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Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study

BACKGROUND: Brexucabtagene autoleucel (KTE-X19) is an autologous anti-CD19 CAR T-cell therapy approved in the USA to treat adult patients with relapsed or refractory B-precursor acute lymphoblastic leukemia (R/R B-ALL) based on ZUMA-3 study results. We report updated ZUMA-3 outcomes with longer foll...

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Autores principales: Shah, Bijal D., Ghobadi, Armin, Oluwole, Olalekan O., Logan, Aaron C., Boissel, Nicolas, Cassaday, Ryan D., Leguay, Thibaut, Bishop, Michael R., Topp, Max S., Tzachanis, Dimitrios, O’Dwyer, Kristen M., Arellano, Martha L., Lin, Yi, Baer, Maria R., Schiller, Gary J., Park, Jae H., Subklewe, Marion, Abedi, Mehrdad, Minnema, Monique C., Wierda, William G., DeAngelo, Daniel J., Stiff, Patrick, Jeyakumar, Deepa, Dong, Jinghui, Adhikary, Sabina, Zhou, Lang, Schuberth, Petra C., Faghmous, Imi, Masouleh, Behzad Kharabi, Houot, Roch
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734710/
https://www.ncbi.nlm.nih.gov/pubmed/36494725
http://dx.doi.org/10.1186/s13045-022-01379-0
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author Shah, Bijal D.
Ghobadi, Armin
Oluwole, Olalekan O.
Logan, Aaron C.
Boissel, Nicolas
Cassaday, Ryan D.
Leguay, Thibaut
Bishop, Michael R.
Topp, Max S.
Tzachanis, Dimitrios
O’Dwyer, Kristen M.
Arellano, Martha L.
Lin, Yi
Baer, Maria R.
Schiller, Gary J.
Park, Jae H.
Subklewe, Marion
Abedi, Mehrdad
Minnema, Monique C.
Wierda, William G.
DeAngelo, Daniel J.
Stiff, Patrick
Jeyakumar, Deepa
Dong, Jinghui
Adhikary, Sabina
Zhou, Lang
Schuberth, Petra C.
Faghmous, Imi
Masouleh, Behzad Kharabi
Houot, Roch
author_facet Shah, Bijal D.
Ghobadi, Armin
Oluwole, Olalekan O.
Logan, Aaron C.
Boissel, Nicolas
Cassaday, Ryan D.
Leguay, Thibaut
Bishop, Michael R.
Topp, Max S.
Tzachanis, Dimitrios
O’Dwyer, Kristen M.
Arellano, Martha L.
Lin, Yi
Baer, Maria R.
Schiller, Gary J.
Park, Jae H.
Subklewe, Marion
Abedi, Mehrdad
Minnema, Monique C.
Wierda, William G.
DeAngelo, Daniel J.
Stiff, Patrick
Jeyakumar, Deepa
Dong, Jinghui
Adhikary, Sabina
Zhou, Lang
Schuberth, Petra C.
Faghmous, Imi
Masouleh, Behzad Kharabi
Houot, Roch
author_sort Shah, Bijal D.
collection PubMed
description BACKGROUND: Brexucabtagene autoleucel (KTE-X19) is an autologous anti-CD19 CAR T-cell therapy approved in the USA to treat adult patients with relapsed or refractory B-precursor acute lymphoblastic leukemia (R/R B-ALL) based on ZUMA-3 study results. We report updated ZUMA-3 outcomes with longer follow-up and an extended data set along with contextualization of outcomes to historical standard of care. METHODS: Adults with R/R B-ALL received a single infusion of KTE-X19 (1 × 10(6) CAR T cells/kg). Long-term post hoc subgroup assessments of ZUMA-3 were conducted. Outcomes from matched patients between historical clinical trials and ZUMA-3 patients were assessed in the retrospective historical control study SCHOLAR-3. RESULTS: After 26.8-months median follow-up, the overall complete remission (CR) rate (CR + CR with incomplete hematological recovery) among treated patients (N = 55) in phase 2 was 71% (56% CR rate); medians for duration of remission and overall survival (OS) were 14.6 and 25.4 months, respectively. Most patients responded to KTE-X19 regardless of age or baseline bone marrow blast percentage, but less so in patients with > 75% blasts. No new safety signals were observed. Similar outcomes were observed in a pooled analysis of phase 1 and 2 patients (N = 78). In SCHOLAR-3, the median OS for treated patients from ZUMA-3 (N = 49) and matched historical controls (N = 40) was 25.4 and 5.5 months, respectively. CONCLUSIONS: These data, representing the longest follow-up of CAR T-cell therapy in a multicenter study of adult R/R B-ALL, suggest that KTE-X19 provides a clinically meaningful survival benefit with manageable toxicity in this population. Trial Registration: NCT02614066. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-022-01379-0.
