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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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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)
- ORCID
- 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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