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This is a PatientPlus article. PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people.

Synonyms: asparaginase

Crisantaspase is an enzyme, asparaginase, derived from the bacterium Erwinia chrysanthemi. A lot of progress in the treatment of acute lymphoblastic leukaemias has been made over the last 30 years using combinations of drugs including crisantaspase.1 Now 80% of patients can be cured, although clinical subgroups with a poor prognosis can be identified (for example those with central nervous system disease).2

Mode of action

Asparagine is important for protein synthesis in leukaemia cells (it cannot be synthesised without the enzyme asparaginase synthase). Crisantaspase (asparaginase) depletes leukaemia cells of asparagine so blocking protein synthesis and cell proliferation. It also causes apoptosis. In many cases patients develop drug-resistant forms of the disease which correlate with up-regulation of the enzyme glutamine dependent asparagine synthetase, although may not be linked directly to the up-regulation.3 Newer derivatives of the drug are proving useful in the treatment of relapsed or refractory leukaemias.4,5

Indications

Crisantaspase is a major component of regimens for the treatment of acute lymphoblastic leukaemia (ALL), particularly in children, but some debate exists about the best formulation and dosage.6 It is a crucial drug in the induction therapy for ALL. It should be used as part of regimens designed and initiated in specialist treatment centres.

Drug initiation and administration

It is given intravenously through central or peripheral line but can also be given intramuscularly and subcutaneously. Asparaginase derived from E. coli has been found to be superior but more toxic than that derived from Erwinia chrysanthemi. 6 A review of the different types shows that newer preparations show advantages over older, native preparations.5,7,8

Guidelines for handling cytotoxic drugs

  • Trained personnel should 'make up' or reconstitute cytotoxics.
  • Reconstitution should be carried out in designated areas.
  • Protective clothing should be worn (for example gloves, gown and masks).
  • The eyes should be protected.
  • First aid procedures and equipment should be in place.
  • Pregnant staff should avoid exposure to cytotoxic drugs and all females of child-bearing age should be informed of the hazard posed.
  • Follow local procedures for safe disposal of waste material (for example syringes, containers and dressings).
  • Staff exposure to cytotoxic drugs should be monitored.

Common cautions and contraindications

Pregnancy and breastfeeding.

Common interactions

Caution with aspirin and anticoagulants. Crisantaspase affects production of clotting factors in the liver and thus may cause changes in blood clotting, occasionally with bruising or bleeding. Such effects may be exacerbated with concomitant use of aspirin or anticoagulants.

Side-effects
  • Itchy rash and fever occur commonly.
  • Other significant side effects include:
    • Nausea and vomiting.
    • Loss of appetite.
    • Coagulation disorders (causing bruising and bleeding).
    • Liver function changes.
    • Pancreatitis.
    • Hyperglycaemia.
    • Lipid changes.
  • As it is a protein, allergic reactions can occur.
  • Hair loss is not a problem with crisantaspase.
Monitoring

This should be coordinated in specialist treatment centres and incorporate monitoring of the disease being treated as well as monitoring for adverse effects of treatment. Patients are warned of symptoms of hyperglycaemia (thirst, polyuria) and given instructions in testing for glycosuria. Facilities for the management of anaphylaxis should be available when administered.

Practice tips

Shared care protocols with details of the drug regimens and detail about drugs within the particular regimen should be sought from the treatment centres.


Document references
  1. Richards NG, Kilberg MS; Asparagine synthetase chemotherapy. Annu Rev Biochem. 2006;75:629-54. [abstract]
  2. Moricke A, Zimmermann M, Reiter A, et al; Prognostic impact of age in children and adolescents with acute lymphoblastic leukemia: data from the trials ALL-BFM 86, 90, and 95. Klin Padiatr. 2005 Nov-Dec;217(6):310-20. [abstract]
  3. Appel IM, den Boer ML, Meijerink JP, et al; Up-regulation of asparagine synthetase expression is not linked to the clinical response L-asparaginase in pediatric acute lymphoblastic leukemia. Blood. 2006 Jun 1;107(11):4244-9. Epub 2006 Feb 23. [abstract]
  4. Corey SJ; New agents in the treatment of childhood leukemias and myelodysplastic syndromes.; Curr Oncol Rep. 2005 Nov;7(6):399-405. [abstract]
  5. Avramis VI, Panosyan EH; Pharmacokinetic/pharmacodynamic relationships of asparaginase formulations: the past, the present and recommendations for the future. Clin Pharmacokinet. 2005;44(4):367-93. [abstract]
  6. Nga Kwok CS, Yin Kham SK, Ariffin H, et al; Minimal residual disease (MRD) measurement as a tool to compare the efficacy of chemotherapeutic drug regimens using Escherichia Coli-asparaginase or Erwinia-asparaginase in childhood acute lymphoblastic leukemia (ALL). Pediatr Blood Cancer. 2005 Nov 21. [abstract]
  7. Narta UK, Kanwar SS, Azmi W; Pharmacological and clinical evaluation of L-asparaginase in the treatment of leukemia. Crit Rev Oncol Hematol. 2007 Mar;61(3):208-21. Epub 2006 Oct 2. [abstract]
  8. Richards NG, Kilberg MS; Asparagine Synthetase Chemotherapy. Annu Rev Biochem. 2006 Mar 10;. [abstract]
AcknowledgementsEMIS is grateful to Dr Richard Draper for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2009.
Document ID: 810
Document Version: 3
Document Reference: bgp26090
Last Updated: 6 May 2009
Planned Review: 6 May 2011

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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