» Articles » PMID: 31030032

Risk Factors for Symptomatic Venous Thromboembolism During Therapy for Childhood Acute Lymphoblastic Leukemia

Overview
Journal Thromb Res
Date 2019 Apr 29
PMID 31030032
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Symptomatic venous thromboembolism (VTE) is an unpredictable and life-threatening toxicity, which occurs early in childhood acute lymphoblastic leukemia (ALL) therapy. Approximately 5% of children will experience VTE which is treated with anticoagulation. Asparaginase and corticosteroids are etiologic factors for VTE, however other clinical factors may modify this risk.

Procedure: We sought to i) assess published pre-treatment VTE risk factors ii) identify early clinical factors that were associated with VTE and iii) determine whether single nucleotide polymorphisms (SNPs) associated with VTE in non-cancer patients contributed to VTE in children with ALL. We performed a detailed, retrospective analysis of 1021 ALL patients treated between 1998 and 2013. Individual patient records were reviewed to ascertain VTE incidence and document treatment-related clinical variables.

Results: The incidence of VTE was 5.1%. Extremes of weight at diagnosis (<5th or >95th centile) was an independent risk factor in multivariable analysis, when added to published risk factors of age ≥10 years and mediastinal mass. When factors during induction/consolidation were considered separately: bacteremia, elevated serum gamma-glutamyl transferase and bilirubin were associated with VTE occurrence. None of the SNPs associated with VTE in non-cancer populations were significantly associated with VTE in our cohort.

Conclusion: We found two known risk factors (age ≥ 10 years and mediastinal mass) in a large cohort of children treated for ALL and identified other factors associated with VTE such as weight extremes at diagnosis, bacteremia, and abnormal liver function which warrant further study. These VTE risk factors may form the basis of future thromboprophylaxis trials.

Citing Articles

Prospective longitudinal evaluation of treatment-related toxicity and health-related quality of life during the first year of treatment for pediatric acute lymphoblastic leukemia.

Schilstra C, McCleary K, Fardell J, Donoghoe M, McCormack E, Kotecha R BMC Cancer. 2022; 22(1):985.

PMID: 36109702 PMC: 9479356. DOI: 10.1186/s12885-022-10072-x.


Cerebral sinuses thrombosis prior to the diagnosis of acute lymphoblastic leukemia in a child: A case report.

Sherief L, Zakaria M, Soliman B, Kamal N, Alharthi S, Abosabie S SAGE Open Med Case Rep. 2022; 10:2050313X221117337.

PMID: 35991951 PMC: 9382063. DOI: 10.1177/2050313X221117337.


Clinical and demographic factors contributing to asparaginase-associated toxicities in children with acute lymphoblastic leukemia.

Dharia P, Swartz M, Bernhardt M, Chen H, Gramatges M, Lupo P Leuk Lymphoma. 2022; 63(12):2948-2954.

PMID: 35895075 PMC: 9745725. DOI: 10.1080/10428194.2022.2102621.


Acute central nervous system toxicity during treatment of pediatric acute lymphoblastic leukemia: phenotypes, risk factors and genotypes.

Anastasopoulou S, Nielsen R, Als-Nielsen B, Banerjee J, Eriksson M, Helenius M Haematologica. 2022; 107(10):2318-2328.

PMID: 35354251 PMC: 9521239. DOI: 10.3324/haematol.2021.280016.


Asparaginase enzyme activity levels and toxicity in childhood acute lymphoblastic leukemia: a NOPHO ALL2008 study.

Stensig Lynggaard L, Rank C, Hansen S, Hojfeldt S, Henriksen L, Brunsvig Jarvis K Blood Adv. 2021; 6(1):138-147.

PMID: 34625787 PMC: 8753199. DOI: 10.1182/bloodadvances.2021005631.