Alvarez-Larrán Alberto, Pereira Arturo, Guglielmelli Paola, Hernández-Boluda Juan Carlos, Arellano-Rodrigo Eduardo, Ferrer-Marín Francisca, Samah Alimam, Griesshammer Martin, Kerguelen Ana, Andreasson Bjorn, Burgaleta Carmen, Schwarz Jiri, García-Gutiérrez Valentín, Ayala Rosa, Barba Pere, Gómez-Casares María Teresa, Paoli Chiara, Drexler Beatrice, Zweegman Sonja, McMullin Mary F, Samuelsson Jan, Harrison Claire, Cervantes Francisco, Vannucchi Alessandro M, Besses Carlos
Hematology Department, Hospital del Mar, IMIM, UAB, Barcelona, Spain
Hematotherapy and Hemostasis Department, Hospital Clínic, Barcelona, Spain.
Haematologica. 2016 Aug;101(8):926-31. doi: 10.3324/haematol.2016.146654. Epub 2016 May 12.
The role of antiplatelet therapy as primary prophylaxis of thrombosis in low-risk essential thrombocythemia has not been studied in randomized clinical trials. We assessed the benefit/risk of low-dose aspirin in 433 patients with low-risk essential thrombocythemia (271 with a CALR mutation, 162 with a JAK2(V617F) mutation) who were on antiplatelet therapy or observation only. After a follow up of 2215 person-years free from cytoreduction, 25 thrombotic and 17 bleeding episodes were recorded. In CALR-mutated patients, antiplatelet therapy did not affect the risk of thrombosis but was associated with a higher incidence of bleeding (12.9 versus 1.8 episodes per 1000 patient-years, P=0.03). In JAK2(V617F)-mutated patients, low-dose aspirin was associated with a reduced incidence of venous thrombosis with no effect on the risk of bleeding. Coexistence of JAK2(V617F)-mutation and cardiovascular risk factors increased the risk of thrombosis, even after adjusting for treatment with low-dose aspirin (incidence rate ratio: 9.8; 95% confidence interval: 2.3-42.3; P=0.02). Time free from cytoreduction was significantly shorter in CALR-mutated patients with essential thrombocythemia than in JAK2(V617F)-mutated ones (median time 5 years and 9.8 years, respectively; P=0.0002) and cytoreduction was usually necessary to control extreme thrombocytosis. In conclusion, in patients with low-risk, CALR-mutated essential thrombocythemia, low-dose aspirin does not reduce the risk of thrombosis and may increase the risk of bleeding.
抗血小板治疗作为低风险原发性血小板增多症血栓形成一级预防的作用尚未在随机临床试验中进行研究。我们评估了433例低风险原发性血小板增多症患者(271例携带CALR突变,162例携带JAK2(V617F)突变)使用低剂量阿司匹林进行抗血小板治疗或仅观察的获益/风险。在2215人年未进行细胞减灭治疗的随访后,记录到25次血栓形成事件和17次出血事件。在携带CALR突变的患者中,抗血小板治疗不影响血栓形成风险,但与更高的出血发生率相关(每1000患者年12.9次事件与1.8次事件,P=0.03)。在携带JAK2(V617F)突变的患者中,低剂量阿司匹林与静脉血栓形成发生率降低相关,对出血风险无影响。JAK2(V617F)突变与心血管危险因素并存会增加血栓形成风险,即使在调整低剂量阿司匹林治疗后也是如此(发病率比:9.8;95%置信区间:2.3-42.3;P=0.02)。携带CALR突变的原发性血小板增多症患者未进行细胞减灭治疗的时间显著短于携带JAK2(V617F)突变的患者(中位时间分别为5年和9.8年;P=0.0002),通常需要进行细胞减灭治疗以控制极度血小板增多。总之,在低风险、携带CALR突变的原发性血小板增多症患者中,低剂量阿司匹林不能降低血栓形成风险,且可能增加出血风险。