Donor origin CAR T cells: graft versus malignancy effect without GVHD, a systematic review

Author:

Anwer Faiz12,Shaukat Al-Aman3,Zahid Umar45,Husnain Muhammad4,McBride Ali6,Persky Daniel12,Lim Melissa2,Hasan Nida7,Riaz Irbaz Bin4

Affiliation:

1. Department of Medicine, Hematology & Oncology, University of Arizona, Tucson, AZ, USA

2. Arizona Cancer Center, University of Arizona, Tucson, AZ, USA

3. James Paget University Hospital, Norfolk, UK

4. Department of Medicine, University of Arizona, Tucson, AZ, USA

5. College of Public Health, University of Arizona, Tucson, AZ, USA

6. College of Pharmacy, University of Arizona, Tucson, AZ, USA

7. University of Arizona Zuckerman College of Public Health, Tucson, AZ, USA

Abstract

CD19, CD20 chimeric antigen receptor T (CAR T) cell therapy has shown promising results for the treatment of relapsed or refractory hematological malignancies. Best results have been reported in acute lymphoblastic leukemia patients with a complete response rate above 80%. Patients who received donor-derived CAR T cells for the relapsed malignancy after stem cell transplantation (allogenic hematopoietic stem cell transplant) were identified from the published trials. A total of 72 patients from seven studies were treated with donor-derived CAR T cells. Only five out of 72 patients (6.9%) developed graft versus host disease. Use of donor-derived CAR T cell for relapse prophylaxis, minimal residual disease clearance or salvage from relapse is therefore highly effective, and risk of graft versus host disease flare is very low. Side effects include cytokine release syndrome, tumor lysis syndrome, B-cell aplasia along with CNS toxicity.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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