Pegaspargase in clinical practice: a literature review and toxicity analysis after 1.5 years of its use in patients with acute lymphoblastic leukemia treated at an oncology/hematology department
- Authors: Boychenko E.G.1, Islamova A.R.1, Senova D.K.1, Garbuzova I.A.1, Prudnikova M.A.1, Filatova N.А.1, Usmanskaya E.E.1, Ivanov N.N.1, Gogun A.A.1, Pshenichnaya K.I.1
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Affiliations:
- Children’s Multi-Specialty Clinical Center of High Medical Technologies
- Issue: Vol 24, No 1 (2025)
- Pages: 88-105
- Section: ORIGINAL ARTICLES
- Submitted: 23.01.2025
- Accepted: 04.02.2025
- Published: 08.07.2025
- URL: https://hemoncim.com/jour/article/view/946
- DOI: https://doi.org/10.24287/1726-1708-2025-24-1-88-105
- ID: 946
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Abstract
Acute lymphoblastic leukemia (ALL) comprises a heterogeneous group of hematological malignancies accounting for approximately 25% of all cancer cases in children under 15 years of age. Over the past 40 years, the treatment of ALL in children has improved drastically due to the development and continuous improvement of risk stratification and incorporation of multiagent chemotherapy protocols including central nervous system prophylaxis. Asparaginase has played a major role in the improvement of ALL treatment outcomes in children and has been a critical part of ALL management since 1960s. L-asparaginase derived from Escherichia coli and Erwinia chrysanthemi is an enzyme causing depletion of serum asparagine which leads to its deprivation and consequent inhibition of protein synthesis, and hence limited survival of lymphoblasts that are known to be highly dependent on exogenous asparagine. Pegaspargase, a conjugate of methoxypolyethylene glycol and L-asparaginase, has become an integral part of treatment protocols for primary and relapsed ALL due to its longer half-life and an improved immunogenicity profile compared to native asparaginase medicines. However, the use of pegaspargase is associated with various toxicity and side effects that are observed in 25–30% of patients, with hypersensitivity being the most common reaction. Other toxicities include asparaginase-associated pancreatitis, thrombosis/bleeding, liver dysfunction, osteonecrosis, and dyslipidemia. Failure to receive the entire course of asparaginase therapy is associated with poorer treatment outcomes. The awareness and rapid identification of asparaginase-associated toxicity ensure effective toxicity prevention and treatment and help achieve maximum benefit from asparaginase therapy. Here, we offer an overview of the most common toxicities associated with pegaspargase treatment based both on literature data and on the results of our analysis of the drug’s clinical use at a Russian pediatric oncology/hematology department. The study was approved by the Independent Ethics Committee of the Children’s Multi-Specialty Clinical Center of High Medical Technologies.
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About the authors
E. G. Boychenko
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Email: boychenko-elmira@yandex.ru
ORCID iD: 0000-0002-2731-4531
Elmira G. Boychenko - Dr. Med. Sci., Head of the Department of Oncology/hematology at Children’s Multi-Specialty Clinical Center of High Medical Technologies, Chief External Expert in Pediatric Hematology of Saint Petersburg Healthcare Committee.
14A Avangardnaya St., 198205 Saint-Petersburg
Russian FederationA. R. Islamova
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Email: alsushka99@bk.ru
ORCID iD: 0009-0003-2794-5514
Saint-Petersburg
Russian FederationD. Kh. Senova
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Author for correspondence.
Email: disanasenova@mail.ru
ORCID iD: 0009-0006-8127-3159
Saint-Petersburg
Russian FederationI. A. Garbuzova
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Saint-Petersburg
Russian FederationM. A. Prudnikova
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Saint-Petersburg
Russian FederationN. А. Filatova
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Saint-Petersburg
Russian FederationE. E. Usmanskaya
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Saint-Petersburg
Russian FederationN. N. Ivanov
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Saint-Petersburg
Russian FederationA. A. Gogun
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Saint-Petersburg
Russian FederationK. I. Pshenichnaya
Children’s Multi-Specialty Clinical Center of High Medical Technologies
Saint-Petersburg
Russian FederationReferences
- Litvinov D.V., Karelin A.F., Romanova K.I., Rumyantseva Yu.V., Karatchunsky A.I. Childhood Acute Lymphoblastic Leukemia Treatment: Current Options and Unsolved Problems. Doctor.Ru 2015; 111 (10): 30–7. (In Russ.)
