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B cell maturation antigen-specific CAR T cells are clinically active in multiple myeloma

Authors :
Cohen, Adam D.
Garfall, Alfred L.
Stadtmauer, Edward A.
Melenhorst, J. Joseph
Lacey, Simon F.
Lancaster, Eric
Vogl, Dan T.
Weiss, Brendan M.
Dengel, Karen
Nelson, Annemarie
Plesa, Gabriela
Chen, Fang
Davis, Megan M.
Hwang, Wei-Ting
Young, Regina M.
Brogdon, Jennifer L.
Isaacs, Randi
Pruteanu-Malinici, Iulian
Siegel, Don L.
Levine, Bruce L.
June, Carl H.
Milone, Michael C.
Source :
Journal of Clinical Investigation. June, 2019, Vol. 129 Issue 6, p2210, 12 p.
Publication Year :
2019

Abstract

BACKGROUND. CAR T cells are a promising therapy for hematologic malignancies. B cell maturation antigen (BCMA) is a rational target in multiple myeloma (MM). METHODS. We conducted a phase I study of autologous T cells lentivirally transduced with a fully human, BCMA-specific CAR containing CD3[zeta] and 4-1BB signaling domains (CART-BCMA), in subjects with relapsed/refractory MM. Twenty-five subjects were treated in 3 cohorts as follows: cohort 1, 1 x [10.sup.8] to 5 x [10.sup.8] CART-BCMA cells alone; cohort 2, cyclophosphamide (Cy) 1.5 g/ [m.sup.2] plus 1 x [10.sup.7] to 5 x [10.sup.7] CART-BCMA cells; cohort 3, Cy 1.5 g/[m.sup.2] plus 1 x [10.sup.8] to 5 x [10.sup.8] CART-BCMA cells. No prespecified BCMA expression level was required. RESULTS. CART-BCMA cells were manufactured and expanded in all subjects. Toxicities included cytokine release syndrome and neurotoxicity, which were grade 3-4 in 8 (32%) and 3 (12%) subjects, respectively, and reversible. One subject died at day 24 from candidemia and progressive myeloma, following treatment for severe cytokine release syndrome and encephalopathy. Responses (based on treated subjects) were seen in 4 of 9 (44%) in cohort 1, 1 of 5 (20%) in cohort 2, and 7 of 11 (64%) in cohort 3, including 5 partial, 5 very good partial, and 2 complete responses, 3 of which were ongoing at 11, 14, and 32 months. Decreased BCMA expression on residual MM cells was noted in responders; expression increased at progression in most. Responses and CART-BCMA expansion were associated with CD4/CD8 T cell ratio and frequency of [CD45RO.sup.-] [CD27.sup.+][CD8.sup.+] T cells in the premanufacturing leukapheresis product. CONCLUSION. CART-BCMA infusions with or without lymphodepleting chemotherapy are clinically active in heavily pretreated patients with MM. TRIAL REGISTRATION. NCT02546167. FUNDING. University of Pennsylvania-Novartis Alliance and NIH.<br />Introduction Despite advances in multiple myeloma (MM) therapy, the disease remains incurable in most patients, and novel approaches are needed. B cell maturation antigen (BCMA) is a cell surface receptor [...]

Details

Language :
English
ISSN :
00219738
Volume :
129
Issue :
6
Database :
Gale General OneFile
Journal :
Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
edsgcl.590449294
Full Text :
https://doi.org/10.1172/JCI126397