Evidence map›Paper›PMID 39293089›Full record

ArticleBlood advances2024

Risk of bleeding in patients with essential thrombocythemia and extreme thrombocytosis.

Rathnam K Venkat, Robert A Redd, Amyah C Harris, Martin J Aryee, Anna E Marneth, Baransel Kamaz, Chulwoo J Kim, Mohammed Wazir, Lachelle D Weeks, Maximilian Stahl and 5 more

Abstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  5. Review
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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

15 authors.

Rathnam K VenkatDepartment of Medicine, Tufts University School of Medicine, Boston, MA.ORCID 0000-0001-9794-5817
Robert A ReddDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-1329-5288
Amyah C HarrisDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Martin J AryeeDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA.
Anna E MarnethDepartment of Laboratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0001-9065-0581
Baransel KamazDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Boston, MA.ORCID 0000-0002-9910-6141
Chulwoo J KimDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Boston, MA.
Mohammed WazirDivision of Hematology-Oncology, UMass Chan Medical School, Worcester, MA.
Lachelle D WeeksDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-8726-6212
Maximilian StahlDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Daniel J DeAngeloDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-7865-2306
R Coleman LindsleyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-9822-806X
Marlise R LuskinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-5781-4529
Gabriela S HobbsDivision of Hematology/Oncology, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-0199-9333
Joan HowDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-6421-0117

Funding

Single Cell and ImmunogenomicsP01CA229092 · NCI · DANA-FARBER CANCER INST · PI RITZ, JEROME · 2019 to 2023
$13.8M
NCI NIH HHS P01 CA229092
6 · The paper itself

Abstract

abstractApproximately 25% of patients with essential thrombocythemia (ET) present with extreme thrombocytosis (ExT), defined as having a platelet count ≥1000 × 109/L. ExT patients may have an increased bleeding risk associated with acquired von Willebrand syndrome. We retrospectively analyzed the risk of bleeding and thrombosis in ExT vs non-ExT patients with ET at Dana-Farber Cancer Institute and Massachusetts General Hospital from 2014 to 2022 to inform treatment decisions. We abstracted the first major bleed, clinically relevant nonmajor bleed (CRNMB), and thrombotic events from medical records. We identified 128 ExT patients (28%) and 323 non-ExT patients (72%). Cumulative incidence of bleeding was not different in ExT vs non-ExT patients (21% vs 13% [P = .28] for major bleed; 16% vs 15% [P = .50] for CRNMB). Very low and low thrombotic risk ExT patients were more likely to be cytoreduced than very low- and low-risk non-ExT patients (69% vs 50% [P = .060] for very low risk; 83% vs 53% [P = .0059] for low risk). However, we found no differences in bleeding between ExT and non-ExT patients when restricting the risk of bleed from diagnosis to cytoreduction start date (28% vs 19% [P = .29] for major bleed; 24% vs 22% [P = .75] for CRNMB). Cumulative incidence of thrombosis was also not different between ExT and non-ExT patients (28% vs 25%; P = .98). This suggests that cytoreduction may not be necessary to reduce bleeding risk based only on a platelet count of 1 million. We identified novel risk factors for bleeding in patients with ET including diabetes mellitus and the DNMT3A mutation.

Indexed as

HemorrhageThrombocythemia, EssentialThrombocytosisAdultAgedFemaleHumansIncidenceMaleMiddle AgedPlatelet CountRetrospective StudiesRisk FactorsThrombosis

Identifiers

PMID39293089
PMCPMC11635702

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.