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CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma.
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.
Affiliation
  • Siddiqi T; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.
  • Wang X; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.
  • Blanchard MS; Department of Computational and Quantitative Medicine/Beckman Research Institute, City of Hope Medical Center, Duarte, CA.
  • Wagner JR; Department of Hematology T-Cell Therapeutics Research Laboratories, City of Hope Medical Center, Duarte, CA; and.
  • Popplewell LL; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.
  • Budde LE; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.
  • Stiller TL; Department of Computational and Quantitative Medicine/Beckman Research Institute, City of Hope Medical Center, Duarte, CA.
  • Clark MC; Department of Clinical and Translational Project Development, City of Hope Medical Center, Duarte, CA.
  • Lim L; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.
  • Vyas V; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.
  • Brown CE; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.
  • Forman SJ; Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA.
Blood Adv ; 5(20): 4059-4063, 2021 10 26.
Article in En | MEDLINE | ID: mdl-34492703
ABSTRACT
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, Non-Hodgkin / Receptors, Chimeric Antigen Limits: Humans Language: En Journal: Blood Adv Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, Non-Hodgkin / Receptors, Chimeric Antigen Limits: Humans Language: En Journal: Blood Adv Year: 2021 Document type: Article Affiliation country: