| Literature DB >> 31689242 |
Susan Prockop1,2, Ekaterina Doubrovina1,3, Stephanie Suser1, Glenn Heller4, Juliet Barker5,6, Parastoo Dahi5,6, Miguel A Perales5,6, Esperanza Papadopoulos5,6, Craig Sauter5,6, Hugo Castro-Malaspina5,6, Farid Boulad1,2, Kevin J Curran1,2, Sergio Giralt5,6, Boglarka Gyurkocza5,6, Katharine C Hsu5,6, Ann Jakubowski5,6, Alan M Hanash5,6, Nancy A Kernan1,2, Rachel Kobos1,7, Guenther Koehne8, Heather Landau5,6, Doris Ponce5,6, Barbara Spitzer1,2, James W Young5,6, Gerald Behr9, Mark Dunphy9, Sofia Haque9, Julie Teruya-Feldstein10, Maria Arcila11, Christine Moung11, Susan Hsu12, Aisha Hasan1,13, Richard J O'Reilly1,2.
Abstract
BACKGROUNDAdoptive transfer of donor-derived EBV-specific cytotoxic T-lymphocytes (EBV-CTLs) can eradicate EBV-associated lymphomas (EBV-PTLD) after transplantation of hematopoietic cell (HCT) or solid organ (SOT) but is unavailable for most patients.METHODSWe developed a third-party, allogeneic, off-the-shelf bank of 330 GMP-grade EBV-CTL lines from specifically consented healthy HCT donors. We treated 46 recipients of HCT (n = 33) or SOT (n = 13) with established EBV-PTLD, who had failed rituximab therapy, with third-party EBV-CTLs. Treatment cycles consisted of 3 weekly infusions of EBV-CTLs and 3 weeks of observation.RESULTSEBV-CTLs did not induce significant toxicities. One patient developed grade I skin graft-versus-host disease. Complete remission (CR) or sustained partial remission (PR) was achieved in 68% of HCT recipients and 54% of SOT recipients. For patients who achieved CR/PR or stable disease after cycle 1, one year overall survival was 88.9% and 81.8%, respectively. In addition, 3 of 5 recipients with POD after a first cycle who received EBV-CTLs from a different donor achieved CR or durable PR (60%) and survived longer than 1 year. Maximal responses were achieved after a median of 2 cycles.CONCLUSIONThird-party EBV-CTLs of defined HLA restriction provide safe, immediately accessible treatment for EBV-PTLD. Secondary treatment with EBV-CTLs restricted by a different HLA allele (switch therapy) can also induce remissions if initial EBV-CTLs are ineffective. These results suggest a promising potential therapy for patients with rituximab-refractory EBV-associated lymphoma after transplantation.TRIAL REGISTRATIONPhase II protocols (NCT01498484 and NCT00002663) were approved by the Institutional Review Board at Memorial Sloan Kettering Cancer Center, the FDA, and the National Marrow Donor Program.FUNDINGThis work was supported by NIH grants CA23766 and R21CA162002, the Aubrey Fund, the Claire Tow Foundation, the Major Family Foundation, the Max Cure Foundation, the Richard "Rick" J. Eisemann Pediatric Research Fund, the Banbury Foundation, the Edith Robertson Foundation, and the Larry Smead Foundation. Atara Biotherapeutics licensed the bank of third-party EBV-CTLs from Memorial Sloan Kettering Cancer Center in June 2015.Entities:
Keywords: Cancer immunotherapy; Immunology; T cells; Transplantation
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Year: 2020 PMID: 31689242 PMCID: PMC6994129 DOI: 10.1172/JCI121127
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808