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spelling pubmed-97347102022-12-11 Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study Shah, Bijal D. Ghobadi, Armin Oluwole, Olalekan O. Logan, Aaron C. Boissel, Nicolas Cassaday, Ryan D. Leguay, Thibaut Bishop, Michael R. Topp, Max S. Tzachanis, Dimitrios O’Dwyer, Kristen M. Arellano, Martha L. Lin, Yi Baer, Maria R. Schiller, Gary J. Park, Jae H. Subklewe, Marion Abedi, Mehrdad Minnema, Monique C. Wierda, William G. DeAngelo, Daniel J. Stiff, Patrick Jeyakumar, Deepa Dong, Jinghui Adhikary, Sabina Zhou, Lang Schuberth, Petra C. Faghmous, Imi Masouleh, Behzad Kharabi Houot, Roch J Hematol Oncol Research BACKGROUND: Brexucabtagene autoleucel (KTE-X19) is an autologous anti-CD19 CAR T-cell therapy approved in the USA to treat adult patients with relapsed or refractory B-precursor acute lymphoblastic leukemia (R/R B-ALL) based on ZUMA-3 study results. We report updated ZUMA-3 outcomes with longer follow-up and an extended data set along with contextualization of outcomes to historical standard of care. METHODS: Adults with R/R B-ALL received a single infusion of KTE-X19 (1 × 10(6) CAR T cells/kg). Long-term post hoc subgroup assessments of ZUMA-3 were conducted. Outcomes from matched patients between historical clinical trials and ZUMA-3 patients were assessed in the retrospective historical control study SCHOLAR-3. RESULTS: After 26.8-months median follow-up, the overall complete remission (CR) rate (CR + CR with incomplete hematological recovery) among treated patients (N = 55) in phase 2 was 71% (56% CR rate); medians for duration of remission and overall survival (OS) were 14.6 and 25.4 months, respectively. Most patients responded to KTE-X19 regardless of age or baseline bone marrow blast percentage, but less so in patients with > 75% blasts. No new safety signals were observed. Similar outcomes were observed in a pooled analysis of phase 1 and 2 patients (N = 78). In SCHOLAR-3, the median OS for treated patients from ZUMA-3 (N = 49) and matched historical controls (N = 40) was 25.4 and 5.5 months, respectively. CONCLUSIONS: These data, representing the longest follow-up of CAR T-cell therapy in a multicenter study of adult R/R B-ALL, suggest that KTE-X19 provides a clinically meaningful survival benefit with manageable toxicity in this population. Trial Registration: NCT02614066. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13045-022-01379-0. BioMed Central 2022-12-10 /pmc/articles/PMC9734710/ /pubmed/36494725 http://dx.doi.org/10.1186/s13045-022-01379-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Shah, Bijal D.
Ghobadi, Armin
Oluwole, Olalekan O.
Logan, Aaron C.
Boissel, Nicolas
Cassaday, Ryan D.
Leguay, Thibaut
Bishop, Michael R.
Topp, Max S.
Tzachanis, Dimitrios
O’Dwyer, Kristen M.
Arellano, Martha L.
Lin, Yi
Baer, Maria R.
Schiller, Gary J.
Park, Jae H.
Subklewe, Marion
Abedi, Mehrdad
Minnema, Monique C.
Wierda, William G.
DeAngelo, Daniel J.
Stiff, Patrick
Jeyakumar, Deepa
Dong, Jinghui
Adhikary, Sabina
Zhou, Lang
Schuberth, Petra C.
Faghmous, Imi
Masouleh, Behzad Kharabi
Houot, Roch
Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study
title Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study
title_full Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study
title_fullStr Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study
title_full_unstemmed Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study
title_short Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study
title_sort two-year follow-up of kte-x19 in patients with relapsed or refractory adult b-cell acute lymphoblastic leukemia in zuma-3 and its contextualization with scholar-3, an external historical control study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734710/
https://www.ncbi.nlm.nih.gov/pubmed/36494725
http://dx.doi.org/10.1186/s13045-022-01379-0
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