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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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Comparison of abortions induced by methotrexate or mifepristone followed by misoprostol - Brief Article
From Journal of Family Practice, 3/1/02 by Ellen Wiebe

* BACKGROUND Mifepristone has recently been approved in the US but is still unavailable in Canada and many other countries. Mifepristone is much more expensive than methotrexate, which is widely available. No other study has compared these 2 early abortion methods.

* OBJECTIVE To compare methotrexate with mifepristone when used to induce abortion with respect to effectiveness, side effects, and acceptability.

* STUDY DESIGN A randomized, nonblinded controlled trial.

* POPULATION Participants were 1001 women aged 16 years and older at 49 days' gestation or less who presented for abortion at 5 abortion clinics across Canada. We compared 2 groups: 50 mg/[m.sup.2] methotrexate followed 4 to 6 days later by 800 [micro]g vaginal misoprostol (n=505) vs 600 mg mifepristone orally in 1 dose followed 36 to 48 hours later by 400 [micro]g oral misoprostol (n=494).

* OUTCOMES MEASURED Rates of surgery, days to complete abortion, pain scores, days of bleeding, side effects, complications, and acceptability.

* RESULTS In the methotrexate group, 20 women had surgery; in the mifepristone group, 22. By day 8, only 374 women in the methotrexate group experienced completed abortion vs 453 in the mifepristone group. The mean number of days from beginning to completion was 6.9 for methotrexate and 3.2 for mifepristone (P = .000). The mean worst pain on a scale from 0 to 10 was 6.4 for methotrexate and 5.8 for mifepristone (P = .001). The mean number of days of bleeding was 12.8 for methotrexate and 14.6 for mifepristone (P = .005). There were no differences in complications. Eleven women visited a hospital; 22 were treated for excessive bleeding, although none needed a transfusion; and 8 received antibiotics for possible infection. Side effects were similar. Acceptance was slightly higher with mifepristone (413 / 466) than with methotrexate (389 / 464).

* CONCLUSIONS Abortions induced with mifepristone were completed faster than those induced with methotrexate. Overall success rates, side effects, and complications were similar. Acceptance rates were slightly higher with mifepristone than with methotrexate.

COPYRIGHT 2002 Appleton & Lange
COPYRIGHT 2002 Gale Group

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