Ate

methotrexate (methopterin, MTX) (meth oh trex' ate) Rheumatrex, Rheumatrex Dose Pak, Trexall Pregnancy Category X Drug classes

Antimetabolite Antineoplastic Antipsoriatic Antirheumatic Therapeutic actions

Inhibits folic acid reductase, leading to inhibition of DNA synthesis and inhibition of cellular replication; selectively affects the most rapidly dividing cells (neoplastic and psoriatic cells). Indications

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Treatment of gestational choriocarcinoma, chorioadenoma destruens, hydatidiform mole Treatment and prophylaxis of meningeal leukemia Symptomatic control of severe, recalcitrant, disabling psoriasis Management of severe, active, classical, or definite rheumatoid arthritis Management of polyarticular course juvenile rheumatoid arthritis Unlabeled uses: High-dose regimen followed by leucovorin rescue for adjuvant therapy of nonmetastatic osteosarcoma (orphan drug designation); to reduce corticosteroid requirements in patients with severe corticosteroid-dependent asthma Orphan drug use: Treatment of juvenile rheumatoid arthritis

Contraindications and cautions

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Contraindicated with pregnancy, lactation, alcoholism, chronic liver disease, immune deficiencies, blood dyscrasias, hypersensitivity to methotrexate. Use cautiously with renal disease, infection, peptic ulcer, ulcerative colitis, debility.

Available forms

Tablets—2.5, 5, 7.5, 10, 15 mg; powder for injection—20 mg, 50 mg, 1 g per vial; injection—25 mg/mL, 2.5 mg/mL; preservative-free injection—25 mg/mL Dosages ADULTS

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Choriocarcinoma and other trophoblastic diseases: 15–30 mg PO or IM daily for a 5-day course. Repeat courses 3–5 times with rest periods of 1 wk or more between courses until toxic symptoms subside. Continue 1–2 courses of methotrexate after chorionic gonadotropin hormone levels are normal.

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Leukemia: Induction: 3.3 mg/m2 of methotrexate PO or IM with 60 mg/m2 of prednisone daily for 4–6 wk. Maintenance: 30 mg/m2 methotrexate PO or IM twice weekly or 2.5 mg/m2 IV every 14 days. If relapse occurs, return to induction doses. Meningeal leukemia: Give methotrexate intrathecally in cases of lymphocytic leukemia as prophylaxis. 12 mg/m2 intrathecally at intervals of 2–5 days and repeat until cell count of CSF is normal. Lymphomas: Burkitt's tumor, stages I and II: 10–25 mg/day PO for 4–8 days. In stage III, combine with other neoplastic drugs. All usually require several courses of therapy with 7- to 10-day rest periods between doses. Mycosis fungoides: 2.5–10 mg/day PO for weeks or months or 50 mg IM once weekly or 25 mg IM twice weekly. Osteosarcoma: Starting dose is 12 g/m2 or up to 15 g/m2 PO, IM, or IV to give a peak serum concentration of 1,000 micromol. Must be used as part of a cytotoxic regimen with leucovorin rescue. Severe psoriasis: 10–25 mg/wk PO, IM, or IV as a single weekly dose. Do not exceed 50 mg/wk or 2.5 mg PO at 12-hr intervals for 3 doses or at 8-hr intervals for 4 doses each wk. Do not exceed 30 mg/wk. Alternatively, 2.5 mg/day PO for 5 days followed by at least 2 days rest. Do not exceed 6.25 mg/day. After optimal clinical response is achieved, reduce dosage to lowest possible with longest rest periods and consider return to conventional, topical therapy. Severe rheumatoid arthritis: Starting dose: single doses of 7.5 mg/wk PO or divided dosage of 2.5 mg PO at 12-hr intervals for 3 doses given as a course once weekly. Dosage may be gradually increased, based on response. Do not exceed 20 mg/wk. Therapeutic response usually begins within 3–6 wk, and improvement may continue for another 12 wk. Improvement may be maintained for up to 2 yr with continued therapy.

PEDIATRIC PATIENTS

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Meningeal leukemia: < 1 yr: 6 mg intrathecally q 2–5 days. 1–2 yr: 8 mg intrathecally q 2–5 days. 2–3 yr: 10 mg intrathecally q 2–5 days. > 3 yr: 12 mg intrathecally q 2–5 days. Polyarticular course juvenile rheumatoid arthritis (2–16 yr): Initially, 10 mg/m2 PO weekly. Dosage may be increased based on patient response. Maximum 20 mg/m2/wk. Therapeutic response usually begins in 3–6 wk.

