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

Authors :
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
Source :
Frontiers in Immunology, Vol 13 (2022)
Publication Year :
2022
Publisher :
Frontiers Media S.A., 2022.

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 registrationhttps://clinicaltrials.gov/ct2/show/NCT03765177, identifier NCT03765177.

Details

Language :
English
ISSN :
16643224
Volume :
13
Database :
Directory of Open Access Journals
Journal :
Frontiers in Immunology
Publication Type :
Academic Journal
Accession number :
edsdoj.ba9bb5ccb69a4646aee78f29aa8e0137
Document Type :
article
Full Text :
https://doi.org/10.3389/fimmu.2022.1074740