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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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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). |
format | Online Article Text |
id | pubmed-8734305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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