Pharmacokinetics Route Oral IM, IV

Onset Varies Rapid

Peak 1–4 hr 0.5–2 hr

Metabolism: T1/2: 2–4 hr Distribution: Crosses placenta; enters breast milk Excretion: Urine

IV facts

Preparation: Reconstitute 20- and 50-mg vials with an appropriate sterile preservativefree medium, 5% dextrose solution or sodium chloride injection to a concentration no greater than 25 mg/mL; reconstitute 1-g vial with 19.4 mL to a concentration of 50 mg/mL. Infusion: Administer diluted drug by direct IV injection at a rate of not more than 10 mg/min. Incompatibilities: Do not combine with bleomycin, fluorouracil, prednisolone. Y-site incompatibility: Do not give with droperidol. Adverse effects

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CNS: Headache, drowsiness, blurred vision, aphasia, hemiparesis, paresis, seizures, fatigue, malaise, dizziness Dermatologic: Erythematous rashes, pruritus, urticaria, photosensitivity, depigmentation, alopecia, ecchymosis, telangiectasia, acne, furunculosis GI: Ulcerative stomatitis, gingivitis, pharyngitis, anorexia, nausea, vomiting, diarrhea, hematemesis, melena, GI ulceration and bleeding, enteritis, hepatic toxicity GU: Renal failure, effects on fertility (defective oogenesis, defective spermatogenesis, transient oligospermia, menstrual dysfunction, infertility, abortion, fetal defects) Hematologic: Severe bone marrow depression, increased susceptibility to infection Hypersensitivity: Anaphylaxis, sudden death Respiratory: Interstitial pneumonitis, chronic interstitial obstructive pulmonary disease Other: Chills and fever, metabolic changes (diabetes, osteoporosis), cancer

Interactions

Drug-drug • Increased risk of toxicity with salicylates, phenytoin, probenecid, sulfonamides • Decreased serum levels and therapeutic effects of digoxin • Potentially serious to fatal reactions when given with NSAIDs. Use extreme caution if this combination is used • Risk of toxicity if combined with alcohol; avoid this combination Nursing considerations Assessment

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History: Allergy to methotrexate, hematopoietic depression, severe hepatic or renal disease, infection, peptic ulcer, ulcerative colitis, debility, psoriasis, pregnancy, lactation Physical: Weight; T; skin lesions, color; hair; vision, speech, orientation, reflexes, sensation; R, adventitious sounds; mucous membranes, liver evaluation, abdominal exam; CBC, differential; renal and liver function tests; urinalysis, blood and urine glucose, glucose tolerance test, chest x-ray

Interventions

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Arrange for tests to evaluate CBC, urinalysis, renal and liver function tests, chest x-ray before therapy, during therapy, and for several weeks after therapy. Ensure that patient is not pregnant before administering this drug; counsel patient about the severe risks of fetal abnormalities associated with this drug. Reduce dosage or discontinue if renal failure occurs. Reconstitute powder for intrathecal use with preservative-free sterile sodium chloride injection; intended for one dose only; discard remainder. The solution for injection contains benzyl alcohol and should not be given intrathecally. Arrange to have leucovorin readily available as antidote for methotrexate overdose or when large doses are used. In general, doses of leucovorin (calcium leucovorin) should be equal or higher than doses of methotrexate and should be given within the first hour. Up to 75 mg IV within 12 hr, followed by 12 mg IM q 6 hr for 4 doses. For average doses of methotrexate that cause adverse effects, give 6–12 mg leucovorin IM, q 6 hr for 4 doses or 10 mg/m2 PO followed by 10 mg/m2 q 6 hr for 72 hr. Arrange for an antiemetic if nausea and vomiting are severe. Arrange for adequate hydration during therapy to reduce the risk of hyperuricemia. Do not administer any other medications containing alcohol.

Teaching points

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Prepare a calendar of treatment days. This drug may cause birth defects or miscarriages. Use birth control while on this drug and for 8 wk thereafter. Males using this drug should also use barrier contraceptives. Avoid alcohol; serious side effects may occur. Arrange for frequent, regular medical follow-up visits, including blood tests to follow the drug's effects. These side effects may occur: Nausea, vomiting (request medication; eat frequent small meals); numbness, tingling, dizziness, drowsiness, blurred vision, difficulty speaking (drug effects; seek dosage adjustment; avoid driving or operating dangerous machinery); mouth sores (frequent mouth care is needed); infertility; loss of hair (obtain a wig or other suitable head covering; keep the head covered at extremes of temperature); rash, sensitivity to sun and ultraviolet light (avoid sun; use a sunscreen and protective clothing). Report black, tarry stools; fever; chills; sore throat; unusual bleeding or bruising; cough or shortness of breath; darkened or bloody urine; abdominal, flank, or joint pain; yellow color to the skin or eyes; mouth sores.

Adverse effects in Italic are most common; those in Bold are life-threatening.