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CD22-directed CAR T-cell therapy induces complete remissions in CD19-directed CAR-refractory large B-cell lymphoma.
Baird, John H; Frank, Matthew J; Craig, Juliana; Patel, Shabnum; Spiegel, Jay Y; Sahaf, Bita; Oak, Jean S; Younes, Sheren F; Ozawa, Michael G; Yang, Eric; Natkunam, Yasodha; Tamaresis, John; Ehlinger, Zachary; Reynolds, Warren D; Arai, Sally; Johnston, Laura; Lowsky, Robert; Meyer, Everett; Negrin, Robert S; Rezvani, Andrew R; Shiraz, Parveen; Sidana, Surbhi; Weng, Wen-Kai; Davis, Kara L; Ramakrishna, Sneha; Schultz, Liora; Mullins, Chelsea; Jacob, Allison; Kirsch, Ilan; Feldman, Steven A; Mackall, Crystal L; Miklos, David B; Muffly, Lori.
Afiliação
  • Baird JH; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Frank MJ; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Craig J; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Patel S; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Spiegel JY; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Sahaf B; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Oak JS; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Younes SF; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Ozawa MG; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Yang E; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Natkunam Y; Department of Pathology.
  • Tamaresis J; Department of Pathology.
  • Ehlinger Z; Department of Pathology.
  • Reynolds WD; Department of Pathology.
  • Arai S; Department of Pathology.
  • Johnston L; Department of Biomedical Data Science, and.
  • Lowsky R; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Meyer E; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Negrin RS; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Rezvani AR; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Shiraz P; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Sidana S; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Weng WK; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Davis KL; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Ramakrishna S; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Schultz L; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Mullins C; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Jacob A; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Kirsch I; Center for Cancer Cell Therapy, Stanford Cancer Institute, Stanford University, Stanford, CA.
  • Feldman SA; Division of Blood and Marrow Transplantation, Department of Medicine, Stanford University School of Medicine, Stanford, CA.
  • Mackall CL; Division of Hematology/Oncology, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA; and.
  • Miklos DB; Division of Hematology/Oncology, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA; and.
  • Muffly L; Division of Hematology/Oncology, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA; and.
Blood ; 137(17): 2321-2325, 2021 04 29.
Article em En | MEDLINE | ID: mdl-33512414
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunoterapia Adotiva / Linfoma Difuso de Grandes Células B / Antígenos CD19 / Lectina 2 Semelhante a Ig de Ligação ao Ácido Siálico Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunoterapia Adotiva / Linfoma Difuso de Grandes Células B / Antígenos CD19 / Lectina 2 Semelhante a Ig de Ligação ao Ácido Siálico Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article