Distinct clinico-molecular arterial and venous thrombosis scores for myeloproliferative neoplasms risk stratification
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 a...
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creator | Pasquer, Hélène Daltro de Oliveira, Rafael Vasseur, Loic Soret-Dulphy, Juliette Maslah, Nabih Zhao, Lin-Pierre Marcault, Clémence Cazaux, Marine Gauthier, Nicolas Verger, Emmanuelle Parquet, Nathalie Vainchenker, William Raffoux, Emmanuel Ugo, Valérie Luque Paz, Damien Roy, Lydia Lambert, Wayne-Corentin Ianotto, Jean-Christophe Lippert, Eric Giraudier, Stéphane Cassinat, Bruno Kiladjian, Jean-Jacques Benajiba, Lina |
description | 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. |
doi_str_mv | 10.1038/s41375-023-02114-5 |
format | Article |
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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.</description><identifier>ISSN: 0887-6924</identifier><identifier>EISSN: 1476-5551</identifier><identifier>DOI: 10.1038/s41375-023-02114-5</identifier><identifier>PMID: 38148396</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45/23 ; 692/499 ; 692/699/1541/1990/2331 ; Cancer Research ; Cardiovascular diseases ; Critical Care Medicine ; Health risks ; Hematology ; Humans ; Intensive ; Internal Medicine ; Janus Kinase 2 - genetics ; Life Sciences ; Medicine ; Medicine & Public Health ; Middle Aged ; Mutation ; Myeloproliferative Disorders - complications ; Myeloproliferative Disorders - genetics ; Neoplasms ; Neoplasms - complications ; Oncology ; Risk Assessment ; Risk Factors ; Thromboembolism ; Thrombosis ; Thrombosis - complications ; Thrombosis - genetics ; Tumors ; Venous Thrombosis - genetics</subject><ispartof>Leukemia, 2024-02, Vol.38 (2), p.326-339</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to Springer Nature Limited.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-e8f792990b2947f1f0ba259bd78149b71326d06823aadfcefaeb35164d42058b3</citedby><cites>FETCH-LOGICAL-c409t-e8f792990b2947f1f0ba259bd78149b71326d06823aadfcefaeb35164d42058b3</cites><orcidid>0000-0002-4523-675X ; 0000-0001-5440-1115 ; 0000-0001-9074-7287 ; 0000-0002-2312-6584 ; 0000-0002-5553-462X ; 0000-0001-5035-4470 ; 0000-0002-9252-2046 ; 0000-0003-4705-202X ; 0000-0001-9065-0477 ; 0000-0002-6514-3905 ; 0000-0002-1817-2236</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38148396$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04470922$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Pasquer, Hélène</creatorcontrib><creatorcontrib>Daltro de Oliveira, Rafael</creatorcontrib><creatorcontrib>Vasseur, Loic</creatorcontrib><creatorcontrib>Soret-Dulphy, Juliette</creatorcontrib><creatorcontrib>Maslah, Nabih</creatorcontrib><creatorcontrib>Zhao, Lin-Pierre</creatorcontrib><creatorcontrib>Marcault, Clémence</creatorcontrib><creatorcontrib>Cazaux, Marine</creatorcontrib><creatorcontrib>Gauthier, Nicolas</creatorcontrib><creatorcontrib>Verger, Emmanuelle</creatorcontrib><creatorcontrib>Parquet, Nathalie</creatorcontrib><creatorcontrib>Vainchenker, William</creatorcontrib><creatorcontrib>Raffoux, Emmanuel</creatorcontrib><creatorcontrib>Ugo, Valérie</creatorcontrib><creatorcontrib>Luque Paz, Damien</creatorcontrib><creatorcontrib>Roy, Lydia</creatorcontrib><creatorcontrib>Lambert, Wayne-Corentin</creatorcontrib><creatorcontrib>Ianotto, Jean-Christophe</creatorcontrib><creatorcontrib>Lippert, Eric</creatorcontrib><creatorcontrib>Giraudier, Stéphane</creatorcontrib><creatorcontrib>Cassinat, Bruno</creatorcontrib><creatorcontrib>Kiladjian, Jean-Jacques</creatorcontrib><creatorcontrib>Benajiba, Lina</creatorcontrib><title>Distinct clinico-molecular arterial and venous thrombosis scores for myeloproliferative neoplasms risk stratification</title><title>Leukemia</title><addtitle>Leukemia</addtitle><addtitle>Leukemia</addtitle><description>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.