Methotrexate (MTx), Serum

Specimen requirement Adult patient:

  Clotted blood tube (Serum gel separator clot activator tube)

Minimum blood volume: 5 mL

Paediatric patient:

Paediatric clotted blood tube

Number of vials: 2

Minimum blood volume: 1.6 mL

Authorisation code required No
24 Hr available service No
Precaution Samples should be protected from light.
Method Immunoassay
Reference interval

Toxic level:

 

at 24 Hr > 5.0 µmol/L

at 48 Hr > 0.5 µmol/L

at 72 Hr > 0.1 µmol/L

 

(Source: from manufacturer's kit insert)

Clinical indication

Monitoring levels of methotrexate to ensure appropriate therapy.

Result interpretation

Methotrexate is an antineoplastic drug used solely or in combination with other antineoplastic drugs for the treatment of leukemia and other diseases.

Relatively low doses of methotrexate (approximately 7.5 - 25 mg/week) have been used in the treatment of nonmalignant diseases such as severe psoriasis, asthma, rheumatoid arthritis, sarcoidosis, and transplantation therapy.

Intermediate to high doses of methotrexate (approximately 35 mg/m2 - 12 g/m2) with leucovorin (citrovorum-factor) rescue have been used with favourable results in the treatment of osteogenic sarcoma, leukemia, non-Hodgkin's lymphoma, lung and breast cancer.

Sampling time of methotrexate will be dependent on dose, duration of infusion, and clinical status of the patient.

Following a 4 - 6 Hr intravenous methotrexate infusion with dosages ranging from 50 mg/m2  - 15 g/m2, a patient with a 24 Hr serum concentration of greater than 5 - 10 µmol/L, a 48 Hr level greater than 0.5 - 1.0 µmol/L, and a 72 Hr level greater than 0.2 µmol/L is at an increased risk of toxicity if conventional low-dose leucovorin rescue is given.

Measurement of uncertainty See table.
Frequency of measurement Daily