Circulating CAR T-Cells After Treatment With Axicabtagene Ciloleucel in Patients With Relapsed/Refractory Aggressive B-Cell Lymphomas and Its Association to Treatment Outcome
(2026) In European Journal of Haematology p.1-8- Abstract
OBJECTIVES: This study investigates the expansion of CAR T-cells and its association to treatment outcome.
METHODS: Patients with aggressive B-cell lymphomas treated with anti-CD19 CAR T-cell therapy axicabtagene ciloleucel (axi-cel) at Skåne and Sahlgrenska University Hospitals from 2019 to October 2024 were included. CAR T-cells in peripheral blood were measured by flow cytometry. Association between maximum levels of CAR T-cells and response, progression-free survival, overall survival, cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were investigated.
RESULTS: Peak CAR T-cell levels were higher among patients with complete response (CR) at Day 30 (p = 0.013) and at 12... (More)
OBJECTIVES: This study investigates the expansion of CAR T-cells and its association to treatment outcome.
METHODS: Patients with aggressive B-cell lymphomas treated with anti-CD19 CAR T-cell therapy axicabtagene ciloleucel (axi-cel) at Skåne and Sahlgrenska University Hospitals from 2019 to October 2024 were included. CAR T-cells in peripheral blood were measured by flow cytometry. Association between maximum levels of CAR T-cells and response, progression-free survival, overall survival, cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were investigated.
RESULTS: Peak CAR T-cell levels were higher among patients with complete response (CR) at Day 30 (p = 0.013) and at 12 months (p = 0.036). CD8+ CAR T-cells were higher in patients with CR (median 135.7, IQR 52.8-433.9) compared to patients not obtaining CR (median 23.2, IQR 11.1-103.3) (p = 0.003). The ratio of CD4+:CD8+ CAR T-cells was lower in patients obtaining CR (p = 0.046). Patients with CAR T-cells above 52.4 CAR T-cells/μL showed superior progression-free survival (p < 0.001).
CONCLUSION: Our study indicates that CAR T-cell levels after axi-cel correlate to durable response, progression-free survival, and that expansion of CD8+ CAR T-cells might be of specific importance for efficacy. Potentially, CAR T-cell levels may be used to enable early detection of patients with high risk of CAR T-cell treatment failure.
(Less)
- author
- Werne, Louise Olsson
LU
; Elmér, Evelina
LU
; Lisak, Mikael
; Pálmason, Róbert
LU
; Hult, Annika K
LU
; Dykes, Josefina
LU
and Jerkeman, Mats
LU
- organization
- publishing date
- 2026-04-02
- type
- Contribution to journal
- publication status
- epub
- subject
- in
- European Journal of Haematology
- pages
- 1 - 8
- publisher
- Wiley-Blackwell
- external identifiers
-
- pmid:41923554
- scopus:105034854284
- ISSN
- 1600-0609
- DOI
- 10.1111/ejh.70185
- language
- English
- LU publication?
- yes
- additional info
- © 2026 The Author(s). European Journal of Haematology published by John Wiley & Sons Ltd.
- id
- 62925565-5e26-4d87-b45a-da2b6bf2c9d7
- date added to LUP
- 2026-04-23 09:35:53
- date last changed
- 2026-05-22 05:52:07
@article{62925565-5e26-4d87-b45a-da2b6bf2c9d7,
abstract = {{<p>OBJECTIVES: This study investigates the expansion of CAR T-cells and its association to treatment outcome.</p><p>METHODS: Patients with aggressive B-cell lymphomas treated with anti-CD19 CAR T-cell therapy axicabtagene ciloleucel (axi-cel) at Skåne and Sahlgrenska University Hospitals from 2019 to October 2024 were included. CAR T-cells in peripheral blood were measured by flow cytometry. Association between maximum levels of CAR T-cells and response, progression-free survival, overall survival, cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were investigated.</p><p>RESULTS: Peak CAR T-cell levels were higher among patients with complete response (CR) at Day 30 (p = 0.013) and at 12 months (p = 0.036). CD8+ CAR T-cells were higher in patients with CR (median 135.7, IQR 52.8-433.9) compared to patients not obtaining CR (median 23.2, IQR 11.1-103.3) (p = 0.003). The ratio of CD4+:CD8+ CAR T-cells was lower in patients obtaining CR (p = 0.046). Patients with CAR T-cells above 52.4 CAR T-cells/μL showed superior progression-free survival (p < 0.001).</p><p>CONCLUSION: Our study indicates that CAR T-cell levels after axi-cel correlate to durable response, progression-free survival, and that expansion of CD8+ CAR T-cells might be of specific importance for efficacy. Potentially, CAR T-cell levels may be used to enable early detection of patients with high risk of CAR T-cell treatment failure.</p>}},
author = {{Werne, Louise Olsson and Elmér, Evelina and Lisak, Mikael and Pálmason, Róbert and Hult, Annika K and Dykes, Josefina and Jerkeman, Mats}},
issn = {{1600-0609}},
language = {{eng}},
month = {{04}},
pages = {{1--8}},
publisher = {{Wiley-Blackwell}},
series = {{European Journal of Haematology}},
title = {{Circulating CAR T-Cells After Treatment With Axicabtagene Ciloleucel in Patients With Relapsed/Refractory Aggressive B-Cell Lymphomas and Its Association to Treatment Outcome}},
url = {{http://dx.doi.org/10.1111/ejh.70185}},
doi = {{10.1111/ejh.70185}},
year = {{2026}},
}