</description><subject>45/23</subject><subject>692/499</subject><subject>692/699/1541/1990/2331</subject><subject>Cancer Research</subject><subject>Cardiovascular diseases</subject><subject>Critical Care Medicine</subject><subject>Health risks</subject><subject>Hematology</subject><subject>Humans</subject><subject>Intensive</subject><subject>Internal Medicine</subject><subject>Janus Kinase 2 - genetics</subject><subject>Life Sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Myeloproliferative Disorders - complications</subject><subject>Myeloproliferative Disorders - genetics</subject><subject>Neoplasms</subject><subject>Neoplasms - complications</subject><subject>Oncology</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Thromboembolism</subject><subject>Thrombosis</subject><subject>Thrombosis - 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genetics</topic><topic>Life Sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Myeloproliferative Disorders - complications</topic><topic>Myeloproliferative Disorders - genetics</topic><topic>Neoplasms</topic><topic>Neoplasms - complications</topic><topic>Oncology</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Thromboembolism</topic><topic>Thrombosis</topic><topic>Thrombosis - complications</topic><topic>Thrombosis - genetics</topic><topic>Tumors</topic><topic>Venous Thrombosis - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pasquer, Hélène</creatorcontrib><creatorcontrib>Daltro de Oliveira, Rafael</creatorcontrib><creatorcontrib>Vasseur, Loic</creatorcontrib><creatorcontrib>Soret-Dulphy, Juliette</creatorcontrib><creatorcontrib>Maslah, Nabih</creatorcontrib><creatorcontrib>Zhao, Lin-Pierre</creatorcontrib><creatorcontrib>Marcault, Clémence</creatorcontrib><creatorcontrib>Cazaux, Marine</creatorcontrib><creatorcontrib>Gauthier, Nicolas</creatorcontrib><creatorcontrib>Verger, Emmanuelle</creatorcontrib><creatorcontrib>Parquet, Nathalie</creatorcontrib><creatorcontrib>Vainchenker, William</creatorcontrib><creatorcontrib>Raffoux, Emmanuel</creatorcontrib><creatorcontrib>Ugo, Valérie</creatorcontrib><creatorcontrib>Luque Paz, Damien</creatorcontrib><creatorcontrib>Roy, Lydia</creatorcontrib><creatorcontrib>Lambert, Wayne-Corentin</creatorcontrib><creatorcontrib>Ianotto, Jean-Christophe</creatorcontrib><creatorcontrib>Lippert, Eric</creatorcontrib><creatorcontrib>Giraudier, Stéphane</creatorcontrib><creatorcontrib>Cassinat, Bruno</creatorcontrib><creatorcontrib>Kiladjian, Jean-Jacques</creatorcontrib><creatorcontrib>Benajiba, Lina</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Leukemia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pasquer, Hélène</au><au>Daltro de Oliveira, Rafael</au><au>Vasseur, Loic</au><au>Soret-Dulphy, Juliette</au><au>Maslah, Nabih</au><au>Zhao, Lin-Pierre</au><au>Marcault, Clémence</au><au>Cazaux, Marine</au><au>Gauthier, Nicolas</au><au>Verger, Emmanuelle</au><au>Parquet, Nathalie</au><au>Vainchenker, William</au><au>Raffoux, Emmanuel</au><au>Ugo, Valérie</au><au>Luque Paz, Damien</au><au>Roy, Lydia</au><au>Lambert, Wayne-Corentin</au><au>Ianotto, Jean-Christophe</au><au>Lippert, Eric</au><au>Giraudier, Stéphane</au><au>Cassinat, Bruno</au><au>Kiladjian, Jean-Jacques</au><au>Benajiba, Lina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct clinico-molecular arterial and venous thrombosis scores for myeloproliferative neoplasms risk stratification</atitle><jtitle>Leukemia</jtitle><stitle>Leukemia</stitle><addtitle>Leukemia</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>38</volume><issue>2</issue><spage>326</spage><epage>339</epage><pages>326-339</pages><issn>0887-6924</issn><eissn>1476-5551</eissn><abstract>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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>38148396</pmid><doi>10.1038/s41375-023-02114-5</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-4523-675X</orcidid><orcidid>https://orcid.org/0000-0001-5440-1115</orcidid><orcidid>https://orcid.org/0000-0001-9074-7287</orcidid><orcidid>https://orcid.org/0000-0002-2312-6584</orcidid><orcidid>https://orcid.org/0000-0002-5553-462X</orcidid><orcidid>https://orcid.org/0000-0001-5035-4470</orcidid><orcidid>https://orcid.org/0000-0002-9252-2046</orcidid><orcidid>https://orcid.org/0000-0003-4705-202X</orcidid><orcidid>https://orcid.org/0000-0001-9065-0477</orcidid><orcidid>https://orcid.org/0000-0002-6514-3905</orcidid><orcidid>https://orcid.org/0000-0002-1817-2236</orcidid></addata></record> |
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source | MEDLINE; Alma/SFX Local Collection |
subjects | 45/23 692/499 692/699/1541/1990/2331 Cancer Research Cardiovascular diseases Critical Care Medicine Health risks Hematology Humans Intensive Internal Medicine Janus Kinase 2 - genetics Life Sciences Medicine Medicine & Public Health Middle Aged Mutation Myeloproliferative Disorders - complications Myeloproliferative Disorders - genetics Neoplasms Neoplasms - complications Oncology Risk Assessment Risk Factors Thromboembolism Thrombosis Thrombosis - complications Thrombosis - genetics Tumors Venous Thrombosis - genetics |
title | Distinct clinico-molecular arterial and venous thrombosis scores for myeloproliferative neoplasms risk stratification |
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