Tisagenlecleucel CAR T-cell therapy in secondary CNS lymphoma

Author:

Frigault Matthew J.12ORCID,Dietrich Jorg13,Martinez-Lage Maria4ORCID,Leick Mark1ORCID,Choi Bryan D.15,DeFilipp Zachariah12ORCID,Chen Yi-Bin12,Abramson Jeremy16ORCID,Crombie Jennifer7,Armand Philippe7,Nayak Lakshmi7,Panzini Chris1,Riley Lauren S.1,Gallagher Kathleen1,Maus Marcela V.12ORCID

Affiliation:

1. Cellular Immunotherapy Program, Massachusetts General Hospital Cancer Center,

2. Blood and Marrow Transplant Program, Massachusetts General Hospital,

3. Division of Neuro-Oncology, Department of Neurology, Massachusetts General Hospital Cancer Center,

4. Department of Pathology, Massachusetts General Hospital,

5. Department of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, and

6. Center for Lymphoma, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA; and

7. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

Abstract

Abstract Chimeric antigen receptor (CAR) T cells targeting CD19 have emerged as a leading engineered T-cell therapy for relapsed/refractory B-cell non-Hodgkin lymphoma. The phase 1/2 clinical trials that led to US Food and Drug Administration approval excluded patients with central nervous system (CNS) involvement, due to strict eligibility criteria. Here, we report on our institutional experience with 8 secondary CNS lymphoma patients treated with commercial tisagenlecleucel. No patient experienced greater than grade 1 neurotoxicity, and no patient required tocilizumab or steroids for CAR T-cell–mediated toxicities. Biomarker analysis suggested CAR T-cell expansion, despite the absence of systemic disease, and early response assessments demonstrated activity of IV infused CAR T cells within the CNS space.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference13 articles.

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2. Tisagenlecleucel in adult relapsed or refractory diffuse large B-cell lymphoma;Schuster;N Engl J Med,2019

3. Clinical presentation, management, and biomarkers of neurotoxicity after adoptive immunotherapy with CAR T cells;Karschnia;Blood,2019

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5. US Department of Health and Human Services . Common Terminology Criteria for Adverse Events (CTCAE), Version 5.0. https://ctep.cancer.gov/protocolDevelopment/electronic_applications/docs/CTCAE_v5_Quick_Reference_8.5x11.pdf. Accessed 29 July 2019.

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