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April 28, 2026Leukemia & lymphoma/Leukemia and lymphoma1 citationsOpen Access

Asparaginase activity levels and toxicity in children and adolescents with acute lymphoblastic leukemia

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MPMarie‐Claude Pelland‐MarcotteCentre hospitalier universitaire de QuébecCÉChantal ÉthierCentre hospitalier universitaire de QuébecAMAlexis ManirakizaCentre Hospitalier Universitaire Sainte-Justine

Key Points

  • The aim is to determine whether serum asparaginase activity levels correlate with toxicities in children and adolescents with acute lymphoblastic leukemia.
  • Included 84 patients with newly diagnosed acute lymphoblastic leukemia who received at least one dose of asparaginase
  • Measured serum asparaginase activity levels before and after treatment
  • Assessed associations between asparaginase activity and occurrences of thrombosis, pancreatitis, and hypersensitivity events.
  • Median peak SAA level was 2.36 IU/mL and trough level was 0.77 IU/mL
  • High peak SAA levels showed a trend toward increased venous thrombosis risk (HR: 1.51, p = 0.058)
  • No significant association found between SAA levels and acute pancreatitis or hypersensitivity events.

Abstract

Asparaginase (ASP) is a critical treatment component of acute lymphoblastic leukemia (ALL), yet associated with potentially severe complications. We assessed whether serum asparaginase activity (SAA) is associated with development of venous thrombosis, acute pancreatitis, bleeding and/or hypersensitivity events. We included 84 patients (median age 6.4 years, 66% male) with newly diagnosed ALL/lymphoblastic lymphoma who received ≥1 dose of ASP and with ≥1 available SAA level(s). Median peak and trough SAA levels were 2.36 IU/mL and 0.77 IU/mL. High peak SAA levels were associated with a trend toward increased venous thrombosis risk (HR: 1.51, p = 0.058). No association between SAA peak and/or trough levels and acute pancreatitis nor hypersensitivity was observed. SAA do not appear to predict the risk of ASP-related toxicities. Our data do not support individualized dosing to prevent toxicities such as thrombosis or pancreatitis. Larger prospective studies are required to help identify children at high risk of ASP-related toxicities.

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Cite This Study

Pelland‐Marcotte et al. (2026) studied this question.

synapsesocial.com/papers/69f04e08727298f751e72058https://doi.org/10.1080/10428194.2026.2656726
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