Evidence map›Paper›PMID 41170879›Full record

ArticleBlood advances2026

Derivation and external validation of a venous thromboembolism risk prediction model in asparaginase-treated ALL.

Daniela R Anderson, Radhika Gangaraju, Wafik George Sedhom, Eva N Hamulyák, Tzu-Fei Wang, Kristin O'Dwyer, Brian J Carney, Chandrasekar Muthiah, Michaela Liedtke, Talha Badar and 25 more

Abstract readMulticenter StudyValidation Study
In one paragraph

Article in Blood advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

35 authors.

Daniela R AndersonDepartment of Family Medicine, University of Chicago, Chicago, IL.
Radhika GangarajuDivision of Hematology-Oncology, Institute for Cancer Outcomes and Survivorship, The University of Alabama at Birmingham, Birmingham, AL.
Wafik George SedhomDepartment of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL.
Eva N HamulyákDepartment of Hematology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-9340-8771
Tzu-Fei WangDepartment of Medicine, University of Ottawa at The Ottawa Hospital and Ottawa Hospital Research Institute, Ottawa, ON, Canada.ORCID 0000-0003-2407-9000
Kristin O'DwyerDepartment of Medicine, Wilmot Cancer Institute of University of Rochester, Rochester, NY.ORCID 0000-0001-8517-8198
Brian J CarneyDivision of Hematology and Hematologic Malignancies, Beth Israel Deaconess Medical Center, Boston, MA.
Chandrasekar MuthiahDivision of Hematology-Oncology, Medical College of Wisconsin, Milwaukee, WI.
Michaela LiedtkeDivision of Hematology, Department of Medicine, Stanford Health Care, Stanford, CA.ORCID 0000-0001-8945-5850
Talha BadarDivision of Hematology, Mayo Clinic, Jacksonville, FL.ORCID 0000-0003-1548-918X
Shai ShimonyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-7245-9652
Renana RobinsonInstitute of Hematology, Department of Medicine, Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.ORCID 0000-0003-0239-9265
Kristen SanfilippoDivision of Hematology, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-0433-7845
Andriy DerkachDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-2178-8493
Shira DinnerDepartment of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL.
Bart J BiemondDepartment of Hematology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-4426-5743
David NemirovskyDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.
Leah A GoldbergDepartment of Internal Medicine, University of Chicago Medical Center, Chicago, IL.
Anjani D KapadiaDepartment of Internal Medicine and Pediatrics, University of Chicago Medical Center, Chicago, IL.
Hannah LevaviDepartment of Medicine, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.ORCID 0000-0003-4912-2992
Michal Bar-NatanDivision of Hematology and Medical Oncology at New York-Presbyterian Hospital/Weill Cornell Medical Center, New York, NY.
Grace Van HyfteDepartment of Population Health Science and Policy and Institute for Healthcare Delivery Science, Icahn School of Medicine at Mount Sinai, New York, NY.
Karan BansalDivision of Hematology-Oncology, Institute for Cancer Outcomes and Survivorship, The University of Alabama at Birmingham, Birmingham, AL.
Marc CarrierDepartment of Medicine, University of Ottawa at The Ottawa Hospital and Ottawa Hospital Research Institute, Ottawa, ON, Canada.ORCID 0000-0001-8296-2972
Jill FulcherDepartment of Medicine, University of Ottawa at The Ottawa Hospital and Ottawa Hospital Research Institute, Ottawa, ON, Canada.ORCID 0000-0002-0369-5034
Anke M GerritsDepartment of Internal Medicine, OLVG, Amsterdam, The Netherlands.
Mark R LitzowDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.ORCID 0000-0002-9816-6302
Selina LugerDivision of Hematology/Oncology and Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
Guru Subramanian Guru MurthyDivision of Hematology-Oncology, Medical College of Wisconsin, Milwaukee, WI.
Marlise LuskinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-5781-4529
Ofir WolachInstitute of Hematology, Department of Medicine, Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.ORCID 0000-0002-8662-0707
William ShomaliDepartment of Medicine, Stanford University School of Medicine/Stanford Cancer Institute, Stanford, CA.ORCID 0000-0001-6500-350X
Jeffrey I ZwickerHematology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-5810-6893
Wendy StockSection of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL.
Avi LeaderHematology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Clonal Hematopoiesis in a Biracial PopulationK08HL159290 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Radhika Gangaraju · 2022 to 2026
$820k
NCI NIH HHS P30 CA008748NHLBI NIH HHS K08 HL159290
6 · The paper itself

Abstract

abstractThe incidence of venous thromboembolism (VTE) in patients with acute lymphoblastic leukemia (ALL) receiving asparaginase-based induction is high despite primary thromboprophylaxis. Our aim was to derive and externally validate a VTE risk prediction model in patients with ALL receiving asparaginase-based induction. We conducted a multicenter retrospective cohort study of patients (aged ≥18 years) with newly diagnosed ALL receiving asparaginase-based induction. The derivation and external validation cohorts included 306 and 94 patients, respectively. Primary outcome was VTE at any site. A cause-specific Cox proportional hazards model stratified by thromboprophylaxis and center was performed to identify VTE risk factors in the derivation cohort. A risk prediction model for VTE at 30 days was derived using variables with P value < .05 in the multivariable model and was tested in the validation cohort. VTE risk factors on multivariable analysis in the derivation cohort included D-dimer ≥1 μg fibrinogen equivalent unit per mL (hazard ratio [HR], 2.64; 95% confidence interval [CI], 1.07-6.5) and hemoglobin (HR for each 1 g/dL increment, 1.19; 95% CI, 1.06-1.34) at ALL diagnosis. A VTE risk score based on these variables distinguished between a 4% (95% CI, 0.72-12) and 20% (95% CI, 14-27) 30-day cumulative incidence of VTE in the derivation cohort, with similar findings in the validation cohort (area under the curve, 0.56). The negative predictive value for VTE at 30 days was 96% and 93% in the derivation and validation cohorts, respectively, and the positive predictive value was 20% in both. We derived and validated a model using D-dimer and hemoglobin, which stratifies VTE risk in patients with ALL receiving asparaginase-based induction.

Indexed as

AsparaginasePrecursor Cell Lymphoblastic Leukemia-LymphomaVenous ThromboembolismAdolescentAdultFemaleHumansIncidenceMaleMiddle AgedProportional Hazards ModelsRetrospective StudiesRisk AssessmentRisk FactorsYoung AdultAsparaginase

Identifiers

PMID41170879
PMCPMC12865561

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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.