Outcomes among adult recipients of CAR T-cell therapy for Burkitt lymphoma

Author:

Samples Laura12ORCID,Sadrzadeh Hossein3,Frigault Matthew J.4,Jacobson Caron A.5,Hamadani Mehdi6ORCID,Gurumurthi Ashwath7ORCID,Strati Paolo7,Shouval Roni8,Noy Ariela8ORCID,Riedell Peter A.9,Dahiya Saurabh10,Maloney David G.12,Till Brian G.12,Hirayama Alexandre V.12ORCID,Gauthier Jordan12ORCID,Gopal Ajay K.12,Smith Stephen D.12ORCID,Poh Christina12,Lynch Ryan12,Ujjani Chaitra12ORCID,Di Mengyang12ORCID,Raghunathan Vikram12,Shakib-Azar Mehrdad1,Naresh Kikkeri N.12,Gooley Ted A.1,Yared Jean11,Jain Michael D.12ORCID,Locke Frederick L.12,Leslie Lori Ann13,Epperla Narendranath14ORCID,Ghosh Monalisa15,Skarbnik Alan16,Hill Brian T.17,Kamdar Manali K.18,Ortiz-Maldonado Valentin19ORCID,Martinez-Cibrian Nuria19ORCID,Shune Leyla20,Shadman Mazyar12ORCID

Affiliation:

1. 1Division of Clinical Research, Fred Hutchinson Cancer Center, Seattle, WA

2. 2Division of Hematology and Oncology, University of Washington, Seattle, WA

3. 3Section of Hematology and Medical Oncology, Boston University Medical Center, Boston, MA

4. 4Center for Cellular Immunotherapy, Massachusetts General Hospital, Boston, MA

5. 5Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA

6. 6Blood and Marrow Transplant and Cellular Therapy, Medical College of Wisconsin, Milwaukee, WI

7. 7Department of Lymphoma/Myeloma, The University of Texas MD Anderson Medical Center, Houston, TX

8. 8Division of Hematologic Malignancies, Memorial Sloan Kettering Cancer Center, New York, NY

9. 9Section of Hematology and Oncology, University of Chicago Medical Center, Chicago, IL

10. 10Blood and Marrow Transplantation and Cellular Therapy, Stanford Cancer Center, Stanford, CA

11. 11Division of Hematology/Oncology, University of Maryland, Baltimore, MD

12. 12Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL

13. 13Division of Lymphoma, John Theurer Cancer Center, Hackensack, NJ

14. 14Division of Hematology, The Ohio State University, Columbus, OH

15. 15Bone Marrow Transplant and Leukemia, University of Michigan, Ann Arbor, MI

16. 16Department of Hematology, Novant Health Cancer Institute, Charlotte, NC

17. 17Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH

18. 18Division of Hematology, University of Colorado Hospital, Aurora, CO

19. 19Oncoimmunotherapy Unit, Department of Hematology, Hospital Clínic de Barcelona, Barcelona, Spain

20. 20Division of Hematologic Malignancies and Cellular Therapeutics, The University of Kansas Medical Center, Kansas City, KS

Abstract

Abstract Burkitt lymphoma (BL) is an aggressive B-cell lymphoma that is associated with poor outcomes in patients with relapsed/refractory disease. This multicenter, retrospective study evaluated real-world CD19 chimeric antigen receptor (CAR) T-cell therapy outcomes in patients with relapsed/refractory BL using data abstracted from the medical records. In total, 31 patients received CAR T cells after a median of 3 previous therapies (range, 1-6). Patients received axicabtagene ciloleucel (n = 19), lisocabtagene maraleucel (n = 4), tisagenlecleucel (n = 4), or other agents (n = 4). Grade 1 to 2 cytokine release syndrome occurred in 83.9% of patients (grade ≥3, 65%), and grade 1 to 2 immune effector cell-associated neurotoxicity syndrome (ICANS) occurred in 29% of patients (grade ≥3, 19.4%). The 28-day mortality rate was 16.1%, including 1 patient who died from grade 5 ICANS. The overall response rate at 1 month was 58.0% with a complete response (CR) rate of 41.9%; however, the 6-month CR rate was only 19.4%. The median progression-free survival was 2.3 months (95% confidence interval, 1.0-9.0), and the median overall survival was 6.0 months (95% confidence interval, 1.9-11.5). Three patients (9.7%) received consolidative allogeneic stem cell transplants, but all subsequently relapsed. In conclusion, CD19 CAR T-cell therapy infrequently delivers long-term disease control in BL. Further investigation is needed to determine the most effective alternative management strategy for these patients.

Publisher

American Society of Hematology

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