| Literature DB >> 32266380 |
Bianca Rocca1, Alberto Tosetto2, Silvia Betti3, Denise Soldati3, Giovanna Petrucci1, Elena Rossi3,4, Andrea Timillero5, Viviana Cavalca6, Benedetta Porro6, Alessandra Iurlo7, Daniele Cattaneo7, Cristina Bucelli7, Alfredo Dragani8, Mauro Di Ianni8, Paola Ranalli8, Francesca Palandri9, Nicola Vianelli9, Eloise Beggiato10, Giuseppe Lanzarone10, Marco Ruggeri2, Giuseppe Carli2, Elena Maria Elli11, Monica Carpenedo11, Maria Luigia Randi12, Irene Bertozzi12, Chiara Paoli13,14, Giorgina Specchia15, Alessandra Ricco15, Alessandro Maria Vannucchi13,14, Francesco Rodeghiero5, Carlo Patrono1, Valerio De Stefano3,4.
Abstract
Essential thrombocythemia (ET) is characterized by abnormal megakaryopoiesis and enhanced thrombotic risk. Once-daily low-dose aspirin is the recommended antithrombotic regimen, but accelerated platelet generation may reduce the duration of platelet cyclooxygenase-1 (COX-1) inhibition. We performed a multicenter double-blind trial to investigate the efficacy of 3 aspirin regimens in optimizing platelet COX-1 inhibition while preserving COX-2-dependent vascular thromboresistance. Patients on chronic once-daily low-dose aspirin (n = 245) were randomized (1:1:1) to receive 100 mg of aspirin 1, 2, or 3 times daily for 2 weeks. Serum thromboxane B2 (sTXB2), a validated biomarker of platelet COX-1 activity, and urinary prostacyclin metabolite (PGIM) excretion were measured at randomization and after 2 weeks, as primary surrogate end points of efficacy and safety, respectively. Urinary TX metabolite (TXM) excretion, gastrointestinal tolerance, and ET-related symptoms were also investigated. Evaluable patients assigned to the twice-daily and thrice-daily regimens showed substantially reduced interindividual variability and lower median (interquartile range) values for sTXB2 (ng/mL) compared with the once-daily arm: 4 (2.1-6.7; n = 79), 2.5 (1.4-5.65, n = 79), and 19.3 (9.7-40; n = 85), respectively. Urinary PGIM was comparable in the 3 arms. Urinary TXM was reduced by 35% in both experimental arms. Patients in the thrice-daily arm reported a higher abdominal discomfort score. In conclusion, the currently recommended aspirin regimen of 75 to 100 once daily for cardiovascular prophylaxis appears to be largely inadequate in reducing platelet activation in the vast majority of patients with ET. The antiplatelet response to low-dose aspirin can be markedly improved by shortening the dosing interval to 12 hours, with no improvement with further reductions (EudraCT 2016-002885-30).Entities:
Year: 2020 PMID: 32266380 DOI: 10.1182/blood.2019004596
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113