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Methotrexate (MTX), Serum or Plasma

CPT 80204
Synonyms
  • Rheumatrex®
  • Trexall™

Test Details

Methodology

Liquid chromatography/tandem mass spectrometry (LC/MS-MS)

Result Turnaround Time

2 - 4 days

Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.

Related Documents

Use

Methotrexate, either alone or in combination regimens depending on the patient's risk factors, have been very effective in women with choriocarcinoma and related trophoblastic tumors. Cures have been reported in most individuals treated with low doses of methotrexate plus leucovorin.

Although methotrexate induces complete remissions in acute lymphocytic leukemia of childhood, it is of more value for maintenance therapy and is an agent of choice in combination with mercaptopurine. Furthermore, intrathecal methotrexate and cranial irradiation are administered routinely to patients with acute lymphocytic leukemia to prevent meningeal metastases.

Methotrexate is a component of combination regimens used to treat non-Hodgkin and Burkitt lymphomas and breast, lung, bladder, cervical, gastric, and ovarian carcinomas. High-dose methotrexate plus leucovorin rescue (with or without other drugs) is used to treat osteogenic sarcoma, some non-Hodgkin lymphomas, and (by some physicians) head and neck tumors.

Methotrexate is a primary agent in the treatment of cutaneous T-cell lymphomas and medulloblastoma. It has shown activity as a single agent against testicular cancer; bladder, lung, colorectal, esophageal, hepatocellular, and cervical carcinomas; soft tissue sarcomas; and embryonal rhabdomyosarcoma. For some of these neoplasms (testicular, colorectal, and hepatocellular cancers; soft tissue sarcomas and rhabdomyosarcoma) more effective regimens are available and are used much more frequently than methotrexate.

Limitations

This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.

References

American Medical Association, Division of Drugs and Toxicology. Drug Evaluations Subscription. Chicago, Ill: AMA, Spring, 1993.

Custom Additional Information

Methotrexate is an antimetabolite that combines with dihydrofolate reductase and therefore interferes with the synthesis of tetrahydrofolic acid necessary for DNA synthesis. From 40% to 50% of a small dose and up to 90% of a larger dose is excreted unchanged in the urine in 48 hours, a major portion of it during the first eight hours. Toxicity consists of bone marrow depression with megaloblastosis. Concomitant salicylate administration increases incidence of toxicity, due to diminished renal tubular excretion. The effect of methotrexate on normal cells may be reversed by administration of 5-formyltetrahydrofolate, also called citrovorum factor or leucovorin. This “rescue” makes possible administration of much higher doses of methotrexate than the body would otherwise survive. The initial half-life is two to four hours but the total body clearance (terminal) half-life is 8 to 15 hours.

Specimen Requirements

Specimen

Serum or plasma

Volume

1 mL

Minimum Volume

0.3 mL

Container

Red-top tube, lavender-top (EDTA) tube, or green-top (heparin) tube. Do not use a gel-barrier tube. The use of gel-barrier tubes is not recommended due to slow absorption of the drug by the gel. Depending on the specimen volume and storage time, the decrease in drug level due to absorption may be clinically significant.

Collection Instructions

Transfer separated serum or plasma to a plastic transport tube. Collection is determined by dosing protocol.

Stability Requirements

Temperature

Period

Room temperature

14 days

Refrigerated

14 days

Frozen

14 days

Freeze/thaw cycles

Stable x3

Reference Range

Therapeutic: 0.02−5.00 μmol/L

Storage Instructions

Room temperature

Causes for Rejection

Gel-barrier tube

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
007658 Methotrexate (MTX), Serum 14836-1 007658 Methotrexate (MTX), Serum umol/L 14836-1
Order Code007658
Order Code NameMethotrexate (MTX), Serum
Order Loinc14836-1
Result Code007658
Result Code NameMethotrexate (MTX), Serum
UofMumol/L
Result LOINC14836-1