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Retrospective analysis of arterial occlusive events in the PACE trial by an independent adjudication committee

BACKGROUND: The phase 2 PACE (Ponatinib Ph+ ALL and CML Evaluation) trial of ponatinib showed robust long-term benefit in relapsed Philadelphia chromosome-positive (Ph+) leukemia; arterial occlusive events (AOEs) occurred in ≥ 25% of patients based on investigator reporting. However, AOE rates vary...

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Autores principales: Januzzi, James L., Garasic, Joseph M., Kasner, Scott E., McDonald, Vickie, Petrie, Mark C., Seltzer, Jonathan, Mauro, Michael, Croce, Kevin, Berman, Ellin, Deininger, Michael, Hochhaus, Andreas, Pinilla-Ibarz, Javier, Nicolini, Franck, Kim, Dong-Wook, DeAngelo, Daniel J., Kantarjian, Hagop, Xu, Jing, Hall, Tracey, Srivastava, Shouryadeep, Naranjo, Daniel, Cortes, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734305/
https://www.ncbi.nlm.nih.gov/pubmed/34991679
http://dx.doi.org/10.1186/s13045-021-01221-z
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author Januzzi, James L.
Garasic, Joseph M.
Kasner, Scott E.
McDonald, Vickie
Petrie, Mark C.
Seltzer, Jonathan
Mauro, Michael
Croce, Kevin
Berman, Ellin
Deininger, Michael
Hochhaus, Andreas
Pinilla-Ibarz, Javier
Nicolini, Franck
Kim, Dong-Wook
DeAngelo, Daniel J.
Kantarjian, Hagop
Xu, Jing
Hall, Tracey
Srivastava, Shouryadeep
Naranjo, Daniel
Cortes, Jorge
author_facet Januzzi, James L.
Garasic, Joseph M.
Kasner, Scott E.
McDonald, Vickie
Petrie, Mark C.
Seltzer, Jonathan
Mauro, Michael
Croce, Kevin
Berman, Ellin
Deininger, Michael
Hochhaus, Andreas
Pinilla-Ibarz, Javier
Nicolini, Franck
Kim, Dong-Wook
DeAngelo, Daniel J.
Kantarjian, Hagop
Xu, Jing
Hall, Tracey
Srivastava, Shouryadeep
Naranjo, Daniel
Cortes, Jorge
author_sort Januzzi, James L.
collection PubMed
description BACKGROUND: The phase 2 PACE (Ponatinib Ph+ ALL and CML Evaluation) trial of ponatinib showed robust long-term benefit in relapsed Philadelphia chromosome-positive (Ph+) leukemia; arterial occlusive events (AOEs) occurred in ≥ 25% of patients based on investigator reporting. However, AOE rates vary depending on the definitions and reporting approach used. METHODS: To better understand clinically relevant AOEs with ponatinib, an independent cardiovascular adjudication committee reviewed 5-year AOE data from the PACE trial according to a charter-defined process and standardized event definitions. RESULTS: A total of 449 patients with chronic myeloid leukemia (CML) or Ph+ acute lymphoblastic leukemia (ALL) received ponatinib (median age 59 y; 47% female; 93% ≥ 2 prior tyrosine kinase inhibitors (TKIs); median follow-up, 37.3 months). The adjudicated AOE rate (17%) was lower than the non-adjudicated rate (i.e., rate before adjudication; 25%). The only adjudicated AOE in > 2% of patients was peripheral arterial occlusive disease (4%). Exposure-adjusted incidence of newly occurring adjudicated AOEs decreased over time. Patients with multiple baseline cardiovascular risk factors had higher adjudicated AOE rates than those without risk factors. CONCLUSIONS: This independent adjudication study identified lower AOE rates than previously reported, suggesting earlier overestimation that may inaccurately reflect AOE risk with ponatinib. This trial was registered under ClinicalTrials.gov identifier NCT01207440 on September 23, 2010 (https://clinicaltrials.gov/ct2/show/NCT01207440).
