| Literature DB >> 33512414 |
John H Baird1,2, Matthew J Frank1,2, Juliana Craig1,2, Shabnum Patel2, Jay Y Spiegel1,2, Bita Sahaf2, Jean S Oak3, Sheren F Younes3, Michael G Ozawa3, Eric Yang3, Yasodha Natkunam3, John Tamaresis4, Zachary Ehlinger2, Warren D Reynolds2, Sally Arai1, Laura Johnston1, Robert Lowsky1, Everett Meyer1,2, Robert S Negrin1, Andrew R Rezvani1, Parveen Shiraz1,2, Surbhi Sidana1,2, Wen-Kai Weng1, Kara L Davis5, Sneha Ramakrishna5, Liora Schultz5, Chelsea Mullins6, Allison Jacob6, Ilan Kirsch6, Steven A Feldman2, Crystal L Mackall1,2,5, David B Miklos1,2, Lori Muffly1,2.
Abstract
The prognosis of patients with large B-cell lymphoma (LBCL) that progresses after treatment with chimeric antigen receptor (CAR) T-cell therapy targeting CD19 (CAR19) is poor. We report on the first 3 consecutive patients with autologous CAR19-refractory LBCL who were treated with a single infusion of autologous 1 × 106 CAR+ T cells per kilogram targeting CD22 (CAR22) as part of a phase 1 dose-escalation study. CAR22 therapy was relatively well tolerated, without any observed nonhematologic adverse events higher than grade 2. After infusion, all 3 patients achieved complete remission, with all responses continuing at the time of last follow-up (mean, 7.8 months; range, 6-9.3). Circulating CAR22 cells demonstrated robust expansion (peak range, 85.4-350 cells per microliter), and persisted beyond 3 months in all patients with continued radiographic responses and corresponding decreases in circulating tumor DNA beyond 6 months after infusion. Further accrual at a higher dose level in this phase 1 dose-escalation study is ongoing and will explore the role of this therapy in patients in whom prior CAR T-cell therapies have failed. This trial is registered on clinicaltrials.gov as #NCT04088890.Entities:
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Year: 2021 PMID: 33512414 PMCID: PMC8085484 DOI: 10.1182/blood.2020009432
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113