Distinct clinico-molecular arterial and venous thrombosis scores for myeloproliferative neoplasms risk stratification

被引:10
|
作者
Pasquer, Helene [1 ,2 ]
de Oliveira, Rafael Daltro [1 ]
Vasseur, Loic [1 ]
Soret-Dulphy, Juliette [1 ]
Maslah, Nabih [3 ,4 ]
Zhao, Lin-Pierre [1 ]
Marcault, Clemence [1 ]
Cazaux, Marine [1 ]
Gauthier, Nicolas [1 ]
Verger, Emmanuelle [3 ,4 ]
Parquet, Nathalie [5 ]
Vainchenker, William [6 ]
Raffoux, Emmanuel [5 ]
Ugo, Valerie [7 ]
Luque Paz, Damien [7 ]
Roy, Lydia [8 ]
Lambert, Wayne-Corentin [9 ]
Ianotto, Jean-Christophe [10 ]
Lippert, Eric [9 ]
Giraudier, Stephane [3 ,4 ]
Cassinat, Bruno [3 ,4 ]
Kiladjian, Jean-Jacques [1 ,4 ]
Benajiba, Lina [1 ,2 ]
机构
[1] Univ Paris Cite, Hop St Louis, AP HP, INSERM,Ctr Invest Clin,CIC 1427, Paris, France
[2] Inst Rech St Louis, INSERM, UMR 944, Paris, France
[3] Univ Paris Cite, Hop St Louis, AP HP, Lab Biol Cellulaire, Paris, France
[4] Inst Rech St Louis, INSERM, UMR 1131, Paris, France
[5] Univ Paris Cite, Hop St Louis, AP HP, APHP, Paris, France
[6] Hop St Louis, AP HP, APHP, Paris, France
[7] Nantes Univ, Nantes Universite, CHU Angers, CNRS,Inserm,CRCI2NA, Angers, France
[8] Univ Paris Est Creteil, Hop Henri Mondor, AP HP, Serv Hematol, Creteil, France
[9] Univ Bretagne Occidentale, Serv Hematol Biol, CHU Brest, Brest, France
[10] Univ Bretagne Occidentale, Serv dHematol & dHemostase Clin, Serv Hematol & Hemostase Clin, Brest, France
关键词
JAK2 V617F MUTATION; POLYCYTHEMIA-VERA; ESSENTIAL THROMBOCYTHEMIA; CARDIOVASCULAR-DISEASE; CELL-FUNCTION; SURVIVAL; PATHOPHYSIOLOGY; MYELOFIBROSIS; LEUKOCYTOSIS; MECHANISMS;
D O I
10.1038/s41375-023-02114-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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(V617F) 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.
引用
收藏
页码:326 / 339
页数:14
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