Cited by 10CAR-T cell therapy researchT-cell and B-cell ImmunologyLymphoma Diagnosis and Treatment

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Recovery of humoral immunity in patients with durable complete responses following chimeric antigen receptor modified t cells directed against CD19 (CTL019).

Abstract

7564 Background: Autologous T cells genetically modified to express a chimeric antigen receptor with an external anti-CD19 antibody domain, and CD3ζ and 4-1BB signaling domains (CTL019) can achieve remissions in patients (pts) with relapsed/refractory (r/r) CD19+ non-Hodgkin lymphomas (NHL). We studied the effect of this therapy on humoral immunity. Methods: Serial immunoglobulin (Ig) levels were measured in pts with complete response (CR) to CTL019 on a phase II trial. Pts had r/r CD19+ follicular lymphoma (FL), diffuse large B cell lymphoma (DLBCL), or mantle cell lymphoma (MCL). After collection of lymphocytes, pts received lymphodepleting chemotherapy followed 1 - 4 days later by 1 - 5 x 108CTL019 cells intravenously. Response was assessed every 3 months (mo) for 24 mo. Enrollment is reported from Feb 2014 – Nov 2015, survival analyses through Jan 2016. Results: 43 pts enrolled: median age 56 years (range 25-77); female: male ratio 17:26; median prior therapies 4 (range 1-19); prior ASCT 14 (33%). 30 pts received CTL019; 29 are evaluable for response (15 DLBCL; 13 FL; 1 MCL). Best overall response rate is 59% (17/29); CR 52% (15/29); DLBCL CR 40% (6/15); FL CR 69% (9/13). To date, no pt in CR has relapsed (median follow up 14 mo). 2 pts were receiving IV Ig before CTL019; 2 pts started IV Ig after CTL019 for hypogammaglobulinemia with frequent infections. 10 pts (6 DLBCL; 4 FL) in CR > 5 mo (median 17 mo; range 5-21) did not received IV Ig and had no > grade 2 or recurrent infections. Baseline IgG levels were decreased in all 10 pts (median 514 mg/dL; range 200-639; normal > 650), IgA in 6/10 pts (median 46 mg/dL; range 34-134; normal > 50), and IgM in 8/10 pts (median 28 mg/dL; range 8-74; normal > 40). 4/10 pts had IgG recovery to their baseline level (1 pt at 21 mo) or to normal levels at 6, 9, and 15 mo (total % IgG increases: 10%, 19%, 29%, respectively). 2/10 pts had IgA recovery to > baseline levels (total % IgA increases 3% and 17% at 18 mo). 5/10 pts had total % IgM increases: 6% at 18 mo, 13% at 12 mo, 21% at 12 mo, 46% at 9 mo, and 441% at 15 mo. Conclusions: In adult r/r NHL pts, CTL019 cells can induce a sustained CR during which Ig levels may improve. Most pts do not need Ig replacement after CTL019 therapy. Clinical trial information: NCT02030834.

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Crossref · 10.1200/jco.2016.34.15_suppl.7564

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  • Complete response rates of approximately 40 to 70% were observed in patients with non-Hodgkin lymphoma treated with CD19-targeted CAR T-cell therapy.

    “In addition, complete response rates of approximately 40 to 70% were observed in patients with non-Hodgkin lymphoma [76–78].”

    From Clinical use of lentiviral vectors (2018) · cites this paper as [78]

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Metadata

Authors
Schuster, S. J., Svoboda, J., Nasta, S., Chong, E. A., Porter, D. L., Landsburg, D. J., Mato, A. R., Bhoj, V. G., Milone, M., Lacey, S. F., Strelec, L. E., Zhou, A. Y., Melenhorst, J. J., Chew, A., Hasskarl, J., Wasik, M. A., Marcucci, K., Zheng, Z., Levine, B., & June, C. H.
Affiliations
  • Abramson Cancer Center (US)
  • University of Pennsylvania (US)
  • Novartis (Switzerland) (CH)
Venue
Journal of Clinical Oncology
Published
2016-05-20
Volume
34
Issue
15_suppl
Pages
7564-7564
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W2764189930
Cited by
10
References
0
Citations by year
2023: 1 · 2021: 2 · 2020: 1 · 2018: 2 · 2017: 4
Type
conference abstract
Language
en
Open access
closed
Locations
Journal of Clinical Oncology (publishedVersion)
Topics
  • Health Sciences › Medicine › Oncology › CAR-T cell therapy research
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Lymphoma Diagnosis and Treatment
Keywords
tisagenlecleucel, chimeric antigen receptor T cells, CAR T-cell therapy, humoral immunity, immunoglobulin levels, hypogammaglobulinemia, complete response, relapsed/refractory lymphoma, follicular lymphoma, diffuse large B-cell lymphoma, mantle cell lymphoma, intravenous immunoglobulin, infection risk, long-term follow-up, sustained remission

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