CLIC-01: Manufacture and distribution of non-cryopreserved CAR-T cells for patients with CD19 positive hematologic malignancies.

Natasha Kekre,Kevin A Hay,John R Webb,Ranjeeta Mallick,Miruna Balasundaram, Mhairi K Sigrist,Anne-Marie Clement,Julie S Nielsen, Jennifer Quizi,Eric Yung,Scott D Brown,Lisa Dreolini,Daniel D Waller,Julian Smazynski, Nicole S Gierc, Bianca C Loveless, Kayla Clark, Tyler Dyer, Richard Hogg, Leah McCormick, Michael Gignac, Shanti Bell, D Maria Chapman,David Bond, Siao Yong, Rachel Fung,Heather M Lockyer, Victoria Hodgson, Catherine Murphy, Ana Subramanian, Evelyn Wiebe, Piriya Yoganathan, Liana Medynski, Dominique C Vaillan, Alice Black,Sheryl McDiarmid,Michael Kennah,Linda Hamelin,Kevin Song,Sujaatha Narayanan,Judith A Rodrigo,Stefany Dupont,Terry Hawrysh,Justin Presseau,Kednapa Thavorn,Manoj M Lalu,Dean A Fergusson,John C Bell,Harold Atkins,Brad H Nelson,Robert A Holt

Frontiers in immunology(2022)

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摘要
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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关键词
CAR-T cells,hematologic malignancies,immune effector cells,in-house manufacturing,leukaemia,lymphoma,point-of-care manufacturing,prodigy
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