Stefan Nygaard Hansen

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

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  • Line Stensig Lynggaard
  • Cecilie Utke Rank, University of Copenhagen
  • ,
  • Stefan Nygaard Hansen
  • Sofie Gottschalk Højfeldt
  • ,
  • Louise Tram Henriksen
  • Kirsten Brunsvig Jarvis, University of Oslo
  • ,
  • Susanna Ranta, Karolinska Institutet
  • ,
  • Riitta Niinimäki, University of Oulu
  • ,
  • Arja Harila-Saari, Uppsala University
  • ,
  • Benjamin O Wolthers, University of Copenhagen
  • ,
  • Thomas L Frandsen, University of Copenhagen
  • ,
  • Mats Heyman, Karolinska Institutet
  • ,
  • Kjeld Schmiegelow, University of Copenhagen
  • ,
  • Birgitte Klug Albertsen

Asparaginase treatment is a mainstay in contemporary treatment of acute lymphoblastic leukemia (ALL), but substantial asparaginase-related toxicity may lead to jeopardized protocol compliance and compromises survival. We investigated the association between risk of asparaginase-associated toxicities (AspTox) and asparaginase enzyme activity (AEA) levels in 1155 children aged 1.0 to 17.9 years, diagnosed with ALL between July 2008 and March 2016, and treated according to the Nordic Society of Pediatric Hematology and Oncology (NOPHO) ALL2008 protocol. Patients with ≥2 blood samples for AEA measurement drawn 14 ± 2 days after asparaginase administration were included (6944 trough values). AEA was measurable (or >0 IU/L) in 955 patients, whereas 200 patients (17.3%) had asparaginase inactivation and few AspTox recorded. A time-dependent multiple Cox model of time to any first asparaginase-associated toxicity adjusted for sex and age was used. For patients with measurable AEA, we found a hazard ratio (HR) of 1.17 per 100 IU/L increase in median AEA (95% confidence interval [CI], 0.98-1.41; P = .09). For pancreatitis, thromboembolism, and osteonecrosis, the HRs were 1.40 (95% CI, 1.12-1.75; P = .002), 0.99 (95% CI, 0.70-1.40; P = .96), and 1.36 (95% CI, 1.04-1.77; P = .02) per 100 IU/L increase in median AEA, respectively. No significant decrease in the risk of leukemic relapse was found: HR 0.88 per 100 IU/L increase in AEA (95% CI, 0.66-1.16; P = .35). In conclusion, these results emphasize that overall AspTox and relapse are not associated with AEA levels, yet the risk of pancreatitis and osteonecrosis increases with increasing AEA levels.

Original languageEnglish
JournalBlood Advances
Volume6
Issue1
Pages (from-to)138-147
Number of pages10
ISSN2473-9529
DOIs
Publication statusPublished - Jan 2022

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