiffani A DeMarco (TA)

Inova Translational Medicine Institute, Fairfax, Virginia, USA.

Robert Dreicer (R)

University of Virginia Comprehensive Cancer Center, Charlottesville, Virginia, USA.

Jo Ann B Elrod (JAB)

Fred Hutchinson Cancer Center, Clinical Research Division, Seattle, Washington, USA.

Mark Fleming (M)

Virginia Oncology Associates, Norfolk, Virginia, USA.

Christopher George (C)

Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois, USA.

Elisabeth I Heath (EI)

Department of Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan, USA.

Maha H A Hussain (MHA)

Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, Illinois, USA.

Shifeng Mao (S)

Allegheny Health Network Cancer Institute, Pittsburgh, Pennsylvania, USA.

Rana R McKay (RR)

Department of Oncology, University of California San Diego Moores Cancer Center, La Jolla, California, USA.

Alicia K Morgans (AK)

Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

Matthew Orton (M)

Indiana University Health Arnett Cancer Center, Lafayette, Indiana, USA.

Roberto Pili (R)

Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York, USA.

Elyn Riedel (E)

Prostate Cancer Clinical Trials Consortium, New York, New York, USA.

Biren Saraiya (B)

Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.

Joelle Sigmond (J)

Cleveland Clinic, Akron, Ohio, USA.

Alexandra Sokolova (A)

Oregon Health & Science University Knight Cancer Institute, Portland, Oregon, USA.

Walter M Stadler (WM)

Department of Medicine, The University of Chicago Comprehensive Cancer Center, The University of Chicago Medicine, Chicago, Illinois, USA.

Christina Tran (C)

Prostate Cancer Clinical Trials Consortium, New York, New York, USA.

Natalie Macario (N)

Prostate Cancer Clinical Trials Consortium, New York, New York, USA.

Jacob Vinson (J)

Prostate Cancer Clinical Trials Consortium, New York, New York, USA.

Rebecca Green (R)

Prostate Cancer Clinical Trials Consortium, New York, New York, USA.

Heather H Cheng (HH)

Fred Hutchinson Cancer Center, Clinical Research Division, Seattle, Washington, USA.
University of Washington, Department of Medicine, Seattle, Washington, USA.

Classifications MeSH