Apheresis for chimeric antigen receptor T-cell production in adult lymphoma patients.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
08 2022
Historique:
revised: 09 06 2022
received: 11 04 2022
accepted: 15 06 2022
pubmed: 20 7 2022
medline: 10 8 2022
entrez: 19 7 2022
Statut: ppublish

Résumé

To date, in-depth analysis of leukapheresis products as starting material for CAR T-cell manufacturing, specifically Tisagenlecleucel production, are scarce. In this study, we report on lymphapheresis data for production of Tisagenlecleucel for elderly and pretreated lymphoma patients. Spectra Optia from Terumo BCT, Lakewood, CO, was employed for apheresis using the cMNC program. Apheresis success was defined as meeting a target total nucleated cell (TNC) count of ≥2 × 10 Twenty-three patients (age 37-77 years) and 24 apheresis runs were evaluated. The median CD3-positive lymphocyte count in peripheral blood at the beginning of apheresis was 565 cells/μl (range: 70-1345 cells/μl). Circulating lymphoma cells were detected in one patient prior to apheresis. Target criteria were met in 21 of 23 patients. The median TNC count in the apheresate was 11.2 × 10 Lymphapheresis with the Spectra Optia cMNC program provided a sufficient quantity of CD3-positive lymphocytes for CAR T-cell manufacturing for the majority of patients despite their heavy pretreatment and advanced age. Moreover, we are the first to advocate early pre-emptive lymphocyte collection in DLBCL-NOS patients intended to undergo treatment with Tisagenlecleucel.

Sections du résumé

BACKGROUND
To date, in-depth analysis of leukapheresis products as starting material for CAR T-cell manufacturing, specifically Tisagenlecleucel production, are scarce. In this study, we report on lymphapheresis data for production of Tisagenlecleucel for elderly and pretreated lymphoma patients.
STUDY DESIGN AND METHODS
Spectra Optia from Terumo BCT, Lakewood, CO, was employed for apheresis using the cMNC program. Apheresis success was defined as meeting a target total nucleated cell (TNC) count of ≥2 × 10
RESULTS
Twenty-three patients (age 37-77 years) and 24 apheresis runs were evaluated. The median CD3-positive lymphocyte count in peripheral blood at the beginning of apheresis was 565 cells/μl (range: 70-1345 cells/μl). Circulating lymphoma cells were detected in one patient prior to apheresis. Target criteria were met in 21 of 23 patients. The median TNC count in the apheresate was 11.2 × 10
CONCLUSIONS
Lymphapheresis with the Spectra Optia cMNC program provided a sufficient quantity of CD3-positive lymphocytes for CAR T-cell manufacturing for the majority of patients despite their heavy pretreatment and advanced age. Moreover, we are the first to advocate early pre-emptive lymphocyte collection in DLBCL-NOS patients intended to undergo treatment with Tisagenlecleucel.

Identifiants

pubmed: 35851959
doi: 10.1111/trf.17030
doi:

Substances chimiques

Receptors, Chimeric Antigen 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1602-1611

Informations de copyright

© 2022 The Authors. Transfusion published by Wiley Periodicals LLC on behalf of AABB.

Références

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Auteurs

Dennis Christoph Harrer (DC)

Department of Internal Medicine III, Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.

Martin Heidenreich (M)

Department of Internal Medicine III, Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.

Matthias Alexander Fante (MA)

Department of Internal Medicine III, Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.

Viktoria Müller (V)

Institute for Clinical Chemistry, Laboratory Medicine and Transfusion Medicine, University Hospital Regensburg, Regensburg, Germany.

Viola Haehnel (V)

Institute for Clinical Chemistry, Laboratory Medicine and Transfusion Medicine, University Hospital Regensburg, Regensburg, Germany.

Robert Offner (R)

Institute for Clinical Chemistry, Laboratory Medicine and Transfusion Medicine, University Hospital Regensburg, Regensburg, Germany.

Ralph Burkhardt (R)

Institute for Clinical Chemistry, Laboratory Medicine and Transfusion Medicine, University Hospital Regensburg, Regensburg, Germany.

Wolfgang Herr (W)

Department of Internal Medicine III, Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.

Matthias Edinger (M)

Department of Internal Medicine III, Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.

Daniel Wolff (D)

Department of Internal Medicine III, Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.

Simone Thomas (S)

Department of Internal Medicine III, Hematology and Oncology, University Hospital Regensburg, Regensburg, Germany.
Leibniz Institute for Immunotherapy, Division of Genetic-Immunotherapy, Regensburg, Germany.

Andreas Brosig (A)

Institute for Clinical Chemistry, Laboratory Medicine and Transfusion Medicine, University Hospital Regensburg, Regensburg, Germany.

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