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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Main Authors: Berman, E. (Author), Cortes, J. (Author), Croce, K. (Author), DeAngelo, D.J (Author), Deininger, M. (Author), Garasic, J.M (Author), Hall, T. (Author), Hochhaus, A. (Author), Januzzi, J.L (Author), Kantarjian, H. (Author), Kasner, S.E (Author), Kim, D.-W (Author), Mauro, M. (Author), McDonald, V. (Author), Naranjo, D. (Author), Nicolini, F. (Author), Petrie, M.C (Author), Pinilla-Ibarz, J. (Author), Seltzer, J. (Author), Srivastava, S. (Author), Xu, J. (Author)
Format: Article
Language:English
Published: BioMed Central Ltd 2022
Subjects:
Online Access:View Fulltext in Publisher
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020 |a 17568722 (ISSN) 
245 1 0 |a Retrospective analysis of arterial occlusive events in the PACE trial by an independent adjudication committee 
260 0 |b BioMed Central Ltd  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1186/s13045-021-01221-z 
520 3 |a 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). © 2022, The Author(s). 
650 0 4 |a acute lymphoblastic leukemia 
650 0 4 |a acute lymphoblastic leukemia 
650 0 4 |a Acute lymphoblastic leukemia 
650 0 4 |a adult 
650 0 4 |a Adult 
650 0 4 |a aged 
650 0 4 |a Aged 
650 0 4 |a Aged, 80 and over 
650 0 4 |a antineoplastic agent 
650 0 4 |a Antineoplastic Agents 
650 0 4 |a Arterial Occlusive Diseases 
650 0 4 |a artery occlusion 
650 0 4 |a Article 
650 0 4 |a cardiovascular risk 
650 0 4 |a chronic myeloid leukemia 
650 0 4 |a chronic myeloid leukemia 
650 0 4 |a Chronic myeloid leukemia 
650 0 4 |a clinical trial 
650 0 4 |a female 
650 0 4 |a Female 
650 0 4 |a follow up 
650 0 4 |a human 
650 0 4 |a Humans 
650 0 4 |a imidazole derivative 
650 0 4 |a Imidazoles 
650 0 4 |a incidence 
650 0 4 |a Incidence 
650 0 4 |a Leukemia, Myelogenous, Chronic, BCR-ABL Positive 
650 0 4 |a major clinical study 
650 0 4 |a male 
650 0 4 |a Male 
650 0 4 |a middle aged 
650 0 4 |a Middle Aged 
650 0 4 |a peripheral occlusive artery disease 
650 0 4 |a peripheral occlusive artery disease 
650 0 4 |a phase 2 clinical trial 
650 0 4 |a Philadelphia 1 chromosome 
650 0 4 |a ponatinib 
650 0 4 |a ponatinib 
650 0 4 |a Precursor Cell Lymphoblastic Leukemia-Lymphoma 
650 0 4 |a protein kinase inhibitor 
650 0 4 |a Protein Kinase Inhibitors 
650 0 4 |a protein tyrosine kinase inhibitor 
650 0 4 |a pyridazine derivative 
650 0 4 |a Pyridazines 
650 0 4 |a Retrospective Studies 
650 0 4 |a retrospective study 
650 0 4 |a risk factor 
650 0 4 |a Safety 
650 0 4 |a standardization 
650 0 4 |a Tyrosine kinase inhibitor 
650 0 4 |a very elderly 
650 0 4 |a young adult 
650 0 4 |a Young Adult 
700 1 0 |a Berman, E.  |e author 
700 1 0 |a Cortes, J.  |e author 
700 1 0 |a Croce, K.  |e author 
700 1 0 |a DeAngelo, D.J.  |e author 
700 1 0 |a Deininger, M.  |e author 
700 1 0 |a Garasic, J.M.  |e author 
700 1 0 |a Hall, T.  |e author 
700 1 0 |a Hochhaus, A.  |e author 
700 1 0 |a Januzzi, J.L.  |e author 
700 1 0 |a Kantarjian, H.  |e author 
700 1 0 |a Kasner, S.E.  |e author 
700 1 0 |a Kim, D.-W.  |e author 
700 1 0 |a Mauro, M.  |e author 
700 1 0 |a McDonald, V.  |e author 
700 1 0 |a Naranjo, D.  |e author 
700 1 0 |a Nicolini, F.  |e author 
700 1 0 |a Petrie, M.C.  |e author 
700 1 0 |a Pinilla-Ibarz, J.  |e author 
700 1 0 |a Seltzer, J.  |e author 
700 1 0 |a Srivastava, S.  |e author 
700 1 0 |a Xu, J.  |e author 
773 |t Journal of Hematology and Oncology