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spelling pubmed-87343052022-01-07 Retrospective analysis of arterial occlusive events in the PACE trial by an independent adjudication committee Januzzi, James L. Garasic, Joseph M. Kasner, Scott E. McDonald, Vickie Petrie, Mark C. Seltzer, Jonathan Mauro, Michael Croce, Kevin Berman, Ellin Deininger, Michael Hochhaus, Andreas Pinilla-Ibarz, Javier Nicolini, Franck Kim, Dong-Wook DeAngelo, Daniel J. Kantarjian, Hagop Xu, Jing Hall, Tracey Srivastava, Shouryadeep Naranjo, Daniel Cortes, Jorge J Hematol Oncol Research BACKGROUND: The phase 2 PACE (Ponatinib Ph+ ALL and CML Evaluation) trial of ponatinib showed robust long-term benefit in relapsed Philadelphia chromosome-positive (Ph+) leukemia; arterial occlusive events (AOEs) occurred in ≥ 25% of patients based on investigator reporting. However, AOE rates vary depending on the definitions and reporting approach used. METHODS: To better understand clinically relevant AOEs with ponatinib, an independent cardiovascular adjudication committee reviewed 5-year AOE data from the PACE trial according to a charter-defined process and standardized event definitions. RESULTS: A total of 449 patients with chronic myeloid leukemia (CML) or Ph+ acute lymphoblastic leukemia (ALL) received ponatinib (median age 59 y; 47% female; 93% ≥ 2 prior tyrosine kinase inhibitors (TKIs); median follow-up, 37.3 months). The adjudicated AOE rate (17%) was lower than the non-adjudicated rate (i.e., rate before adjudication; 25%). The only adjudicated AOE in > 2% of patients was peripheral arterial occlusive disease (4%). Exposure-adjusted incidence of newly occurring adjudicated AOEs decreased over time. Patients with multiple baseline cardiovascular risk factors had higher adjudicated AOE rates than those without risk factors. CONCLUSIONS: This independent adjudication study identified lower AOE rates than previously reported, suggesting earlier overestimation that may inaccurately reflect AOE risk with ponatinib. This trial was registered under ClinicalTrials.gov identifier NCT01207440 on September 23, 2010 (https://clinicaltrials.gov/ct2/show/NCT01207440). BioMed Central 2022-01-06 /pmc/articles/PMC8734305/ /pubmed/34991679 http://dx.doi.org/10.1186/s13045-021-01221-z 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
Januzzi, James L.
Garasic, Joseph M.
Kasner, Scott E.
McDonald, Vickie
Petrie, Mark C.
Seltzer, Jonathan
Mauro, Michael
Croce, Kevin
Berman, Ellin
Deininger, Michael
Hochhaus, Andreas
Pinilla-Ibarz, Javier
Nicolini, Franck
Kim, Dong-Wook
DeAngelo, Daniel J.
Kantarjian, Hagop
Xu, Jing
Hall, Tracey
Srivastava, Shouryadeep
Naranjo, Daniel
Cortes, Jorge
Retrospective analysis of arterial occlusive events in the PACE trial by an independent adjudication committee
title Retrospective analysis of arterial occlusive events in the PACE trial by an independent adjudication committee
title_full Retrospective analysis of arterial occlusive events in the PACE trial by an independent adjudication committee
title_fullStr Retrospective analysis of arterial occlusive events in the PACE trial by an independent adjudication committee
title_full_unstemmed Retrospective analysis of arterial occlusive events in the PACE trial by an independent adjudication committee
title_short Retrospective analysis of arterial occlusive events in the PACE trial by an independent adjudication committee
title_sort retrospective analysis of arterial occlusive events in the pace trial by an independent adjudication committee
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734305/
https://www.ncbi.nlm.nih.gov/pubmed/34991679
http://dx.doi.org/10.1186/s13045-021-01221-z
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