Methotrexate Cutaneous Ulceration: A Systematic Review of Cases.


Journal

American journal of clinical dermatology
ISSN: 1179-1888
Titre abrégé: Am J Clin Dermatol
Pays: New Zealand
ID NLM: 100895290

Informations de publication

Date de publication:
Jul 2022
Historique:
accepted: 27 03 2022
pubmed: 30 4 2022
medline: 2 8 2022
entrez: 29 4 2022
Statut: ppublish

Résumé

Methotrexate cutaneous ulceration is a rare methotrexate complication, and has only been described in case reports and case series. To document patient characteristics, morphologic features, and mortality risk factors for methotrexate cutaneous ulceration. A systematic literature review of PubMed and Embase (last date 1 November 2021) was performed with data collected from case reports and case series. This study was limited to cases of cutaneous ulceration; presence of oral ulceration was collected from within these cases. 114 cases (men = 57.9%, mean age = 61 years) of methotrexate cutaneous ulceration met inclusion criteria. Psoriasis (69.3%), rheumatoid arthritis (18.4%), and mycosis fungoides (6.1%) were the most common indications for methotrexate use. Morphologies included erosions localized to psoriatic plaques (33.3%), epidermal necrosis/necrolysis (35.1%), localized ulceration (16.7%), and skin-fold erosions (5.3%). Methotrexate dose preceding toxicity varied greatly; median 20 mg/week, interquartile range 15-40 mg/week, range 5-150 mg/week. Most patients had risk factors for serum toxicity (baseline renal dysfunction = 37.8%, concurrent NSAID use = 28.1%, inadequate folic acid use = 89.1%). Thirty percent of cases involved mistakenly high methotrexate doses. Fourteen patients (12%) died. Absence of folic acid use (69% vs. 100%, p value < 0.001), pancytopenia (33% vs. 86%, p value < 0.001), and renal dysfunction at presentation (47% vs. 92%, p value < 0.001) were associated with increased mortality. Selection bias present due to abstraction from case reports and case series. Methotrexate cutaneous ulceration is commonly preceded by dosage mistakes, absence of folic acid supplementation, and concurrent use of nephrotoxic medications. Renal impairment, pancytopenia, and absence of folic acid supplementation are key risk factors for mortality from this adverse medication reaction. Providers should regularly monitor methotrexate dosing adherence, drug-drug interactions, and perform routine laboratory evaluation. Index of suspicion for this toxicity should remain high given the varied clinical presentation and high mortality.

Sections du résumé

BACKGROUND BACKGROUND
Methotrexate cutaneous ulceration is a rare methotrexate complication, and has only been described in case reports and case series.
OBJECTIVE OBJECTIVE
To document patient characteristics, morphologic features, and mortality risk factors for methotrexate cutaneous ulceration.
METHODS METHODS
A systematic literature review of PubMed and Embase (last date 1 November 2021) was performed with data collected from case reports and case series. This study was limited to cases of cutaneous ulceration; presence of oral ulceration was collected from within these cases.
RESULTS RESULTS
114 cases (men = 57.9%, mean age = 61 years) of methotrexate cutaneous ulceration met inclusion criteria. Psoriasis (69.3%), rheumatoid arthritis (18.4%), and mycosis fungoides (6.1%) were the most common indications for methotrexate use. Morphologies included erosions localized to psoriatic plaques (33.3%), epidermal necrosis/necrolysis (35.1%), localized ulceration (16.7%), and skin-fold erosions (5.3%). Methotrexate dose preceding toxicity varied greatly; median 20 mg/week, interquartile range 15-40 mg/week, range 5-150 mg/week. Most patients had risk factors for serum toxicity (baseline renal dysfunction = 37.8%, concurrent NSAID use = 28.1%, inadequate folic acid use = 89.1%). Thirty percent of cases involved mistakenly high methotrexate doses. Fourteen patients (12%) died. Absence of folic acid use (69% vs. 100%, p value < 0.001), pancytopenia (33% vs. 86%, p value < 0.001), and renal dysfunction at presentation (47% vs. 92%, p value < 0.001) were associated with increased mortality.
LIMITATIONS CONCLUSIONS
Selection bias present due to abstraction from case reports and case series.
CONCLUSION CONCLUSIONS
Methotrexate cutaneous ulceration is commonly preceded by dosage mistakes, absence of folic acid supplementation, and concurrent use of nephrotoxic medications. Renal impairment, pancytopenia, and absence of folic acid supplementation are key risk factors for mortality from this adverse medication reaction. Providers should regularly monitor methotrexate dosing adherence, drug-drug interactions, and perform routine laboratory evaluation. Index of suspicion for this toxicity should remain high given the varied clinical presentation and high mortality.

