Recurrent arterial occlusive events in patients with chronic myeloid leukemia treated with second- and third-generation tyrosine kinase inhibitors and role of secondary prevention.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
01 08 2019
Historique:
received: 08 02 2019
revised: 03 04 2019
accepted: 16 04 2019
pubmed: 29 4 2019
medline: 24 3 2020
entrez: 29 4 2019
Statut: ppublish

Résumé

Risk of death is particularly high in patients with a previous history of arterial occlusive events (AOEs) and the probability for a recurrent event is around 20%. Little is known about recurrent AOE and the role of secondary prevention in patients with Chronic Myeloid Leukemia (CML) with previous AOE, treated with second- and third-generation tyrosine kinase inhibitors (2 We identified a real-life cohort of 57 consecutive adult CML patients treated with 2 The 60-month cumulative incidence rate of recurrent AOEs was 47.8 ± 10.9%. Despite a history of AOE, 10 patients (16%) were not receiving secondary preventative measures. Patients treated with nilotinib and ponatinib showed a higher incidence of recurrent AOEs (76.7 ± 14.3% and 64 ± 20.1%, respectively) than those treated with dasatinib and bosutinib (44 ± 24.2% and 30.5 ± 15.5%, respectively) (p = 0.01). Only treatment with a 2 CML patients with a previous history of AOE treated with 2

Sections du résumé

BACKGROUND
Risk of death is particularly high in patients with a previous history of arterial occlusive events (AOEs) and the probability for a recurrent event is around 20%. Little is known about recurrent AOE and the role of secondary prevention in patients with Chronic Myeloid Leukemia (CML) with previous AOE, treated with second- and third-generation tyrosine kinase inhibitors (2
METHODS
We identified a real-life cohort of 57 consecutive adult CML patients treated with 2
RESULTS
The 60-month cumulative incidence rate of recurrent AOEs was 47.8 ± 10.9%. Despite a history of AOE, 10 patients (16%) were not receiving secondary preventative measures. Patients treated with nilotinib and ponatinib showed a higher incidence of recurrent AOEs (76.7 ± 14.3% and 64 ± 20.1%, respectively) than those treated with dasatinib and bosutinib (44 ± 24.2% and 30.5 ± 15.5%, respectively) (p = 0.01). Only treatment with a 2
CONCLUSION
CML patients with a previous history of AOE treated with 2

Identifiants

pubmed: 31029498
pii: S0167-5273(19)30723-5
doi: 10.1016/j.ijcard.2019.04.051
pii:
doi:

Substances chimiques

Anticoagulants 0
Platelet Aggregation Inhibitors 0
Protein Kinase Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

124-127

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Giovanni Caocci (G)

Hematology Unit, Businco Hospital, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy. Electronic address: giovanni.caocci@unica.it.

Olga Mulas (O)

Hematology Unit, Businco Hospital, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.

Massimiliano Bonifacio (M)

Department of Medicine, Section of Hematology, University of Verona, Verona, Italy.

Elisabetta Abruzzese (E)

Hematology Unit, Sant'Eugenio Hospital Tor Vergata University, Rome, Italy.

Sara Galimberti (S)

Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.

Ester Maria Orlandi (EM)

Division of Hematology, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.

Alessandra Iurlo (A)

Hematology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.

Mario Annunziata (M)

Hematology Unit, Cardarelli Hospital, Naples, Italy.

Luigiana Luciano (L)

Hematology Unit "Federico II" University of Naples, Naples, Italy.

Fausto Castagnetti (F)

Department of Experimental, Diagnostic and Specialty Medicine, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.

Antonella Gozzini (A)

Hematology Unit, AOU Careggi, University of Florence, Florence, Italy.

Fabio Stagno (F)

Hematology Unit, AOU Policlinico -V. Emanuele, Rodolico Hospital, Catania, Italy.

Gianni Binotto (G)

Hematology Unit, University of Padova, Padua, Italy.

Patrizia Pregno (P)

Hematology Unit, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza, Torino, Italy.

Francesco Albano (F)

Department of Emergency and Organ Transplantation - Hematology Section, University of Bari, Bari, Italy.

Bruno Martino (B)

Hematology Unit, Azienda Ospedaliera "Bianchi-Melacrino-Morelli", Reggio Calabria, Italy.

Claudio Fozza (C)

Department of Clinical and Experimental Medicine, University of Sassari, Sassari, Italy.

Luigi Scaffidi (L)

Department of Medicine, Section of Hematology, University of Verona, Verona, Italy.

Malgorzata Monika Trawinska (MM)

Hematology Unit, Sant'Eugenio Hospital Tor Vergata University, Rome, Italy.

Claudia Baratè (C)

Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.

Chiara Elena (C)

Division of Hematology, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.

Daniele Cattaneo (D)

Hematology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.

Emilia Scalzulli (E)

Hematology, Department of Cellular Biotechnologies and Hematology, Sapienza University, Rome, Italy.

Giorgio La Nasa (G)

Hematology Unit, Businco Hospital, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.

Robin Foà (R)

Hematology, Department of Cellular Biotechnologies and Hematology, Sapienza University, Rome, Italy.

Massimo Breccia (M)

Hematology, Department of Cellular Biotechnologies and Hematology, Sapienza University, Rome, Italy.

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