Adaptation of the socioecological model to address disparities in engagement of Black men in prostate cancer genetic testing.


Journal

BMC public health
ISSN: 1471-2458
Titre abrégé: BMC Public Health
Pays: England
ID NLM: 100968562

Informations de publication

Date de publication:
18 Sep 2024
Historique:
received: 24 04 2024
accepted: 06 09 2024
medline: 18 9 2024
pubmed: 18 9 2024
entrez: 17 9 2024
Statut: epublish

Résumé

Black men consistently have higher rates of prostate cancer (PCA)- related mortality. Advances in PCA treatment, screening, and hereditary cancer assessment center around germline testing (GT). Of concern is the significant under-engagement of Black males in PCA GT, limiting the benefit of precision therapy and tailored cancer screening despite longstanding awareness of these disparities. To address these critical disparities, the Socioecological Model (SEM) was employed to develop comprehensive recommendations to overcome barriers and implement equitable strategies to engage Black males in PCA GT. Clinical/research experts, national organization leaders, and community stakeholders spanning multiple regions in US and Africa participated in developing a framework for equity in PCA GT grounded in the SEM. A novel mixed-methods approach was employed to generate key areas to be addressed and informed statements for consensus consideration utilizing the modified Delphi model. Statements achieving strong consensus (> =75% agreement) were included in final equity frameworks addressing clinical/community engagement and research engagement. All societal levels of the SEM (interpersonal, institutional, community, and policy/advocacy) must deliver information about PCA GT to Black males that address benefits/limitations, clinical impact, hereditary cancer implications, with acknowledgment of mistrust (mean scores [MS] 4.57-5.00). Interpersonal strategies for information delivery included engagement of family/friends/peers/Black role models to improve education/awareness and overcome mistrust (MS 4.65-5.00). Institutional strategies included diversifying clinical, research, and educational programs and integrating community liaisons into healthcare institutions (MS 4.57-5.00). Community strategies included partnerships with healthcare institutions and visibility of healthcare providers/researchers at community events (MS 4.65-4.91). Policy/advocacy included improving partnerships between advocacy and healthcare/community organizations while protecting patient benefits (MS 4.57-5.00). Media strategies were endorsed for the first time at every level (MS 4.56-5.00). The SEM-based equity frameworks proposed provide the first multidisciplinary strategies dedicated to increase engagement of Black males in PCA GT, which are critical to reduce disparities in PCA-mortality through informing tailored screening, targeted therapy, and cascade testing in families.

Sections du résumé

BACKGROUND BACKGROUND
Black men consistently have higher rates of prostate cancer (PCA)- related mortality. Advances in PCA treatment, screening, and hereditary cancer assessment center around germline testing (GT). Of concern is the significant under-engagement of Black males in PCA GT, limiting the benefit of precision therapy and tailored cancer screening despite longstanding awareness of these disparities. To address these critical disparities, the Socioecological Model (SEM) was employed to develop comprehensive recommendations to overcome barriers and implement equitable strategies to engage Black males in PCA GT.
METHODS METHODS
Clinical/research experts, national organization leaders, and community stakeholders spanning multiple regions in US and Africa participated in developing a framework for equity in PCA GT grounded in the SEM. A novel mixed-methods approach was employed to generate key areas to be addressed and informed statements for consensus consideration utilizing the modified Delphi model. Statements achieving strong consensus (> =75% agreement) were included in final equity frameworks addressing clinical/community engagement and research engagement.
RESULTS RESULTS
All societal levels of the SEM (interpersonal, institutional, community, and policy/advocacy) must deliver information about PCA GT to Black males that address benefits/limitations, clinical impact, hereditary cancer implications, with acknowledgment of mistrust (mean scores [MS] 4.57-5.00). Interpersonal strategies for information delivery included engagement of family/friends/peers/Black role models to improve education/awareness and overcome mistrust (MS 4.65-5.00). Institutional strategies included diversifying clinical, research, and educational programs and integrating community liaisons into healthcare institutions (MS 4.57-5.00). Community strategies included partnerships with healthcare institutions and visibility of healthcare providers/researchers at community events (MS 4.65-4.91). Policy/advocacy included improving partnerships between advocacy and healthcare/community organizations while protecting patient benefits (MS 4.57-5.00). Media strategies were endorsed for the first time at every level (MS 4.56-5.00).
CONCLUSION CONCLUSIONS
The SEM-based equity frameworks proposed provide the first multidisciplinary strategies dedicated to increase engagement of Black males in PCA GT, which are critical to reduce disparities in PCA-mortality through informing tailored screening, targeted therapy, and cascade testing in families.

