Impaired hematopoiesis affects apheresis and <scp>CAR</scp> T‐cell product composition and treatment response

BACKGROUND: T-cell yields during leukapheresis. This can be difficult in heavily pretreated patients, who often show leukopenia and reduced T-cell fitness. METHODS: We analyzed 166 leukapheresis products from 154 patients undergoing manufacturing of CD19-directed CAR T-cells, including 146 from non-Hodgkin's lymphoma (NHL) and 20 from acute lymphoblastic leukemia (ALL). Collections were performed for commercial CAR T-cell products (axi-cel, tisa-cel, brexu-cel, liso-cel; n = 121) and the HD-CAR-1 trial with in-house manufacturing (heidagenlecleucel; n = 45). RESULTS: CAR T-cells in the product correlated with improved clinical outcomes (p = .04; p = .023). CONCLUSION: These findings highlight the importance of early leukapheresis, ideally before intensive treatments, to optimize T-cell yield, product quality, and therapeutic efficacy.

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Publication Details

Journal
Transfusion
Published
2026-04-10
DOI
https://doi.org/10.1111/trf.70224
Primary Topic
CAR-T cell therapy research
Type
article
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article

Impaired hematopoiesis affects apheresis and CAR T‐cell product composition and treatment response

Brigitte Neuber, Maria‐Luisa Schubert, Angela Hückelhoven‐Krauss, Felix Korell et al.
Transfusion
CAR-T cell therapy research
article

Impaired hematopoiesis affects apheresis and CAR T‐cell product composition and treatment response

Brigitte Neuber, Maria‐Luisa Schubert, Angela Hückelhoven‐Krauss, Felix Korell, Patrick Derigs, Carsten Müller‐Tidow, Anita Ludwig‐Husemann, Miriam Stenzinger, Sandra Sauer, Tim Sauer, Anita Schmitt, Kiavasch Farid, Hanna Kuhn, Peter Dreger, Michael Schmitt
article en

Abstract

BACKGROUND: T-cell yields during leukapheresis. This can be difficult in heavily pretreated patients, who often show leukopenia and reduced T-cell fitness. METHODS: We analyzed 166 leukapheresis products from 154 patients undergoing manufacturing of CD19-directed CAR T-cells, including 146 from non-Hodgkin's lymphoma (NHL) and 20 from acute lymphoblastic leukemia (ALL). Collections were performed for commercial CAR T-cell products (axi-cel, tisa-cel, brexu-cel, liso-cel; n = 121) and the HD-CAR-1 trial with in-house manufacturing (heidagenlecleucel; n = 45). RESULTS: CAR T-cells in the product correlated with improved clinical outcomes (p = .04; p = .023). CONCLUSION: These findings highlight the importance of early leukapheresis, ideally before intensive treatments, to optimize T-cell yield, product quality, and therapeutic efficacy.

Transfusion
Heidelberg University (DE), University Hospital Heidelberg (DE), Institute for Transfusion Medicine (US)
Zero hunger
Openalex Percentile: Top 25%
CAR-T cell therapy research
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