Identifiants

pubmed: 35486323
doi: 10.1007/s40257-022-00692-1
pii: 10.1007/s40257-022-00692-1
doi:

Substances chimiques

Folic Acid 935E97BOY8
Methotrexate YL5FZ2Y5U1

Types de publication

Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

449-457

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

Références

Kang S, Amagai M, Bruckner AL, Enk AH, Margolis DJ, McMichael AJ, Orringer JS. Fitzpatrick's dermatology, 9th edition. 2019.
Kremer JM. Toward a better understanding of methotrexate. Arthritis Rheum. 2004;50:1370–82.
doi: 10.1002/art.20278 pubmed: 15146406
Romao VC, Lima A, Bernardes M, CanhaoH FJE. Three decades of low-dose methotrexate in rheumatoid arthritis: can we predict toxicity? Immunol Res. 2014;60:289–310.
doi: 10.1007/s12026-014-8564-6 pubmed: 25391609
Olsen E. The pharmacology of methotrexate. J Am Acad Dermatol. 1991;25(2):306–18.
doi: 10.1016/0190-9622(91)70199-C pubmed: 1918470
Lateef O, Shakoor N, Balk RA. Methotrexate pulmonary toxicity. Expert Opin Drug Saf. 2005;4(4):723–30.
doi: 10.1517/14740338.4.4.723 pubmed: 16011450
Shea B, Swinden MV, Ghogomu ET, et al. Folic acid and folinic acid for reducing side effects in patients receiving methotrexate for rheumatoid arthritis. Cochrane Database Syst Rev. 2013. https://doi.org/10.1002/14651858.CD000951.pub2 .
doi: 10.1002/14651858.CD000951.pub2 pubmed: 23728635 pmcid: 7046011
Kivity S, Zafrir Y, Loebstein R, Pauzner R, Mouallem M, Mayan H. Clinical characteristics and risk factors for low dose methotrexate toxicity: a cohort of 28 patients. Autoimmune Rev. 2014;13:1109–13
doi: 10.1016/j.autrev.2014.08.027
Lewis HA, Nemer KM, Chibnall RJ, Musiek AC. Methotrexate-induced cutaneous ulceration in 3 nonpsoriatic patients:report of a rare side effect. JAAD Case Rep. 2017;3(3):236–9.
doi: 10.1016/j.jdcr.2017.02.002 pubmed: 28443320 pmcid: 5394183
Pearce HP, Wilson BB. Erosion of psoriatic plaques: an early sign of methotrexate toxicity. J Am Acad Dermatol. 1996;35(52):835–8.
doi: 10.1016/S0190-9622(96)90097-3 pubmed: 8912599
Lawrence CM, Dahl MG. Two patterns of skin ulceration induced by methotrexate in patients with psoriasis. J Am Acad Dermatol. 1984;11(6):1059–65.
doi: 10.1016/S0190-9622(84)70259-3 pubmed: 6512051
Kaplan DL, Olsen EA. Erosion of psoriatic plaques after chronic methotrexate administration. Int J Dermatol. 1988;27:59–62.
doi: 10.1111/j.1365-4362.1988.tb02342.x pubmed: 3346128
Ladha MA, Edgerton B, Levy J, et al. Methotrexate-induced cutaneous ulceration and necrosis in chronic atopic dermatitis. JAAD Case Rep. 2020;6(9):864–7.
doi: 10.1016/j.jdcr.2020.02.028 pubmed: 32904188 pmcid: 7452306
Breneman DL, Storer TJ, Breneman JC, Mutasim DF. Methotrexate-induced cutaneous ulceration in patients with erythrodermic mycosis fungoides. Ther Clin Risk Manag. 2008;4(5):1135–41.
doi: 10.2147/TCRM.S1155 pubmed: 19209294 pmcid: 2621414
Del Pozo J, Martínez W, García-Silva J, et al. Cutaneous ulceration as a sign of methotrexate toxicity. Eur J Dermatol. 2001;11:450–2.
pubmed: 11525955
Ben-Amitai D, Hodak E, David M. Cutaneous ulceration: an unusual sign of methotrexate toxicity—first report in a patient without psoriasis. Ann Pharmacother. 1998;32:651–3.
doi: 10.1345/aph.17300 pubmed: 9640483
Berna R, DaSilva D, Xu GX, Baumrin E. Methotrexate-induced cutaneous ulceration without pancytopenia in a patient treated for rheumatoid arthritis. JAAD Case Rep. 2021;13:130–3.
doi: 10.1016/j.jdcr.2021.05.024 pubmed: 34195324 pmcid: 8226389
Kurian A, Haber R. Methotrexate-induced cutaneous ulcers in a nonpsoriatic patient: case report and review of the literature. J Cutan Med Surg. 2011;15(5):275–9.
doi: 10.2310/7750.2011.10078 pubmed: 21962187
Monch S, Zimmo B, El Helou T, Colmegna I. Methotrexate-induced cutaneous erosions. Arthritis Rheumatol. 2016;68(1):254.
