Evidence map›Paper›PMID 40765905›Full record

ArticleBlood vessels, thrombosis & hemostasis2025

Real-world analysis of strategies to prevent thrombosis and bleeding in adults with ALL treated with asparaginase.

Joseph F Mort, David Brighton, Benjamin Mautner, Eric Pierce, Farid Ghamsari, Cecily Allen, Darren D'Souza, Imari Patel, Justin Lawson, Clayton Jackson and 15 more

Abstract read
In one paragraph

Article in Blood vessels, thrombosis & hemostasis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Risk Assessment for Venous Thrombosis in Lymphoma and Emerging Biomarkers.International journal of molecular sciences · 2026
    Review
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

25 authors.

Joseph F MortDivision of Hematology and Oncology, Department of Medicine, University of Virginia, Charlottesville, VA.
David BrightonDepartment of Public Health Sciences, University of Virginia, Charlottesville, VA.
Benjamin MautnerDivision of Hematology and Oncology, Department of Medicine, University of Virginia, Charlottesville, VA.
Eric PierceDivision of Hematology and Oncology, Department of Medicine, University of Virginia, Charlottesville, VA.
Farid GhamsariDivision of Hematology and Oncology, Department of Medicine, University of Virginia, Charlottesville, VA.
Cecily AllenSection of Hematology, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.
Darren D'SouzaDivision of Hematology and Oncology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD.
Imari PatelDivision of Hematology and Oncology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD.
Justin LawsonDivision of Hematology and Oncology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD.
Clayton JacksonSection of Hematology and Oncology, Department of Internal Medicine, Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC.
Karin AbernathyDepartment of Pharmaceutical Services, Vanderbilt University Medical Center, Nashville, TN.
Bradley YelvingtonDepartment of Pharmaceutical Services, Vanderbilt University Medical Center, Nashville, TN.
Ryan MillerDepartment of Pharmaceutical Services, Vanderbilt University Medical Center, Nashville, TN.
Bhagirathbhai DholariaDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Heather WolfeDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University School of Medicine, Durham, NC.
Jordan InfieldDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University School of Medicine, Durham, NC.
Susan C LockeDuke Cancer Institute, Durham, NC.
Rory M ShallisSection of Hematology, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.
Vu H DuongDivision of Hematology and Oncology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD.
Daniel R ReedSection of Hematology and Oncology, Department of Internal Medicine, Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC.
Katherine WalshDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Thomas W LeBlancDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University School of Medicine, Durham, NC.
Michael KengDivision of Hematology and Oncology, Department of Medicine, University of Virginia, Charlottesville, VA.
Bethany HortonDepartment of Public Health Sciences, University of Virginia, Charlottesville, VA.
Firas El ChaerDivision of Hematology and Oncology, Department of Medicine, University of Virginia, Charlottesville, VA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of adult patients with acute lymphoblastic leukemia (ALL) has improved with the incorporation of pediatric-inspired regimens that contain PEGylated asparaginase (PEG-Asp). However, PEG-Asp administration is associated with an increased rate of thrombosis. Data regarding the benefits of antithrombin (AT) repletion and prophylactic anticoagulation in adults receiving PEG-Asp-based regimens are limited. We performed a retrospective study to evaluate the rates of induction thrombosis and bleeding among adults receiving ALL therapy containing Asp at 6 academic centers in the United States. Of 233 patients who met the inclusion criteria, 98.3% received PEG-Asp. Ninety-six patients (41.2%) had their AT levels monitored, 58 patients (24.9%) received AT repletion, and 41 patients (17.6%) received prophylactic anticoagulation. Thirty-two patients (13.7%) experienced thrombotic events, with half (53.1%) being line-associated thromboses. In multivariate analysis, the odds of thrombosis did not differ between patients who received AT monitoring, AT repletion, or prophylactic anticoagulation. The odds of thrombosis were 4 times higher for patients with peripherally inserted central catheters than for those with other types of central lines (odds ratio, 4.112; 95% confidence interval, 1.622-10.427;

Identifiers

PMID40765905
PMCPMC12320406

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Registered trials

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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.