Visualizing Geographic Variation and Systemic Inequities of Disease Burden and CAR T-cell Therapy Access in Multiple Myeloma in the US

Chimeric antigen receptor (CAR) T-cell therapies have emerged as a transformative treatment for relapsed/refractory multiple myeloma (RRMM). Despite substantial survival benefits, access to CAR T remains limited across many US regions, especially in underserved areas. This study characterizes geographic variation in multiple myeloma (MM) burden and identifies key drivers of the disparity in CAR T access to inform targeted strategies in closing access gaps. MM burden from January 2021–August 2024 was estimated using the Komodo Patient-Level Analytics and Insights Derivative (PLAID) claims database. Patients with MM and CAR T recipients were identified using International Classification of Diseases-10 and billing codes, respectively. MM prevalence at ZIP-3 level (first 3 digits of ZIP) was derived from the US Cancer Statistics (USCS) database. Distance and drive-time to the nearest authorized treatment center (ATC) for patients with MM and drive-time to ATCs for CAR T recipients were calculated and compared nationally and by region. There were 106,593 unique prevalent MM cases over the study period. CAR T recipients were slightly younger but otherwise similar to the overall MM population across sex, regions, and insurance type (Table 1). MM burden was highest in the South (66/100,000) and Northeast (67/100,000), with hotspots in Florida, Mississippi, and New Jersey (Fig 1). While 72.9% of patients overall lived within 50 miles of an ATC, this dropped to 67.0% in the South and 66.7% in the Midwest. Median drive-time for CAR T recipients to the ATCs where they received treatment was the longest in the South (1.5 hours) compared to the national estimate (1.3 hours). This suggests CAR T recipients often traveled farther than necessary, since the median drive-time to the nearest ATC was 0.7 hour for patients with MM in general (Fig 2). Supporting this, 36.6% CAR T recipients skipped one of their top three nearest ATCs. CAR T recipients in non-metropolitan areas faced longer median drive-times (2.8 hours) compared to metropolitan areas (1.1 hours). Overall, 15.1% CAR T recipients traveled out-of-state, 2+ hours, and to a non-top three nearest ATC, with this group more likely to be from the South, non-metro areas, and insured under Medicare fee-for-service. This study highlights geographic disparities in MM burden and CAR T access. MM prevalence was highest in the South and Northeast, while access barriers—distance, drive-time, and out-of-state travel—were more pronounced in the South and Midwest. Many CAR T recipients bypassed closer ATCs, indicating systemic or referral-related barriers. These findings highlight areas needing targeted efforts to close access gaps and improve equity in CAR T referral and utilization. Further analyses of sociodemographic drivers of CAR T utilization in RRMM are ongoing and will be presented.

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Publication Details

Journal
Transplantation and Cellular Therapy
Published
2026-02-01
DOI
https://doi.org/10.1016/j.jtct.2025.12.427
Primary Topic
CAR-T cell therapy research
Type
article
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article

Visualizing Geographic Variation and Systemic Inequities of Disease Burden and CAR T-cell Therapy Access in Multiple Myeloma in the US

Jie Ting, Benjamin Avi Derman, Brandon Jamaal Blue, Kian Farajkhah et al.
Transplantation and Cellular Therapy
CAR-T cell therapy research
article

Visualizing Geographic Variation and Systemic Inequities of Disease Burden and CAR T-cell Therapy Access in Multiple Myeloma in the US

Jie Ting, Benjamin Avi Derman, Brandon Jamaal Blue, Kian Farajkhah, Andrew ElHabr, Ken Hasegawa, Attaya Suvannasankha, Zizi Elsisi, Turgay Ayer, Avik Ray
article en

Abstract

Chimeric antigen receptor (CAR) T-cell therapies have emerged as a transformative treatment for relapsed/refractory multiple myeloma (RRMM). Despite substantial survival benefits, access to CAR T remains limited across many US regions, especially in underserved areas. This study characterizes geographic variation in multiple myeloma (MM) burden and identifies key drivers of the disparity in CAR T access to inform targeted strategies in closing access gaps. MM burden from January 2021–August 2024 was estimated using the Komodo Patient-Level Analytics and Insights Derivative (PLAID) claims database. Patients with MM and CAR T recipients were identified using International Classification of Diseases-10 and billing codes, respectively. MM prevalence at ZIP-3 level (first 3 digits of ZIP) was derived from the US Cancer Statistics (USCS) database. Distance and drive-time to the nearest authorized treatment center (ATC) for patients with MM and drive-time to ATCs for CAR T recipients were calculated and compared nationally and by region. There were 106,593 unique prevalent MM cases over the study period. CAR T recipients were slightly younger but otherwise similar to the overall MM population across sex, regions, and insurance type (Table 1). MM burden was highest in the South (66/100,000) and Northeast (67/100,000), with hotspots in Florida, Mississippi, and New Jersey (Fig 1). While 72.9% of patients overall lived within 50 miles of an ATC, this dropped to 67.0% in the South and 66.7% in the Midwest. Median drive-time for CAR T recipients to the ATCs where they received treatment was the longest in the South (1.5 hours) compared to the national estimate (1.3 hours). This suggests CAR T recipients often traveled farther than necessary, since the median drive-time to the nearest ATC was 0.7 hour for patients with MM in general (Fig 2). Supporting this, 36.6% CAR T recipients skipped one of their top three nearest ATCs. CAR T recipients in non-metropolitan areas faced longer median drive-times (2.8 hours) compared to metropolitan areas (1.1 hours). Overall, 15.1% CAR T recipients traveled out-of-state, 2+ hours, and to a non-top three nearest ATC, with this group more likely to be from the South, non-metro areas, and insured under Medicare fee-for-service. This study highlights geographic disparities in MM burden and CAR T access. MM prevalence was highest in the South and Northeast, while access barriers—distance, drive-time, and out-of-state travel—were more pronounced in the South and Midwest. Many CAR T recipients bypassed closer ATCs, indicating systemic or referral-related barriers. These findings highlight areas needing targeted efforts to close access gaps and improve equity in CAR T referral and utilization. Further analyses of sociodemographic drivers of CAR T utilization in RRMM are ongoing and will be presented.

Transplantation and Cellular TherapyVol. 32(2)
Indiana University Health (US), Moffitt Cancer Center (US), University of Chicago Medical Center (US), Systems Analytics (United States) (US), CardioDx (United States) (US), Indiana Cancer Consortium (US), Indiana University – Purdue University Indianapolis (US)
Openalex Percentile: Top 67%
CAR-T cell therapy research
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