CD22-directed CAR T-cell therapy induces complete remissions in CD19-directed CAR–refractory large B-cell lymphoma
Author(s) -
John H. Baird,
Matthew J. Frank,
Juliana Craig,
Shabnum Patel,
Jay Y. Spiegel,
Bita Sahaf,
Jean Oak,
Sheren Younes,
Michael G. Ozawa,
Eric Yang,
Yasodha Natkunam,
John Tamaresis,
Zachary Ehlinger,
Warren D. Reynolds,
Sally Arai,
Laura Johnston,
Robert Lowsky,
Everett Meyer,
Robert S. Negrin,
Andrew R. Rezvani,
Parveen Shiraz,
Surbhi Sidana,
WenKai Weng,
Kara L. Davis,
Sneha Ramakrishna,
Liora M. Schultz,
Chelsea Mullins,
Allison P. Jacob,
Ilan Kirsch,
Steven A. Feldman,
Crystal L. Mackall,
David B. Miklos,
Lori Muffly
Publication year - 2020
Publication title -
blood
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.515
H-Index - 465
eISSN - 1528-0020
pISSN - 0006-4971
DOI - 10.1182/blood.2020009432
Subject(s) - medicine , refractory (planetary science) , adverse effect , lymphoma , b cell lymphoma , cytokine release syndrome , chimeric antigen receptor , gastroenterology , cd19 , cell therapy , immunology , antigen , oncology , cancer , immunotherapy , cell , biology , astrobiology , genetics
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.
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