CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma

CD19-directed chimeric antigen receptor (CD19CAR) T-cell therapy has been successful in treating several B-cell lineage malignancies, including B-cell non-Hodgkin lymphoma (NHL). This modality has not yet been extended to NHL manifesting in the central nervous system (CNS), primarily as a result of...

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Veröffentlicht in:Blood advances 2021-10, Vol.5 (20), p.4059-4063
Hauptverfasser: Siddiqi, Tanya, Wang, Xiuli, Blanchard, M. Suzette, Wagner, Jamie R., Popplewell, Leslie L., Budde, L. Elizabeth, Stiller, Tracey L., Clark, Mary C., Lim, Laura, Vyas, Vibhuti, Brown, Christine E., Forman, Stephen J.
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container_end_page 4063
container_issue 20
container_start_page 4059
container_title Blood advances
container_volume 5
creator Siddiqi, Tanya
Wang, Xiuli
Blanchard, M. Suzette
Wagner, Jamie R.
Popplewell, Leslie L.
Budde, L. Elizabeth
Stiller, Tracey L.
Clark, Mary C.
Lim, Laura
Vyas, Vibhuti
Brown, Christine E.
Forman, Stephen J.
description CD19-directed chimeric antigen receptor (CD19CAR) T-cell therapy has been successful in treating several B-cell lineage malignancies, including B-cell non-Hodgkin lymphoma (NHL). This modality has not yet been extended to NHL manifesting in the central nervous system (CNS), primarily as a result of concerns for potential toxicity. CD19CAR T cells administered IV are detectable in cerebrospinal fluid (CSF), suggesting that chimeric antigen receptor (CAR) T cells can migrate from the periphery into the CNS, where they can potentially mediate antilymphoma activity. Here, we report the outcome of a subset of patients with primary CNS lymphoma (PCNSL; n = 5) who were treated with CD19CAR T cells in our ongoing phase 1 clinical trial. All patients developed grade ≥ 1 cytokine release syndrome and neurotoxicity post-CAR T-cell infusion; toxicities were reversible and tolerable, and there were no treatment-related deaths. At initial disease response, 3 of 5 patients (60%; 90% confidence interval, 19-92%) seemed to achieve complete remission, as indicated by resolution of enhancing brain lesions; the remaining 2 patients had stable disease. Although the study cohort was small, we demonstrate that using CD19CAR T cells to treat PCNSL can be safe and feasible. This trial was registered at www.clinicaltrials.gov as #NCT02153580. •CD19CAR T-cell therapy for patients with primary CNS lymphoma is feasible and safe.•This case series demonstrates that IV-delivered CD19CAR T cells are promising for the treatment of primary CNS lymphoma.
doi_str_mv 10.1182/bloodadvances.2020004106
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Suzette ; Wagner, Jamie R. ; Popplewell, Leslie L. ; Budde, L. Elizabeth ; Stiller, Tracey L. ; Clark, Mary C. ; Lim, Laura ; Vyas, Vibhuti ; Brown, Christine E. ; Forman, Stephen J.</creator><creatorcontrib>Siddiqi, Tanya ; Wang, Xiuli ; Blanchard, M. Suzette ; Wagner, Jamie R. ; Popplewell, Leslie L. ; Budde, L. Elizabeth ; Stiller, Tracey L. ; Clark, Mary C. ; Lim, Laura ; Vyas, Vibhuti ; Brown, Christine E. ; Forman, Stephen J.</creatorcontrib><description>CD19-directed chimeric antigen receptor (CD19CAR) T-cell therapy has been successful in treating several B-cell lineage malignancies, including B-cell non-Hodgkin lymphoma (NHL). This modality has not yet been extended to NHL manifesting in the central nervous system (CNS), primarily as a result of concerns for potential toxicity. CD19CAR T cells administered IV are detectable in cerebrospinal fluid (CSF), suggesting that chimeric antigen receptor (CAR) T cells can migrate from the periphery into the CNS, where they can potentially mediate antilymphoma activity. Here, we report the outcome of a subset of patients with primary CNS lymphoma (PCNSL; n = 5) who were treated with CD19CAR T cells in our ongoing phase 1 clinical trial. All patients developed grade ≥ 1 cytokine release syndrome and neurotoxicity post-CAR T-cell infusion; toxicities were reversible and tolerable, and there were no treatment-related deaths. At initial disease response, 3 of 5 patients (60%; 90% confidence interval, 19-92%) seemed to achieve complete remission, as indicated by resolution of enhancing brain lesions; the remaining 2 patients had stable disease. Although the study cohort was small, we demonstrate that using CD19CAR T cells to treat PCNSL can be safe and feasible. 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subjects Antigens, CD19
Humans
Immunotherapy, Adoptive
Lymphoma, Non-Hodgkin - therapy
Receptors, Chimeric Antigen
Stimulus Report
T-Lymphocytes
title CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma
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