- Hijiya N., van der Sluis I.M. Asparaginase-associated toxicity in children with acute lymphoblastic leukemia. Leuk Lymphoma 2016; 57 (4): 748–57. doi: 10.3109/10428194.2015.1101098
- Korkina Yu.S., Valiev T.T. Asparaginase drugs: a new view of the mechanism of action, side effects and experience in BFM (Berlin– Frankfurt–Munster) protocols. Russian Journal of Pediatric Hematology and Oncology 2021; 8 (4): 81–9. (In Russ.) doi: 10.21682/2311-1267-2021-8-4-8189
- Smirnova D.S., Valiev T.T. The efficacy and toxicity of L-asparaginase in the treatment of acute lymphoblastic leukemia in children. Pediatric Hematology/ Oncology and Immunopathology 2023; 22 (3): 192–8. (In Russ.) doi: 10.24287/1726-17082023-22-3-192-198
- Valiev T. T. Toxicity of L-asparaginase drugs in acute lymphoblastic leukemia treatment. Oncohematology 2023; 18 (3): 134–9. (In Russ.) doi: 10.17650/1818‐8346‐2023‐18‐3‐134‐139
- Popa A.V. Asparaginase medicines in the treatment of children with acute lymphoblastic leukemia. Effective drug therapy. Oncology, hematology and radiology 2010; 3: 32–5. (In Russ.)
- Alexandrova S.S., Gladilina Yu.A., Pokrovskaya M.V., Sokolov N.N., Zhdanov D.D. Mechanisms of Development of Side Effects and Drug Resistance to Asparaginase and Ways to Overcome Them. Biomedical Chemistry 2022; 68 (2): 104–16. (In Russ.) doi: 10.18097/PBMC20226802104
- Borsakova D.V., Sinauridze E.I. L-asparaginase: new approaches to improve pharmacological characteristics. Pediatric Hematology/Oncology and Immunopathology 2018; 17 (4): 82–99. (In Russ.) doi: 10.24287/1726-1708-2018-17-482-99
- Dolowy W.C., Henson D., Cornet J., Sellin H. Toxic and antineoplastic effects of L-asparaginase. Study of mice with lymphoma and normal monkeys and report on a child with leukemia. Cancer 1966; 19 (12): 1813–9. doi: 10.1002/10970142(196612)19:12<1813::aid-cncr2820191208>3.0.co;2-e
- Hill J.M., Roberts J., Loeb E., Khan A.,MacLellan A., Hill R.W. L-asparaginase therapy for leukemia and other malignant neoplasms. Remission in human leukemia. JAMA 1967; 202 (9): 882–8.
- Egler R.A., Ahuja S.P., Matloub Y. L-asparaginase in the treatment of patients with acute lymphoblastic leukemia. J Pharmacol Pharmacother 2016; 7 (2): 62–71. doi: 10.4103/0976-500X.184769
- Heo Y.A., Syed Y.Y., Keam S.J. Pegaspargase: A Review in Acute Lymphoblastic Leukaemia. Drugs 2019; 79 (7): 767–77. doi: 10.1007/s40265-019-01120-1. Erratum in: Drugs 2019; 79 (8): 901. doi: 10.1007/s40265-019-01137-6
- Bender С., Maese L., CarterFebres M., Verma A. Clinical Utility of Pegaspargase in children, adolescents and young adult patients with acute lymphoblastic leukemia: a review. Blood and Lymphatic Cancer: Targets and Therapy 2021; (11): 25–40. doi: 10.2147/BLCTT.S245210
- Müller H.J., Löning L., Horn A., Schwabe D., Gunkel M., Schrappe M., et al. Pegylated asparaginase (Oncaspar) in children with ALL: drug monitoring in reinduction according to the ALL/NHL-BFM 95 protocols. Br J Haematol 2000; 110 (2): 379–84. doi: 10.1046/j.1365-2141.2000.02187.x
- Avxentyev N.A., Frolov M.Yu., Makarov A.S., Novichkova G.A., Karachunskiy A.I., Rumyantseva Yu.V., et al. A pharmacoeconomic study of pegaspargase in the treatment of pediatric acute lymphoblastic leukemia in Russia. Pediatric Hematology/Oncology and Immunopathology 2022; 21 (4): 60–9. (In Russ.) doi: 10.24287/1726-1708-2022-21-4-60-69
- ALL-MB-2008 clinical study report (version 1.0). M.: The D. Rogachev NMRCPHOI of Ministry of Healthcare of Russia; 2021. (In Russ.)
- The ALL-MB 2015 protocol (version as of 10.10.2015). M.: The D. Rogachev NMRCPHOI of Ministry of Healthcare of Russia; 2015. (In Russ.)
- A.M. Popov. Minimal residual disease detection by immunophenotyping for treatment optimization in children with B cell acute lymphoblastic leukemia. Diss. … of Dr. Med. Sci. М.; 2024. (In Russ.)
