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CLIC-01: Manufacture and distribution of non-cryopreserved CAR-T cells for patients with CD19 positive hematologic malignancies.
Kekre, Natasha; Hay, Kevin A; Webb, John R; Mallick, Ranjeeta; Balasundaram, Miruna; Sigrist, Mhairi K; Clement, Anne-Marie; Nielsen, Julie S; Quizi, Jennifer; Yung, Eric; Brown, Scott D; Dreolini, Lisa; Waller, Daniel D; Smazynski, Julian; Gierc, Nicole S; Loveless, Bianca C; Clark, Kayla; Dyer, Tyler; Hogg, Richard; McCormick, Leah; Gignac, Michael; Bell, Shanti; Chapman, D Maria; Bond, David; Yong, Siao; Fung, Rachel; Lockyer, Heather M; Hodgson, Victoria; Murphy, Catherine; Subramanian, Ana; Wiebe, Evelyn; Yoganathan, Piriya; Medynski, Liana; Vaillan, Dominique C; Black, Alice; McDiarmid, Sheryl; Kennah, Michael; Hamelin, Linda; Song, Kevin; Narayanan, Sujaatha; Rodrigo, Judith A; Dupont, Stefany; Hawrysh, Terry; Presseau, Justin; Thavorn, Kednapa; Lalu, Manoj M; Fergusson, Dean A; Bell, John C; Atkins, Harold; Nelson, Brad H.
Afiliação
  • Kekre N; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Hay KA; Division of Hematology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
  • Webb JR; Division of Hematology, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Mallick R; Terry Fox Laboratory, British Columbia Cancer Research Institute, Vancouver, BC, Canada.
  • Balasundaram M; Vancouver General Hospital, Leukemia and Bone Marrow Transplant Program of British Columbia, Vancouver, BC, Canada.
  • Sigrist MK; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Clement AM; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Nielsen JS; Canada's Michael Smith Genome Sciences Centre, British Columbia Cancer Research Institute, Vancouver, BC, Canada.
  • Quizi J; Terry Fox Laboratory, British Columbia Cancer Research Institute, Vancouver, BC, Canada.
  • Yung E; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Brown SD; Division of Hematology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
  • Dreolini L; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Waller DD; Center for Innovative Cancer Therapeutics, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Smazynski J; Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON, Canada.
  • Gierc NS; Canada's Michael Smith Genome Sciences Centre, British Columbia Cancer Research Institute, Vancouver, BC, Canada.
  • Loveless BC; Canada's Michael Smith Genome Sciences Centre, British Columbia Cancer Research Institute, Vancouver, BC, Canada.
  • Clark K; Canada's Michael Smith Genome Sciences Centre, British Columbia Cancer Research Institute, Vancouver, BC, Canada.
  • Dyer T; Terry Fox Laboratory, British Columbia Cancer Research Institute, Vancouver, BC, Canada.
  • Hogg R; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • McCormick L; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Gignac M; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Bell S; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Chapman DM; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Bond D; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Yong S; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Fung R; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Lockyer HM; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Hodgson V; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Murphy C; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Subramanian A; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Wiebe E; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Yoganathan P; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Medynski L; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Vaillan DC; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Black A; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • McDiarmid S; Conconi Family Immunotherapy Lab, Trev and Joyce Deeley Research Centre, British Columbia Cancer Research Institute, Victoria, BC, Canada.
  • Kennah M; Center for Innovative Cancer Therapeutics, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Hamelin L; Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON, Canada.
  • Song K; Center for Innovative Cancer Therapeutics, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Narayanan S; Center for Innovative Cancer Therapeutics, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Rodrigo JA; Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON, Canada.
  • Dupont S; Division of Hematology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
  • Hawrysh T; Division of Hematology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
  • Presseau J; Division of Hematology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
  • Thavorn K; Division of Hematology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
  • Lalu MM; Vancouver General Hospital, Leukemia and Bone Marrow Transplant Program of British Columbia, Vancouver, BC, Canada.
  • Fergusson DA; Division of Hematology, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
  • Bell JC; Vancouver General Hospital, Leukemia and Bone Marrow Transplant Program of British Columbia, Vancouver, BC, Canada.
  • Atkins H; Vancouver General Hospital, Leukemia and Bone Marrow Transplant Program of British Columbia, Vancouver, BC, Canada.
  • Nelson BH; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Front Immunol ; 13: 1074740, 2022.
Article em En | MEDLINE | ID: mdl-36601119
ABSTRACT
Access to commercial CD19 CAR-T cells remains limited even in wealthy countries like Canada due to clinical, logistical, and financial barriers related to centrally manufactured products. We created a non-commercial academic platform for end-to-end manufacturing of CAR-T cells within Canada's publicly funded healthcare system. We report initial results from a single-arm, open-label study to determine the safety and efficacy of in-house manufactured CD19 CAR-T cells (entitled CLIC-1901) in participants with relapsed/refractory CD19 positive hematologic malignancies. Using a GMP compliant semi-automated, closed process on the Miltenyi Prodigy, T cells were transduced with lentiviral vector bearing a 4-1BB anti-CD19 CAR transgene and expanded. Participants underwent lymphodepletion with fludarabine and cyclophosphamide, followed by infusion of non-cryopreserved CAR-T cells. Thirty participants with non-Hodgkin's lymphoma (n=25) or acute lymphoblastic leukemia (n=5) were infused with CLIC-1901 21 males (70%), median age 66 (range 18-75). Time from enrollment to CLIC-1901 infusion was a median of 20 days (range 15-48). The median CLIC-1901 dose infused was 2.3 × 106 CAR-T cells/kg (range 0.13-3.6 × 106/kg). Toxicity included ≥ grade 3 cytokine release syndrome (n=2) and neurotoxicity (n=1). Median follow-up was 6.5 months. Overall response rate at day 28 was 76.7%. Median progression-free and overall survival was 6 months (95%CI 3-not estimable) and 11 months (95% 6.6-not estimable), respectively. This is the first trial of in-house manufactured CAR-T cells in Canada and demonstrates that administering fresh CLIC-1901 product is fast, safe, and efficacious. Our experience may provide helpful guidance for other jurisdictions seeking to create feasible and sustainable CAR-T cell programs in research-oriented yet resource-constrained settings. Clinical trial registration https//clinicaltrials.gov/ct2/show/NCT03765177, identifier NCT03765177.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Neoplasias Hematológicas Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfoma não Hodgkin / Neoplasias Hematológicas Idioma: En Ano de publicação: 2022 Tipo de documento: Article