Chemotherapy-Refractory Diffuse Large B-Cell Lymphoma and Indolent B-Cell Malignancies Can Be Effectively Treated With Autologous T Cells Expressing an Anti-CD19 Chimeric Antigen Receptor
Mary Ann Liebert (United States)
Abstract
Of 15 patients, eight achieved complete remissions (CRs), four achieved partial remissions, one had stable lymphoma, and two were not evaluable for response. CRs were obtained by four of seven evaluable patients with chemotherapy-refractory DLBCL; three of these four CRs are ongoing, with durations ranging from 9 to 22 months. Acute toxicities including fever, hypotension, delirium, and other neurologic toxicities occurred in some patients after infusion of anti-CD19 CAR T cells; these toxicities resolved within 3 weeks after cell infusion. One patient died suddenly as a result of an unknown cause 16 days after cell infusion. CAR T cells were detected in the blood of patients at peak levels, ranging from nine to 777 CAR-positive T cells/μL.
This is the first report to our knowledge of successful treatment of DLBCL with anti-CD19 CAR T cells. These results demonstrate the feasibility and effectiveness of treating chemotherapy-refractory B-cell malignancies with anti-CD19 CAR T cells. The numerous remissions obtained provide strong support for further development of this approach.
Citation impact
- FWCI
- 70.55
- Percentile
- 100%
- References
- 47
Authors
26Topics & keywords
- Medicine
- Fludarabine
- Chimeric antigen receptor
- Cyclophosphamide
- Lymphoma
- Chemotherapy
- Refractory (planetary science)
- Diffuse large B-cell lymphoma
- Good health and well-being
Funding
- UDU.S. Department of Health and Human ServicesAward: HHSN261200800001E
- NINational Institutes of HealthAwards: Contract No. HHSN261200800001E, HHSN261200800001E
- KPKite Pharma
- NCNational Cancer InstituteAwards: No. HHSN261200800001E, Contract No. HHSN261200800001E
- NCNIH Clinical CenterAward: HHSN261200800001E