Utilization of Autologous Hematopoietic Cell Transplantation Over Time in Multiple Myeloma: A Population-Based Study
Supporting Files
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4 2024
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File Language:
English
Details
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Alternative Title:Clin Lymphoma Myeloma Leuk
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Personal Author:
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Description:Purpose:
Autologous hematopoietic cell transplantation (autoHCT) is associated with survival benefits in multiple myeloma (MM), but utilization remains low and differs by sociodemographic factors. Prior population-based studies have not fully captured autoHCT utilization or examined relationships between sociodemographic factors and autoHCT trends over time.
Patients and Methods:
We used a novel data linkage between the California Cancer Registry, Center for International Blood and Marrow Transplant Research, and hospitalizations to capture autoHCT in a population-based MM cohort (n=29,109; 1991–2016). Due to interactions by treatment era, stratified multivariable Cox proportional hazards regression models determined factors associated with autoHCT.
Results:
The frequency of MM patients who received autoHCT increased from 5.7% (1991–1995) to 27.4% (2011–2016). In models by treatment era, patients with public/no (vs private) health insurance were less likely to receive autoHCT (2011–2016 Medicare Hazard Ratio (HR) 0.70, 95% Confidence Interval (CI) 0.63 – 0.78; Medicaid HR 0.81, CI 0.72 – 0.91; no insurance HR 0.56, CI 0.32–0.99). In each treatment era, Black/African American (vs non-Hispanic White) patients were less likely to receive autoHCT (2011–2016 HR 0.83, CI 0.72 – 0.95). Hispanic patients were less likely to undergo autoHCT, most prominently in the earliest treatment era (1991–1995 HR 0.58, 95%CI: 0.37 – 0.90; 2011–2016 HR 1.07, CI: 0.96–1.19). Patients in lower socioeconomic status neighborhoods were less likely to utilize autoHCT, but differences decreased over time.
Conclusions:
Despite increases in autoHCT utilization, sociodemographic disparities remain. Identifying and mitigating barriers to autoHCT is essential to ensuring more equitable access to this highly effective therapy.
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Subjects:
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Keywords:
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Source:Clin Lymphoma Myeloma Leuk. 24(4):e119-e129
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Pubmed ID:38195324
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Pubmed Central ID:PMC11624524
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Document Type:
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Funding:HHSN261201800009C/CA/NCI NIH HHSUnited States/ ; NU58DP006344/DP/NCCDPHP CDC HHSUnited States/ ; H23 IP000860/IP/NCIRD CDC HHSUnited States/ ; U24 CA076518/CA/NCI NIH HHSUnited States/ ; HHSN261201800015I/CA/NCI NIH HHSUnited States/ ; UL1 TR001860/TR/NCATS NIH HHSUnited States/ ; HHSN261201800032I/CA/NCI NIH HHSUnited States/ ; HHSN261201800015C/CA/NCI NIH HHSUnited States/ ; KL2 TR001859/TR/NCATS NIH HHSUnited States/ ; HHSN261201800009I/CA/NCI NIH HHSUnited States/ ; HHSN261201800032C/CA/NCI NIH HHSUnited States/ ; P30 CA093373/CA/NCI NIH HHSUnited States/
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Volume:24
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Issue:4
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Collection(s):
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Main Document Checksum:urn:sha-512:faa0275a4d5a6a425ee7209cc76765a8d113fbdc603f20c498c52ac6479648dd40a3da388f96cad713d63a98bb0c7354ac1c5495ac308ebfd4f4891e3fea30a4
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Download URL:
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File Type:
Supporting Files
File Language:
English
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