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Practice

Low-dose methotrexate toxicity

Kevin Pivovarov and Jonathan S. Zipursky
CMAJ April 15, 2019 191 (15) E423; DOI: https://doi.org/10.1503/cmaj.181054
Kevin Pivovarov
Department of Medicine (Pivovarov, Zipursky), University of Toronto; Division of Internal Medicine (Pivovarov), Mount Sinai Hospital; Division of Clinical Pharmacology and Toxicology (Zipursky), Sunnybrook Health Sciences Centre, Toronto, Ont.
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Jonathan S. Zipursky
Department of Medicine (Pivovarov, Zipursky), University of Toronto; Division of Internal Medicine (Pivovarov), Mount Sinai Hospital; Division of Clinical Pharmacology and Toxicology (Zipursky), Sunnybrook Health Sciences Centre, Toronto, Ont.
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Methotrexate is used at low doses for the treatment of autoimmune and inflammatory disorders

Low-dose methotrexate is an effective first-line treatment for early rheumatoid arthritis and other inflammatory arthropathies,1 and as a maintenance therapy in Crohn disease, vasculitis and refractory atopic dermatitis. The usual dose is 5 to 25 mg once weekly. Patients should take folic acid (1 mg) on days they are not taking methotrexate to prevent folate depletion.

Complete blood count, liver and renal function should be monitored during treatment

Before starting treatment, liver and kidney disease should be excluded, and screening done for alcohol use. Pretreatment investigations should include baseline complete blood count, assessment of liver and renal function, chest radiograph and pregnancy test (in women of childbearing age).2 Complete blood count, creatinine and liver function test should be assessed every 2–4 weeks for the first 3 months, then 8–12 weeks for the following 3–6 months, and every 12 weeks thereafter.1

Toxicity can cause bone marrow, hepatic and pulmonary disorders

Pancytopenia occurs in less than 1% of patients and typically resolves after stopping treatment.3 Hepatotoxicity ranges from mild steatosis to severe fibrosis and cirrhosis, and is associated with long-term use, obesity, diabetes and alcohol use.3 Pulmonary toxicity occurs in less than 8% of patients, usually within the first year of treatment.3 Painful stomatitis and gastrointestinal upset are the most common minor adverse effects.3 See Appendix 1 (available at www.cmaj.ca/lookup/suppl/doi:10.1503/cmaj.181054/-/DC1) for reasons to re-evaluate therapy.

Decreased clearance, drug–drug interactions and dosing errors are risk factors for toxicity

Additionally, hypoalbuminemia and renal failure increase the risk of toxicity.3 Toxicity can occur with the combination of trimethoprim-sulfamethoxazole and methotrexate because both inhibit folate metabolism; prophylactic doses of trimethoprim-sulfamethoxazole are considered safe.3 Patients may mistakenly take doses daily instead of weekly, and because folate and methotrexate tablets look similar, one tablet may be mistaken for the other (Appendix 2, available at www.cmaj.ca/lookup/suppl/doi:10.1503/cmaj.181054/-/DC1).

Folic acid or folinic acid (leucovorin) is used to prevent and treat toxicity

Folic acid decreases the risk of gastrointestinal adverse effects by 9%, elevated liver function tests by 16%, and rates of drug discontinuation by 15%.4 With gastrointestinal upset, the dose can be increased to 5 mg. Leucovorin (2.5 mg to 5 mg once weekly) can be given to mitigate adverse effects, including stomatitis, when higher doses of folic acid have failed. It treats toxicity by bypassing methotrexate inhibition of dihydrofolate reductase, the enzyme required to reduce folate to tetrahydrofolate.4

Acknowledgements

The authors thank Jennifer Do BscPhm RPh (Sunnybrook Health Sciences Centre) and Tina Hwu BscPhm RPh (Mount Sinai Hospital) for their insights into the prescribing and dispensing of methotrexate in Canadian pharmacies, and for comments on earlier versions of this manuscript.

Footnotes

  • Competing interests: None declared.

  • This article has been peer reviewed.

References

  1. ↵
    1. Singh JA,
    2. Saag KG,
    3. Bridges SL Jr.,
    4. et al
    . 2015 American College of Rheumatology guideline for the treatment of rheumatoid arthritis. Arthritis Rheumatol 2016;68:1–26.
    OpenUrl
  2. ↵
    1. Bykerk VP,
    2. Akhavan P,
    3. Hazlewood GS,
    4. et al.
    Canadian Rheumatology Association. Canadian Rheumatology Association recommendations for pharmacological management of rheumatoid arthritis with traditional and biologic disease-modifying antirheumatic drugs. J Rheumatol 2012;39:1559–82.
    OpenUrlAbstract/FREE Full Text
  3. ↵
    1. Romão VC,
    2. Lima A,
    3. Bernardes M,
    4. et al
    . Three decades of low-dose methotrexate in rheumatoid arthritis: Can we predict toxicity? Immunol Res 2014;60:289–310.
    OpenUrl
  4. ↵
    1. Shea B,
    2. Swinden MV,
    3. Tanjong Ghogomu E,
    4. et al
    . Folic acid and folinic acid for reducing side effects in patients receiving methotrexate for rheumatoid arthritis. Cochrane Database Syst Rev 2013;(5): CD000951.
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Canadian Medical Association Journal: 191 (15)
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15 Apr 2019
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Low-dose methotrexate toxicity
Kevin Pivovarov, Jonathan S. Zipursky
CMAJ Apr 2019, 191 (15) E423; DOI: 10.1503/cmaj.181054

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Low-dose methotrexate toxicity
Kevin Pivovarov, Jonathan S. Zipursky
CMAJ Apr 2019, 191 (15) E423; DOI: 10.1503/cmaj.181054
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    • Methotrexate is used at low doses for the treatment of autoimmune and inflammatory disorders
    • Complete blood count, liver and renal function should be monitored during treatment
    • Toxicity can cause bone marrow, hepatic and pulmonary disorders
    • Decreased clearance, drug–drug interactions and dosing errors are risk factors for toxicity
    • Folic acid or folinic acid (leucovorin) is used to prevent and treat toxicity
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