Jonathan Tyes, Christie Okoye, Christy Houde, Jay Hydren, Mason Barnes, Rachel Jensen, Jenny Ahlstrom, Jeffrey Zonder, Craig Cole
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引用次数: 0
Abstract
Background
Bi-specific antibody therapy represents a promising advancement in the treatment of multiple myeloma, offering targeted, off-the-shelf immunotherapy that may be more accessible than other cellular therapies. However, barriers such as treatment cost, complex care coordination, and the need for frequent clinical visits may still limit equitable access. Black patients—who experience higher incidence and earlier onset of multiple myeloma may face disproportionate challenges in receiving this therapy. While systemic inequities in cancer care are well documented, limited research has explored how patient-level perceptions, experiences, and social determinants influence access to bi-specific antibody treatment.
Objective
This study aims to characterize disparities in access to bi-specific antibody therapy among patients with multiple myeloma, with particular attention to race, ethnicity, socioeconomic status, and social determinants of health. It also seeks to explore how these factors shape patient satisfaction, treatment decision-making, and perceived barriers to care.
Methods
This is a prospective, cross-sectional survey study involving patients with a diagnosis of multiple myeloma, including those who are eligible for or have received bi-specific antibody therapy. Participants will be drawn from the HealthTree research registry and invited to complete a 25–35-minute electronic survey containing up to 46 questions. Topics include treatment access, care navigation, perceived barriers, and patient-reported outcomes. An additional 11 items will capture demographic and socioeconomic data, including race/ethnicity, education, insurance coverage, and neighborhood-level indicators. Descriptive statistics and comparative analyses (e.g., chi-square tests, t-tests, ANOVA) will be used, along with multivariable modeling to examine associations between social determinants and disparities in access and outcomes.
Results (Trial in Progress)
As of June 2025, survey data collection is ongoing, with preliminary responses received from a diverse cohort of participants in the HealthTree registry.
Discussion
This study will generate real-world, patient-centered data on inequities in access to bi-specific antibody therapy for multiple myeloma. By incorporating lived experiences and perceptions, the findings aim to inform policy, improve provider awareness, and guide system-level changes to promote more equitable delivery of this emerging treatment modality
期刊介绍:
Journal of the National Medical Association, the official journal of the National Medical Association, is a peer-reviewed publication whose purpose is to address medical care disparities of persons of African descent.
The Journal of the National Medical Association is focused on specialized clinical research activities related to the health problems of African Americans and other minority groups. Special emphasis is placed on the application of medical science to improve the healthcare of underserved populations both in the United States and abroad. The Journal has the following objectives: (1) to expand the base of original peer-reviewed literature and the quality of that research on the topic of minority health; (2) to provide greater dissemination of this research; (3) to offer appropriate and timely recognition of the significant contributions of physicians who serve these populations; and (4) to promote engagement by member and non-member physicians in the overall goals and objectives of the National Medical Association.