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

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 public...

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Autores principales: 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., Holt, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806210/
https://www.ncbi.nlm.nih.gov/pubmed/36601119
http://dx.doi.org/10.3389/fimmu.2022.1074740
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author 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.
Holt, Robert A.
author_facet 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.
Holt, Robert A.
author_sort Kekre, Natasha
collection PubMed
description 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 × 10(6) CAR-T cells/kg (range 0.13-3.6 × 10(6)/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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spelling pubmed-98062102023-01-03 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. Holt, Robert A. Front Immunol Immunology 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 × 10(6) CAR-T cells/kg (range 0.13-3.6 × 10(6)/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. Frontiers Media S.A. 2022-12-19 /pmc/articles/PMC9806210/ /pubmed/36601119 http://dx.doi.org/10.3389/fimmu.2022.1074740 Text en Copyright © 2022 Kekre, Hay, Webb, Mallick, Balasundaram, Sigrist, Clement, Nielsen, Quizi, Yung, Brown, Dreolini, Waller, Smazynski, Gierc, Loveless, Clark, Dyer, Hogg, McCormick, Gignac, Bell, Chapman, Bond, Yong, Fung, Lockyer, Hodgson, Murphy, Subramanian, Wiebe, Yoganathan, Medynski, Vaillan, Black, McDiarmid, Kennah, Hamelin, Song, Narayanan, Rodrigo, Dupont, Hawrysh, Presseau, Thavorn, Lalu, Fergusson, Bell, Atkins, Nelson and Holt https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
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.
Holt, Robert A.
CLIC-01: Manufacture and distribution of non-cryopreserved CAR-T cells for patients with CD19 positive hematologic malignancies
title CLIC-01: Manufacture and distribution of non-cryopreserved CAR-T cells for patients with CD19 positive hematologic malignancies
title_full CLIC-01: Manufacture and distribution of non-cryopreserved CAR-T cells for patients with CD19 positive hematologic malignancies
title_fullStr CLIC-01: Manufacture and distribution of non-cryopreserved CAR-T cells for patients with CD19 positive hematologic malignancies
title_full_unstemmed CLIC-01: Manufacture and distribution of non-cryopreserved CAR-T cells for patients with CD19 positive hematologic malignancies
title_short CLIC-01: Manufacture and distribution of non-cryopreserved CAR-T cells for patients with CD19 positive hematologic malignancies
title_sort clic-01: manufacture and distribution of non-cryopreserved car-t cells for patients with cd19 positive hematologic malignancies
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806210/
https://www.ncbi.nlm.nih.gov/pubmed/36601119
http://dx.doi.org/10.3389/fimmu.2022.1074740
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