Pegaspargase
Brand names: Oncaspar
Pegaspargase is a specialist parenteral enzyme used as a component of combination chemotherapy in the treatment of acute lymphoblastic leukaemia.
Adult dose
Dose auto-extracted from US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- History of serious hypersensitivity reactions, including anaphylaxis, to pegaspargase or to any of the excipients
- History of serious thrombosis with prior L-asparaginase therapy
- History of pancreatitis, including pancreatitis related to prior L-asparaginase therapy
- History of serious haemorrhagic events with prior L-asparaginase therapy
- Severe hepatic impairment
Side effects
- Hypoalbuminaemia
- Elevated transaminases
- Febrile neutropenia
- Hypertriglyceridaemia
- Hyperglycaemia
Interactions
- Glucocorticoids — pegaspargase may increase the risk of glucocorticoid-induced toxicities (e.g. osteonecrosis) through a potential increase in dexamethasone exposure
Clinical monograph
How it works
It is a pegylated form of L-asparaginase that depletes circulating asparagine, which leukaemic lymphoblasts cannot synthesise, thereby starving them of this amino acid and inhibiting protein synthesis.
Prescribing in practice
- Serious hypersensitivity and anaphylaxis can occur, so it must be given where resuscitation facilities are available and patients observed after administration.
- It can cause pancreatitis, coagulation disturbances with thrombosis or bleeding, and hyperglycaemia, all of which require monitoring.
- Hepatotoxicity may occur and treatment should be administered only under specialist supervision.
Monitoring
Monitor coagulation parameters, blood glucose, amylase or lipase and liver function during treatment.
Counselling the patient
- Report severe abdominal pain, excessive thirst, or any rash, swelling or breathing difficulty.
- Attend for the blood tests arranged to check clotting and blood sugar.
Evidence & guidelines
Use is guided by the Summary of Product Characteristics and established paediatric and adult leukaemia treatment protocols.
Reference: NICE TA408; UKALL trial protocols; ESMO; SmPC; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Acute Myeloid Leukaemia Presentation · BSH; NICE — NG146
- Tumour Lysis Syndrome · Cairo-Bishop; BSH; NICE — Best Practice
- Major Haemorrhage / Massive Transfusion · BCSH; RCOA; RCEM; RCS — BCSH Guidelines
- Anaemia Investigation · BSH / NICE
- Splenomegaly Workup · BSH; BMJ Best Practice
- Deep Vein Thrombosis Diagnosis and Treatment · NICE CG144 / NICE NG158