Voraxaze (glucarpidase)
Methotrexate Rescue Agents - Carboxypeptidase G2 Type Intravenous Vial (Ea)
Last reviewed · Source: First Databank (FDB) drug data
Overview
Glucarpidase (also known as carboxypeptidase G2 (CPDG2)) is a recombinant bacterial enzyme that is used as an antidote for methotrexate toxicity.
Glucarpidase (also known as carboxypeptidase G2 (CPDG2)) is a bacterial enzyme produced by recombinant DNA technology. Glucarpidase was isolated from the Pseudomonas strain RS-16 and cloned, purified, and sequenced in genetically modified Escherichia coli. Glucarpidase rapidly hydrolyzes the carboxyl-terminal glutamate residue of folic acid, folic acid derivatives, and classic antifolates (e.g., methotrexate, leucovorin); the drug converts methotrexate to its inactive metabolites 4-deoxy-4-amino-N10-methylpteroic acid (DAMPA) and glutamate, which are metabolized principally by the liver.
Following administration of glucarpidase (50 units/kg) in the pivotal single-arm, open-label study, plasma methotrexate concentrations (measured by chromatographic method) were reduced by at least 97% within 15 minutes in all 22 treatment-evaluable patients and were maintained at a greater than 95% reduction for up to 8 days in 20 of the 22 patients.
Because of the large molecular size of glucarpidase, the drug is distributed primarily in the intravascular (i.e., extracellular) compartment and does not directly reduce intracellular concentrations (or interfere with intracellular antineoplastic effects) of methotrexate; therefore, rescue therapy with leucovorin must be continued following administration of glucarpidase. (See Methotrexate Toxicity under Dosage and Administration: Dosage and also see Drug Interactions: Reduced Folates.) Reductions in plasma methotrexate concentrations produced by glucarpidase are expected to cause redistribution (i.e., efflux) of intracellular methotrexate back into plasma, resulting in a rise in plasma methotrexate concentrations; as such, small rebound increases in plasma methotrexate concentrations have been observed in patients receiving glucarpidase in clinical studies.
The mean elimination half-life of glucarpidase is 5.6 hours (as assessed by enzymatic assay) or 9 hours (as assessed by enzyme-linked immunosorbent assay (ELISA)).
Generic name: glucarpidase
Drug class: Methotrexate Rescue Agents - Carboxypeptidase G2 Type
Therapeutic class: Antineoplastics
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Voraxaze
Indications
The following indications are listed for Voraxaze:
- Methotrexate Toxicity
Also known as: Mtx Toxicity.
Dosing
Dosage of glucarpidase is expressed in terms of units; a unit of glucarpidase activity is defined as the quantity of enzyme needed to catalyze the hydrolysis of 0.454 mcg/mL (1 mcmol/L) of methotrexate per minute at 37degreesC.
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Drug interactions
There is no enhanced messaging for this drug.
There are no contraindication interactions for this drug.
There are no severe interactions for this drug.
Moderate Interaction: Assess the risk to the patient and take action as needed.
Glucarpidase/Levoleucovorin; Leucovorin
SEVERITY LEVEL: 3-Moderate Interaction: Assess the risk to the patient and take action as needed.
MECHANISM OF ACTION: Glucarpidase hydrolyzes the carboxyl-terminal glutamate residue from folates such as leucovorin, rendering them inactive.(1)
CLINICAL EFFECTS: A leucovorin dose given near the time of glucarpidase administration may not be effective.
PREDISPOSING FACTORS: Leucovorin dose given within two hours of glucarpidase administration.
PATIENT MANAGEMENT: The combination of glucarpidase and leucovorin are used to treat toxic concentrations of methotrexate. Patients with potentially life threatening methotrexate serum levels or toxicity must receive both drugs. However, in addition to inactivating methotrexate, glucarpidase also inactivates leucovorin. To help decrease leucovorin inactivation, stagger leucovorin administration so it is not given within two hours of glucarpidase dose. Continue leucovorin treatment based upon pre-glucarpidase methotrexate blood levels.(1) Note that depending upon the laboratory assay used, glucarpidase administration may cause erroneous methotrexate measurements for 48 hours post dose.(1)
DISCUSSION: In a study of cancer patients treated with a high dose methotrexate and leucovorin rescue regimen, glucarpidase given two hours before leucovorin reduced the area-under-curve (AUC) of the active leucovorin metabolite, 5-methyltetrahydrofolate, by 92 per cent.(1)
Contraindications
The manufacturer states there are no known contraindications to the use of glucarpidase.
There are no contraindication contraindications for this drug.
There are no severe contraindications for this drug.
- No disease contraindications
Adverse reactions
Adverse effects reported in 1% or more of patients receiving glucarpidase include paresthesia, flushing, nausea and/or vomiting, hypotension, and headache.
Rare or Very Rare
- Anaphylaxis
- Throat constriction
Less Frequent
- Flushing
- Headache disorder
- Hypotension
- Nausea
- Paresthesia
- Vomiting
Rare or Very Rare
- Blurred vision
- Diarrhea
- Hypertension
- Skin rash
- Tremor
Precautions
No enhanced messaging available.
Efficacy of glucarpidase as adjunctive therapy for the treatment of toxic plasma methotrexate concentrations (exceeding 0.454 mcg/mL (1 mcmol/L)) in pediatric patients with delayed methotrexate clearance due to renal impairment has been established in one study that included 12 patients 5-16 years of age. In this study, 3 of the 6 pediatric patients with pre-glucarpidase plasma methotrexate concentrations of 0.454-22.7 mcg/mL (1-50 mcmol/L) achieved rapid and sustained clinically important reductions (RSCIR) in plasma methotrexate concentrations, while none of the remaining 6 patients with pre-glucarpidase plasma methotrexate concentrations exceeding 22.7 mcg/mL (50 mcmol/L) achieved RSCIR.
In an analysis of pooled clinical safety data in 147 patients 1 month to 17 years of age, no overall difference in safety was observed between pediatric and adult patients.
Category C. (See Users Guide.)
It is not known whether glucarpidase is distributed into human milk. Caution is advised when glucarpidase is administered in nursing women.
In clinical studies, 15% of patients were 65 years of age or older and 4% were 75 years of age or older. No overall differences in safety or efficacy were observed between geriatric patients and younger adults.
ICD codes
No ICD codes are available for this drug.
Formulary status
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Last reviewed · Source: First Databank (FDB) drug data
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