Identifiants

pubmed: 39289635
doi: 10.1186/s12889-024-20008-8
pii: 10.1186/s12889-024-20008-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2533

Informations de copyright

© 2024. The Author(s).

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Auteurs

Amy E Leader (AE)

Department of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.

Timothy R Rebbeck (TR)

Department of Epidemiology, Harvard TH Chan School of Public Health and Dana-Farber Cancer Institute, Boston, MA, USA.

William K Oh (WK)

Department of Internal Medicine, Mount Sinai Hospital, New York, NY, USA.

Alpa V Patel (AV)

Department of Population Science, American Cancer Society, Atlanta, GA, USA.

Eric P Winer (EP)

Department of Medicine, Yale Cancer Center and Yale School of Medicine, 333 Cedar Street, WWW214A, New Haven, CT, 06520, USA.

LeeAnn O Bailey (LO)

National Cancer Institute/Center to Reduce Cancer Health Disparities, Rockville, MD, USA.

Leonard G Gomella (LG)

Department of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.

Crystal Y Lumpkins (CY)

Department of Communication, Population Sciences Division, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.

Isla P Garraway (IP)

Department of Urology, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
VA Greater Los Angeles Healthcare System, Los Angeles, CA, USA.

Lisa B Aiello (LB)

Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.

Monica L Baskin (ML)

Department of Medicine, UPMC Hillman Cancer Center, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

Heather H Cheng (HH)

Department of Medicine, Fred Hutchinson Cancer Center, University of Washington, Seattle, WA, USA.

Kathleen A Cooney (KA)

Department of Medicine, Duke University School of Medicine and Duke Cancer Institute, Durham, NC, USA.

Amanda Ganzak (A)

Cancer Genetics and Prevention Program, Yale New Haven Hospital, New Haven, CT, USA.

Daniel J George (DJ)

Department of Medicine, Duke University School of Medicine and Duke Cancer Institute, Durham, NC, USA.

Susan Halabi (S)

Department of Biostatistics & Bioinformatics, Duke University School of Medicine, Durham, NC, USA.

Feighanne Hathaway (F)

Department of Medicine, High-Risk and Advanced Prostate Cancer Clinic, University of Chicago Medicine, University of Chicago, Chicago, IL, USA.

Claire Healy (C)

Cancer Genetics and Prevention Program, Yale New Haven Hospital, New Haven, CT, USA.

Joseph W Kim (JW)

Department of Medicine, Yale Cancer Center and Yale School of Medicine, 333 Cedar Street, WWW214A, New Haven, CT, 06520, USA.

Michael S Leapman (MS)

Department of Urology, Yale School of Medicine, New Haven, CT, USA.

Stacy Loeb (S)

Department of Urology and Population Health, New York University and Manhattan Veterans Affairs, New York, NY, USA.

Kara N Maxwell (KN)

Department of Medicine-Hematology/Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Christopher McNair (C)

Department of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.

Todd M Morgan (TM)

Department of Urology, Rogel Cancer Center, University of Michigan, Ann Arbor, MI, USA.

Breanne Prindeville (B)

Neaman Center for Personalized Medicine, NorthShore University Health System, Evanston, IL, USA.

Howard R Soule (HR)

Prostate Cancer Foundation, Santa Monica, CA, USA.

Whitney L Steward (WL)

National Cancer Institute/Center to Reduce Cancer Health Disparities, Rockville, MD, USA.

Sakinah C Suttiratana (SC)

Department of Medicine, Yale Cancer Center and Yale School of Medicine, 333 Cedar Street, WWW214A, New Haven, CT, 06520, USA.

Mary-Ellen Taplin (ME)

Department of Medicine, Dana-Farber Cancer Institute, Boston, MA, USA.

Kosj Yamoah (K)

Departmetnt of Radiation Oncology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.

Thierry Fortune (T)

Department of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.

Kris Bennett (K)

Movember, Santa Monica, CA, USA.

Joshua Blanding-Godbolt (J)

Department of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.

Laura Gross (L)

Department of Medicine, Yale University and Yale Cancer Center, New Haven, CT, USA.

Veda N Giri (VN)

Department of Medicine, Yale Cancer Center and Yale School of Medicine, 333 Cedar Street, WWW214A, New Haven, CT, 06520, USA. Veda.Giri@yale.edu.

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