- Lopez-Santillan M., Iparraguirre L., Martin-Guerrero I., Gutierrez-Camino A., Garcia-Orad A. Review of pharmacogenetics studies of L-asparaginase hypersensitivity in acute lymphoblastic leukemia points to variants in the GRIA1 gene. Drug Metab Pers Ther 2017; 32 (1): 1–9. doi: 10.1515/dmpt-20160033
- Awwad S., Abu Alnasr R., Almanjomi F., Al Sultan M., Howaidi J., Almotairi M., Al Fayyad I. Peg-asparaginase associated toxicities in children with acute lymphoblastic leukemia: A single-center cross-sectional study. Pediatr Hematol Oncol J 2024; 9: 54–62. doi: 10.1016/j.phoj.2024.03.001
- Van Trimpont M., Peeters E.,De Visser Y., Schalk A.M., Mondelaers V., De Moerloose B., et al. Novel Insights on the Use of L-Asparaginase as an Efficient and Safe Anti-Cancer Therapy. Cancers (Basel) 2022; 14 (4): 902. doi: 10.3390/cancers14040902
- Asselin B., Rizzari C. Asparaginase pharmacokinetics and implications of therapeutic drug monitoring. Leuk Lymphoma 2015; 56 (8): 2273– 80. doi: 10.3109/10428194.2014.100305
- Van der Sluis I.M., Vrooman L.M., Pieters R., Baruchel A., Escherich G., Goulden N., еt аl. Consensus expert recommendations for identification and management of asparaginase hypersensitivity and silent inactivation. Haematologica 2016; 101 (3): 279–85. doi: 10.3324/haematol.2015.137380
- Burke M.J., Zalewska-Szewczyk B. Hypersensitivity reactions to asparaginase therapy in acute lymphoblastic leukemia: immunology and clinical consequences. Future Oncol 2022; 18 (10): 1285–99. doi: 10.2217/fon-2021-1288
- Korkina Yu.S., Shervashidze M.A., Valiev T.T., Batmanova N.A., Panferova T.R. Successful treatment of pancreatitis caused by L-asparaginase in clinical practice. Oncohematology 2024; 19 (1): 113–24. (In Russ.) doi: 10.17650/1818‐8346‐2024‐191‐113‐124
- Wolthers B.O., Frandsen T.L., Baruchel A., Attarbaschi A., Barzilai S., Colombini A., et al; Ponte di Legno Toxicity Working Group. Asparaginase-associated pancreatitis in childhood acute lymphoblastic leukaemia: an observational Ponte di Legno Toxicity Working Group study. Lancet Oncol. 2017; 18 (9): 1238–48. doi: 10.1016/S14702045(17)30424-2
- General characteristics of Oncaspar (pegaspargase). [Electronic resource] URL: https://servier.ru/wp-content/uploads/2022/02/20220204_SPC_RU_Oncaspar.pdf (access date: 17.02.2024) (In Russ.)].
- Carobolante F., Chiaretti S., Skert C., Bassan R. Practical guidance for the management of acute lymphoblastic leukemia in the adolescent and young adult population. Ther Adv Hematol 2020; 11: 2040620720903531. doi: 10.1177/2040620720903531
- Jörck C., Kiess W., Weigel J.F., Mütze U., Bierbach U., Beblo S. Transient hyperammonemia due to L-asparaginase therapy in children with acute lymphoblastic leukemia or non-Hodgkin lymphoma. Pediatr Hematol Oncol 2011; 28 (1): 3–9. doi: 10.3109/08880018.2010.484852
- Śliwa-Tytko P., Kaczmarska A., Lejman M., Zawitkowska J. Neurotoxicity Associated with Treatment of Acute Lymphoblastic Leukemia Chemotherapy and Immunotherapy. Int J Mol Sci 2022; 23 (10): 5515. doi: 10.3390/ijms23105515
- Truelove E., Fielding A.K., Hunt B.J. The coagulopathy and thrombotic risk associated with L-asparaginase treatment in adults with acute lymphoblastic leukaemia. Leukemia 2013; 27 (3): 553–9. doi: 10.1038/leu.2012.290
- Bettigole R.E., Himelstein E.S., Oettgen H.F., Clifford G.O. Hypofibrinogenemia due to L-asparaginase: studies of fibrinogen survival using autologous 131-I-fibrinogen. Blood 1970; 35 (2): 195–200.
- Korkina Yu.S., Valiev T.T. L-asparaginase: New about Well-Known Drug. Pediatric pharmacology 2021; 18 (3): 227–32. (In Russ.) doi: 10.15690/pf.v18i3.2282
- Diop M., Bangoura M., Barry A., Camara E., Ouo K., Beimy P., et al. Transient Diabetes Induced by L-Asparaginase. Open J Pediatr 2023; 13: 862–5. doi: 10.4236/ojped.2023.136094
- Andino-Lebron K., Aponte A., Laboy I., Mangual M., Mora G., Ortiz-Torres Y., et al. #1707387 Sooner Than Anticipated: L-Asparaginase-Induced Hyperglycemia in an Adult Male – A Case Report, Endocrine Practice 2024; 30 (Issue 5, Suppl): S51–2. doi: 10.1016/j.eprac.2024.03.225
- Kuhlen M., Kunstreich M., Gökbuget N. Osteonecrosis in Adults with Acute Lymphoblastic Leukemia: An Unmet Clinical Need. Hemasphere 2021; 5 (4): e544. doi: 10.1097/HS9.0000000000000544
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