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Impact of race and social determinants of health on outcomes in patients with aggressive B-cell NHL treated with CAR-T therapy.

Authors :
Karmali R
Machhi R
Epperla N
Shouse G
Romancik J
Moyo TK
Kenkre V
Ollila TA
Fitzgerald L
Hess B
David K
Roy I
Zurko J
Chowdhury SM
Annunzio K
Ferdman R
Bhansali RS
Harris EI
Liu J
Nizamuddin I
Ma S
Moreira J
Winter J
Pro B
Stephens DM
Danilov A
Shah NN
Cohen JB
Barta SK
Torka P
Gordon LI
Source :
Blood advances [Blood Adv] 2024 May 28; Vol. 8 (10), pp. 2592-2599.
Publication Year :
2024

Abstract

Abstract: Chimeric antigen receptor (CAR) T-cell (CAR-T) immunotherapy is an effective therapy for relapsed/refractory B-cell non-Hodgkin lymphoma (r/r B-NHL). However, data are limited on the impact of the convergence of race and social determinants of health on outcomes for patients treated with CAR-T therapy. We examined the impact of interactions between race and insurance type on health care use and outcomes in patients treated with CAR-T therapy for aggressive B-NHL. Adult patients with r/r B-NHL treated with CD19 CAR-Ts were identified between 2015 and 2021 across 13 US academic centers. Insurance type, demographic, and clinical data were collected and analyzed. In total, 466 adult patients were included in our analysis. Median follow-up after CAR-T therapy was 12.7 months. Median progression-free survival (mPFS) was longer for Caucasians (11.5 months) than for African Americans (3.5 months; hazard ratio [HR], 1.56 [1.03-2.4]; P = .04) or Asians (2.7 months; HR, 1.7 [1.02-2.67]; P = .04). Differences in median overall survival (mOS) were not significant. For Medicare (n = 206) vs Medicaid (n = 33) vs private insurance (n = 219) vs self-pay (n = 7): mPFS was 15.9 vs 4.2 vs 6.0 vs 0.9 months (P < .001), respectively; and mOS was 31.2 vs 12.8 vs 21.5 vs 3.2 months (P < .001), respectively. Our multicenter retrospective analysis showed that race and insurance status can affect outcomes for patients treated with CAR-T therapy.<br /> (© 2024 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.)

Details

Language :
English
ISSN :
2473-9537
Volume :
8
Issue :
10
Database :
MEDLINE
Journal :
Blood advances
Publication Type :
Academic Journal
Accession number :
38531057
Full Text :
https://doi.org/10.1182/bloodadvances.2023011996