doi: 10.1002/art.39409 pubmed: 26314707
Montero LC, Gómez RS, de Quirós JF. Cutaneous ulcerations in a patient with rheumatoid arthritis receiving treatment with methotrexate. J Rheumatol. 2000;27:2290–1.
pubmed: 10990260
Shiver MB, Hall LA, Conner KB, Brown GE, Cheung WL, Wirges ML. Cutaneous erosions: a herald for impending pancytopenia in methotrexate toxicity. Dermatol Online J. 2014;20(7):5.
doi: 10.5070/D3207023133
Tekur VK. Methotrexate-induced nonhealing cutaneous ulcers in a nonpsoriatic patient without pancytopenia. Indian Dermatol Online J. 2016;7(5):418–20.
doi: 10.4103/2229-5178.190509 pubmed: 27730043 pmcid: 5038108
Chen TJ, Chung WH, Chen CB, et al. Methotrexate-induced epidermal necrosis: a case series of 24 patients. J Am Acad Dermatol. 2017;77(2):247–55.
doi: 10.1016/j.jaad.2017.02.021 pubmed: 28499754
Yelamos O, Catala A, Vilarrasa E, Roe E, Puig L. Acute severe methotrexate toxicity in patients with psoriasis: a case series and discussion. Dermatology. 2014;229:306–9.
doi: 10.1159/000366501 pubmed: 25401478
Jariwala P, Kumar V, Kothari K, Thakkar S, Umrigar DD. Acute methotrexate toxicity: a fatal condition in two cases of psoriasis. Case Rep Dermatol Med. 2014. https://doi.org/10.1155/2014/946716 .
doi: 10.1155/2014/946716 pubmed: 25276442 pmcid: 4172992
Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systemic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7):e1000097.
doi: 10.1371/journal.pmed.1000097 pubmed: 19621072 pmcid: 2707599
Murad MH, Sultan S, Haffar S, Bazerbachi F. Methodological quality and synthesis of case series and case reports. BMJ Evid Based Med. 2018;23(2):60–3.
doi: 10.1136/bmjebm-2017-110853 pubmed: 29420178 pmcid: 6234235
Agresti A, Caffo B. Simple and effective confidence intervals for proportions and differences of proportions result from adding two successes and two failure. Am Stat. 2000;54(4):280–8.
Wong S, Chong YT, Thevarajah S, et al. Methotrexate toxicity presenting as ulcerated psoriatic plaques. Australas J Dermatol. 2012;53:81–3.
doi: 10.1111/j.1440-0960.2011.00779.x pubmed: 22309341
Lim AY, Gaffney K, Scott DG. Methotrexate-induced pancytopenia: serious and under-reported? Our experience of 25 cases in 5 years. Rheumatology. 2005;44:1051–5
doi: 10.1093/rheumatology/keh685 pubmed: 15901903
Chu E, Allegra C. Antifolates. In: Chabner BA, Longo DL, editors. Cancer chemotherapy and biotherapy. 2nd ed. Philadelphia: Lippincot-Raven; 1996. p. 109–47.
Bleyer WA. The clinical pharmacology of methotrexate: new applications of an old drug. Cancer. 1978;41(1):36–51.
doi: 10.1002/1097-0142(197801)41:1<36::AID-CNCR2820410108>3.0.CO;2-I pubmed: 342086
Howard SC, McCormick J, Pui CH, Buddington RK, Harvey RD. Preventing and managing toxicities of high-dose methotrexate. Oncologist. 2016;21(12):1471–82.
doi: 10.1634/theoncologist.2015-0164 pubmed: 27496039 pmcid: 5153332

Auteurs

Ronald Berna (R)

Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Boulevard, South Tower, 7th floor, Philadelphia, PA, 19104, USA.

Misha Rosenbach (M)

Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Boulevard, South Tower, 7th floor, Philadelphia, PA, 19104, USA.

David J Margolis (DJ)

Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Boulevard, South Tower, 7th floor, Philadelphia, PA, 19104, USA.
Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Nandita Mitra (N)

Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Boulevard, South Tower, 7th floor, Philadelphia, PA, 19104, USA.
Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Emily Baumrin (E)

Department of Dermatology, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Boulevard, South Tower, 7th floor, Philadelphia, PA, 19104, USA. Emily.Baumrin@Pennmedicine.upenn.edu.

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