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Methotrexate

Methotrexate (abbreviated MTX; formerly known as amethopterin) is an antimetabolite drug used in treatment of cancer and autoimmune diseases. It acts by inhibiting the metabolism of folic acid. more...

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History

Methotrexate originated in the 1940s when Sidney Farber at Children's Hospital Boston was testing the effects of folic acid on cancer. That inspired chemists at the drug company Lederle to start looking for antimetabolites resembling folic. The result was methotrexate, which was developed in 1948. Methotrexate gained FDA approval as an oncology drug in 1953.

Uses

Methotrexate was originally used, as part of combination chemotherapy regimens, to treat many kinds of cancers. It is still the mainstay for the treatment of many neoplastic disorders including acute lymphoblastic leukemia.

More recently it has come into use as a treatment for some autoimmune diseases, including psoriasis, psoriatic arthritis, rheumatoid arthritis (see disease-modifying antirheumatic drugs), and Crohn's disease. In the case of rheumatoid arthritis, parallel use with infliximab or etanercept has been shown to markedly improve symptoms. (Klareskog, et al., 2004)

Although not licensed for this indication, methotrexate is also sometimes used (generally in combination with misoprostol) to terminate early pregnancies, particularly ectopic pregnancies.

It can be taken orally or administered by injection (intramuscular, intravenous or intrathecal). Although daily preparations are occasionally used, most patients take weekly doses, which decreases the risk of certain side-effects.

Adverse effects

Possible side effects can include anemia, neutropenia, increased risk of bruising, and nausea. A small percentage of patients develop hepatitis, while there is an increased risk of pulmonary fibrosis.

The higher doses of methotrexate often used in cancer chemotherapy can cause toxic effects to the rapidly-dividing cells of bone marrow and gastrointestinal mucosa. The resulting myelosuppression and mucositis are often prevented (termed methotrexate "rescue") by using folinic acid supplements (not to be confused with folic acid).

Methotrexate is a highly teratogenic drug and categorized in Pregnancy Category X by the FDA. Women must not take the drug during pregnancy, if there is a risk of becoming pregnant, or if they are breastfeeding. Men who are trying to get their partner pregnant must also not take the drug. To engage in any of these activities (after discontinuing the drug), women must wait until the end of a full ovulation cycle and men must wait three months.

There is a risk of a severe adverse reaction if penicillin is prescribed alongside methotrexate.

Mode of action

Methotrexate competetively and reversibly inhibits dihydrofolate reductase (DHFR), an enzyme that is part of the folate synthesis metabolic pathway. The affinity of methotrexate for DHFR is about one thousand-fold that of folate for DHFR. Dihydrofolate reductase catalyses the conversion of dihydrofolate to the active tetrahydrofolate. Folic acid is needed for the de novo synthesis of the nucleoside thymidine, required for DNA synthesis. Methotrexate, therefore, inhibits the synthesis of DNA, RNA, thymidylates, and proteins.

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Multidose vs. Single-Dose therapy in pregnancy - Tips from Other Journals - methotrexate for the treatment of ectopic pregnancy - Author Abstract
From American Family Physician, 9/15/03 by Anne D. Walling

Approximately 2 percent of pregnancies in this country are ectopic, a condition that may cause significant hemorrhage and other serious complications. The success rates of medical treatment are comparable to those of surgery, with the added advantages of avoiding anesthetic and surgical risk while retaining fertility. Two protocols are currently used for medical treatment of ectopic pregnancy. "Single-dose" methotrexate therapy is given in a dosage of 50 mg per [m.sup.2] of body surface area. The "multidose" regimen consists of 1 mg per kg of methotrexate, alternating with 0.1 mg per kg of leucovorin, for up to four doses of each agent. Both regimens are effective but have not been compared directly in a clinical trial. Barnhart and colleagues compared evidence for the efficacy and tolerability of single-dose and multidose regimens of methotrexate in the treatment of ectopic pregnancy.

Through electronic and manual searches, the authors identified 213 relevant articles, 26 of which met criteria for quality and inclusion in the analysis. They reviewed 1,327 cases of women with ectopic pregnancy who had been treated with methotrexate. The overall success rate of treatment was 89 percent, with 36 percent of women reporting side effects. In the single-dose group, 14.5 percent of women required more than one dose of methotrexate. In the multidose group, 53.5 percent received four or more doses. The overall success rate in the 1,067 women treated with the single-dose regimen was 88.1 percent compared with 92.7 percent in the 260 women treated with the multidose regimen. Side effects were reported by 31.3 percent of women receiving single-dose therapy and 41.2 percent of those receiving the multidose regimen. Rates of hospital admission were similar in the two groups (12.4 percent for single-dose therapy and 11 percent for multidose therapy).

The authors conclude that although the multidose regimen of methotrexate is associated with significantly more side effects and is more complicated to administer, it is more effective than the single-dose protocol for treatment of unruptured ectopic pregnancy. Because unsuccessful medical treatment could result in hemorrhage, emergency surgery, or even death, the additional efficacy of multidose treatment outweighs the greater convenience and lower rate of side effects associated with single-dose treatment.

Barnhart KT, et al. The medical management of ectopic pregnancy: a meta-analysis comparing "single dose" and "multidose" regimens. Obstet Gynecol April 2003;101: 778-84.

ANNE D. WALLING, M.D.

COPYRIGHT 2003 American Academy of Family Physicians
COPYRIGHT 2003 Gale Group

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