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Acute lymphoid leukemia is a childhood cancer that in high-income countries has event-free survival rates of 80% and global survival rates of 90%. In Brazil these rates are under 70%. This difference may be due to the implementation of supportive care, including the assessment of asparaginase (ASNase) activity. ASNase may cause hypersensitivity reactions and silent drug inactivation. For this reason, ASNase activity monitoring is an essential tool to ensure an effective treatment. Our aim was to implement an ASNase activity measurement technique at a hospital setting. samples from children who were given Escherichia coli-derived ASNase were collected. The results of the analyses conducted in our laboratory Hospital de Clínicas de Porto Alegre were compared to those of two institutions: Centro Infantil Boldrini and University of Munster. 262 samples were assessed. The results of the first analyses were compared with those obtained at Centro Infantil Boldrini and showed an ICC of 0.954. Thirty samples were sent to the University of Munster and presented an ICC was 0.960. Our results, when compared to those of national and international centers, showed an excellent agreement. The study was able to implement an ASNase activity test to monitor the treatment.
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http://dx.doi.org/10.1038/s41598-020-78549-y | DOI Listing |
Int J Biol Macromol
August 2025
Bursa Uludag University, Faculty of Arts and Science, Department of Chemistry, 16059 Gorukle, Bursa, Turkey. Electronic address:
In this study, poly(2-hydroxyethyl methacrylate-N-methacryloyl-(L)-histidine methyl ester-Cu) [PHMCu] nanoparticles were synthesized by emulsion polymerization and used as carriers for L-asparaginase (L-ASNase) immobilization. The nanoparticles were characterized using SEM-EDX, TEM, FTIR, Zeta potential analyses. The binding affinity of L-ASNase on metal-chelated polymeric nanoparticles was investigated via surface plasmon resonance (SPR) analysis.
View Article and Find Full Text PDFInt J Biol Macromol
August 2025
Laboratorio de Catálisis y Biocatálisis, Departamento de Química, Facultad de Ciencias, Universidad de La Serena, Casilla 599, Benavente 980, La Serena 1720236, Chile. Electronic address:
Therapeutic enzymes hold great promise in cancer treatment, yet their clinical application is often limited by instability in physiological environments. This study investigates the application of a silica-chitosan hybrid matrix as a protective and responsive carrier for glucose oxidase (GOx) and asparaginase (ASNase), two enzymes with potential antitumor properties. The encapsulation process was optimized using GOx, achieving an encapsulation efficiency of up to 84.
View Article and Find Full Text PDFEur J Drug Metab Pharmacokinet
August 2025
Department of Paediatric Haematology and Oncology, University Children's Hospital Muenster, Muenster, Germany.
Background And Objectives: Focusing on pharmacokinetic-derived individual dose-intensity parameter values (DIPs), we modeled the pharmacokinetics of polyethylene glycol-conjugated asparaginase (PEG-ASNase) in all treatment phases and different trial groups of AIEOP-BFM ALL 2009.
Methods: Children with acute lymphoblastic leukemia received 1-10 weekly or biweekly repetitive doses (2500 U/m/dose intravenously). A population pharmacokinetic (popPK) model was extended to all phases to describe the pharmacokinetics and the impact of anti-PEG- and anti-asparaginase-antibodies in the German/Czech group (2535 patients, aspartic acid β-hydroxamate (AHA) assay) and validated the model in the Italian group (1603 patients, medac asparaginase activity test (MAAT) assay).
Fundam Clin Pharmacol
October 2025
Science for Life Laboratory (SciLifeLab), Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Background: Cisplatin and its derivatives remain a cornerstone in the treatment of solid malignancies. Resistance is a major factor limiting their clinical utility.
Objectives: In the present study, we set out to interrogate therapeutic approaches to target cisplatin-resistant cancer cells.
J Proteome Res
September 2025
Metabolomics Core Facility, Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, United States.
Poor therapeutic indexes are a principal cause of drug attrition during development. To develop multiomic methods for elucidating potentially targetable mechanisms of drug toxicity, we performed profiling of the response to subtoxic and toxic doses of l-Asparaginase (ASNase) in immune-compromised mice. ASNase is an enzyme-drug approved for the treatment of pediatric acute lymphoblastic leukemia (ALL) but too toxic for use in adults, making it an ideal test case.
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