TY - JOUR
T1 - Benefit-risk profile of cytoreductive drugs along with antiplatelet and antithrombotic therapy after transient ischemic attack or ischemic stroke in myeloproliferative neoplasms
AU - De Stefano, Valerio
AU - Carobbio, Alessandra
AU - Di Lazzaro, Vincenzo
AU - Guglielmelli, Paola
AU - Iurlo, Alessandra
AU - Finazzi, Maria Chiara
AU - Rumi, Elisa
AU - Cervantes, Francisco
AU - Elli, Elena Maria
AU - Randi, Maria Luigia
AU - Griesshammer, Martin
AU - Palandri, Francesca
AU - Bonifacio, Massimiliano
AU - Hernandez-Boluda, Juan Carlos
AU - Cacciola, Rossella
AU - Miroslava, Palova
AU - Carli, Giuseppe
AU - Beggiato, Eloise
AU - Ellis, Martin H.
AU - Musolino, Caterina
AU - Gaidano, Gianluca
AU - Rapezzi, Davide
AU - Tieghi, Alessia
AU - Lunghi, Francesca
AU - Loscocco, Giuseppe Gaetano
AU - Cattaneo, Daniele
AU - Cortelezzi, Agostino
AU - Betti, Silvia
AU - Rossi, Elena
AU - Finazzi, Guido
AU - Censori, Bruno
AU - Cazzola, Mario
AU - Bellini, Marta
AU - Arellano-Rodrigo, Eduardo
AU - Bertozzi, Irene
AU - Sadjadian, Parvis
AU - Vianelli, Nicola
AU - Scaffidi, Luigi
AU - Gomez, Montse
AU - Cacciola, Emma
AU - Vannucchi, Alessandro M.
AU - Barbui, Tiziano
N1 - Publisher Copyright:
© 2018 The Author(s).
PY - 2018/3/1
Y1 - 2018/3/1
N2 - We analyzed 597 patients with myeloproliferative neoplasms (MPN) who presented transient ischemic attacks (TIA, n = 270) or ischemic stroke (IS, n = 327). Treatment included aspirin, oral anticoagulants, and cytoreductive drugs. The composite incidence of recurrent TIA and IS, acute myocardial infarction (AMI), and cardiovascular (CV) death was 4.21 and 19.2%, respectively at one and five years after the index event, an estimate unexpectedly lower than reported in the general population. Patients tended to replicate the first clinical manifestation (hazard ratio, HR: 2.41 and 4.41 for recurrent TIA and IS, respectively); additional factors for recurrent TIA were previous TIA (HR: 3.40) and microvascular disturbances (HR: 2.30); for recurrent IS arterial hypertension (HR: 4.24) and IS occurrence after MPN diagnosis (HR: 4.47). CV mortality was predicted by age over 60 years (HR: 3.98), an index IS (HR: 3.61), and the occurrence of index events after MPN diagnosis (HR: 2.62). Cytoreductive therapy was a strong protective factor (HR: 0.24). The rate of major bleeding was similar to the general population (0.90 per 100 patient-years). In conclusion, the long-term clinical outcome after TIA and IS in MPN appears even more favorable than in the general population, suggesting an advantageous benefit-risk profile of antithrombotic and cytoreductive treatment.
AB - We analyzed 597 patients with myeloproliferative neoplasms (MPN) who presented transient ischemic attacks (TIA, n = 270) or ischemic stroke (IS, n = 327). Treatment included aspirin, oral anticoagulants, and cytoreductive drugs. The composite incidence of recurrent TIA and IS, acute myocardial infarction (AMI), and cardiovascular (CV) death was 4.21 and 19.2%, respectively at one and five years after the index event, an estimate unexpectedly lower than reported in the general population. Patients tended to replicate the first clinical manifestation (hazard ratio, HR: 2.41 and 4.41 for recurrent TIA and IS, respectively); additional factors for recurrent TIA were previous TIA (HR: 3.40) and microvascular disturbances (HR: 2.30); for recurrent IS arterial hypertension (HR: 4.24) and IS occurrence after MPN diagnosis (HR: 4.47). CV mortality was predicted by age over 60 years (HR: 3.98), an index IS (HR: 3.61), and the occurrence of index events after MPN diagnosis (HR: 2.62). Cytoreductive therapy was a strong protective factor (HR: 0.24). The rate of major bleeding was similar to the general population (0.90 per 100 patient-years). In conclusion, the long-term clinical outcome after TIA and IS in MPN appears even more favorable than in the general population, suggesting an advantageous benefit-risk profile of antithrombotic and cytoreductive treatment.
UR - http://www.scopus.com/inward/record.url?scp=85044144947&partnerID=8YFLogxK
U2 - 10.1038/s41408-018-0048-9
DO - 10.1038/s41408-018-0048-9
M3 - Article
SN - 2044-5385
VL - 8
JO - Blood Cancer Journal
JF - Blood Cancer Journal
IS - 3
M1 - 25
ER -