Université Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.
INSERM UMR 944, Institut de Recherche Saint-Louis, Paris, France.
Leukemia. 2024 Feb;38(2):326-339. doi: 10.1038/s41375-023-02114-5. Epub 2023 Dec 27.
Current recommended risk scores to predict thrombotic events associated with myeloproliferative neoplasms (MPN) do not discriminate between arterial and venous thrombosis despite their different physiopathology. To define novel stratification systems, we delineated a comprehensive landscape of MPN associated thrombosis across a large long-term follow-up MPN cohort. Prior arterial thrombosis, age >60 years, cardiovascular risk factors and presence of TET2 or DNMT3A mutations were independently associated with arterial thrombosis in multivariable analysis. ARTS, an ARterial Thrombosis Score, based on these four factors, defined low- (0.37% patients-year) and high-risk (1.19% patients-year) patients. ARTS performance was superior to the two-tiered conventional risk stratification in our training cohort, across all MPN subtypes, as well as in two external validation cohorts. Prior venous thrombosis and presence of a JAK2 mutation with a variant allelic frequency ≥50% were independently associated with venous thrombosis. The discrimination potential of VETS, a VEnous Thrombosis Score based on these two factors, was poor, similar to the two-tiered conventional risk stratification. Our study pinpoints arterial and venous thrombosis clinico-molecular differences and proposes an arterial risk score for more accurate patients' stratification. Further improvement of venous risk scores, accounting for additional factors and considering venous thrombosis as a heterogeneous entity is warranted.
目前用于预测与骨髓增殖性肿瘤(MPN)相关血栓事件的风险评分并不能区分动脉血栓和静脉血栓,尽管它们的病理生理学不同。为了定义新的分层系统,我们在一个大型的长期 MPN 队列中描绘了 MPN 相关血栓形成的全面情况。多变量分析显示,先前的动脉血栓形成、年龄>60 岁、心血管危险因素和 TET2 或 DNMT3A 突变的存在与动脉血栓形成独立相关。基于这四个因素的 ARTS(动脉血栓形成评分)定义了低危(0.37%患者年)和高危(1.19%患者年)患者。在我们的训练队列中,以及在两个外部验证队列中,ARTS 在所有 MPN 亚型中的表现均优于两级传统风险分层。先前的静脉血栓形成和 JAK2 突变的存在,其变异等位基因频率≥50%与静脉血栓形成独立相关。基于这两个因素的 VETS(静脉血栓形成评分)的鉴别潜力较差,与两级传统风险分层相似。我们的研究指出了动脉和静脉血栓形成的临床分子差异,并提出了一种动脉风险评分,以更准确地对患者进行分层。需要进一步改进静脉风险评分,考虑到其他因素,并将静脉血栓形成视为一种异质实体。