Evidence map›Paper›PMID 38148396›Full record

ArticleLeukemia2024

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

Hélène Pasquer, Rafael Daltro de Oliveira, Loic Vasseur, Juliette Soret-Dulphy, Nabih Maslah, Lin-Pierre Zhao, Clémence Marcault, Marine Cazaux, Nicolas Gauthier, Emmanuelle Verger and 13 more

Abstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Polycythaemia vera.Nature reviews. Disease primers · 2025
    Review
  15. Article
  16. Review
  17. Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Hélène PasquerUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.
Rafael Daltro de OliveiraUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.ORCID http://orcid.org/0000-0002-9252-2046
Loic VasseurUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.ORCID http://orcid.org/0000-0001-9065-0477
Juliette Soret-DulphyUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.
Nabih MaslahUniversité Paris Cité, APHP, Hôpital Saint-Louis, Laboratoire de Biologie Cellulaire, Paris, France.ORCID http://orcid.org/0000-0002-5553-462X
Lin-Pierre ZhaoUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.ORCID http://orcid.org/0000-0001-5035-4470
Clémence MarcaultUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.
Marine CazauxUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.
Nicolas GauthierUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.
Emmanuelle VergerUniversité Paris Cité, APHP, Hôpital Saint-Louis, Laboratoire de Biologie Cellulaire, Paris, France.
Nathalie ParquetUniversité Paris Cité, APHP, Hôpital Saint-Louis, Département d'hématologie et d'Immunologie, Paris, France.
William VainchenkerAPHP, Hôpital Saint-Louis, Département d'hématologie et d'Immunologie, Paris, France.ORCID http://orcid.org/0000-0003-4705-202X
Emmanuel RaffouxUniversité Paris Cité, APHP, Hôpital Saint-Louis, Département d'hématologie et d'Immunologie, Paris, France.
Valérie UgoUniv Angers, Nantes Université, CHU Angers, Inserm, CNRS, CRCI2NA, Angers, France.
Damien Luque PazUniv Angers, Nantes Université, CHU Angers, Inserm, CNRS, CRCI2NA, Angers, France.ORCID http://orcid.org/0000-0002-4523-675X
Lydia RoyUniversité Paris Est Créteil, APHP, Hôpital Henri Mondor, Service d'hématologie, Créteil, France.
Wayne-Corentin LambertUniversité de Bretagne Occidentale, CHU de Brest, Service d'Hématologie Biologique, Brest, France.
Jean-Christophe IanottoUniversité de Bretagne Occidentale, CHU de Brest, Service d'Hématologie et d'Hémostase Clinique, Brest, France.ORCID http://orcid.org/0000-0001-9074-7287
Eric LippertUniversité de Bretagne Occidentale, CHU de Brest, Service d'Hématologie Biologique, Brest, France.ORCID http://orcid.org/0000-0002-2312-6584
Stéphane GiraudierUniversité Paris Cité, APHP, Hôpital Saint-Louis, Laboratoire de Biologie Cellulaire, Paris, France.ORCID http://orcid.org/0000-0002-1817-2236
Bruno CassinatUniversité Paris Cité, APHP, Hôpital Saint-Louis, Laboratoire de Biologie Cellulaire, Paris, France.ORCID http://orcid.org/0000-0002-6514-3905
Jean-Jacques KiladjianUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France.
Lina BenajibaUniversité Paris Cité, APHP, Hôpital Saint-Louis, Centre d'Investigations Cliniques, INSERM CIC 1427, Paris, France. lina.benajiba@aphp.fr.ORCID http://orcid.org/0000-0001-5440-1115

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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

Indexed as

Myeloproliferative DisordersNeoplasmsThrombosisVenous ThrombosisHumansJanus Kinase 2Middle AgedMutationRisk AssessmentRisk FactorsJanus Kinase 2

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.