The role of methotrexate TDM in psoriasis treatment
Authors:
J. Chládek
Authors‘ workplace:
Ústav farmakologie, LF UK v Hradci Králové
Published in:
Kardiol Rev Int Med 2015, 17(1): 92-95
Category:
Internal Medicine
Overview
Methotrexate (MTX) is a conventional immunosuppressive drug of first choice in oral therapy of moderate‑ to‑ severe plaque psoriasis. Its use is comfortable and cost effective. The therapy improves the skin status according to the PASI score (psoriasis area and severity index) by 50% or more in up to 75% of patients. However, a high inter‑ individual variability in pharmacokinetics is one of the major factors responsible for either insufficient efficacy of the therapy or its premature discontinuation due to adverse effects of MTX. The review article critically evaluates the possible benefits of therapeutic drug monitoring (TDM) of MTX as a tool for personalized pharmacotherapy of psoriasis. Prospective clinical studies unraveled a relationship between the pharmacokinetics and the therapeutic effect of MTX. Recommendations on how to perform TDM were worked out and verified, which helped to improve the outcomes of the initial treatment phase (remission induction). Besides the individualization of MTX dosing, supplementation with folic acid was individually tailored only to patients with a proven folate deficit.
Keywords:
methotrexate – psoriasis – therapeutic drug monitoring
Sources
1. Grim J, Chládek J, Martínková J. Pharmacokinetics and pharmacodynamics of methotrexate in non‑neoplastic diseases. Clin Pharmacokinet 2003; 42: 139– 151.
2. van Roon EN, van de Laar MA. Methotrexate bioavailability. Clin Exp Rheumatol 2010; 28 (Suppl 5): S27– S32.
3. de Beaumais TA, Jacqz‑ Aigrain E. Intracellular disposition of methotrexate in acute lymphoblastic leukemia in children. Curr Drug Metab 2012; 13: 822– 834.
4. Matherly LH, Wilson MR, Hou Z. The major facilitative folate transporters solute carrier 19A1 and solute carrier 46A1: biology and role in antifolate chemotherapy of cancer. Drug Metab Dispos 2014; 42: 632– 649. doi: 10.1124/ dmd.113.055723.
5. Visentin M, Zhao R, Goldman ID. The antifolates. Hematol Oncol Clin North Am 2012; 26: 629– 648. doi: 10.1016/ j.hoc.2012.02.002.
6. Petros WP, Evans WE. Anticancer drugs. In: Burton ME, Evans WE, Shaw LM et al (eds). Applied pharmacokinetics and pharmacodynamics: principles of therapeutic drug monitoring, Baltimore, Philadelphia: Lippincott Williams & Wilkins 2005: 617– 632.
7. Shen S, O'Brien T, Yap LM et al. The use of methotrexate in dermatology: a review. Australas J Dermatol 2012; 5: 1– 18. doi: 10.1111/ j.1440‑ 0960.2011.00839.x.
8. Griffiths CE, Barker JN. Pathogenesis and clinical features of psoriasis. Lancet 2007; 370: 263– 271.
9. Chladek J, Grim J, Martinkova J et al. Low‑dose methotrexate pharmacokinetics and pharmacodynamics in the therapy of severe psoriasis. Basic Clin Pharmacol Toxicol 2005; 96: 247– 248.
10. Hroch M, Chladek J, Simkova M et al. A pilot study of pharmacokinetically guided dosing of oral methotrexate in the initial phase of psoriasis treatment. J Eur Acad Dermatol Venereol 2008; 22: 19– 24.
11. Chládek J, Simková M, Vanecková J et al. The effect of folic acid supplementation on the pharmacokinetics and pharmacodynamics of oral methotrexate during the remission‑ induction period of treatment for moderate‑ to‑ severe plaque psoriasis. Eur J Clin Pharmacol 2008; 64: 347– 355.
12. Pathirana D, Ormerod AD, Saiag P et al. European S3– guidelines on the systemic treatment of psoriasis vulgaris. J Eur Acad Dermatol Venereol 2009; 23 (Suppl 2): 1– 70. doi: 10.1111/ j.1468‑ 3083.2009.03389.x.
13. Prey P, Paul C. Effect of folic or folinic acid supplementation on methotrexate‑associated safety and efficacy in inflammatory disease: a systematic review. Br J Dermatol 2009; 160: 622– 628. doi: 10.1111/ j.1365‑ 2133.2008.08876.x.
14. Salim A, Tan E, Ilchyshyn A et al. Folic acid supplementation during treatment of psoriasis with methotrexate: a randomized, double‑blind, placebo‑ controlled trial. Br J Dermatol 2006; 154: 1169– 1174.
15. Chládek J, Šimková M, Vaněčková J et al. Individualizovaná farmakoterapie ložiskové psoriázy perorálním metotrexátem: fikce nebo reálná možnost? Československá dermatologie 2012; 87: 221– 228.
16. Gyulai R, Bagot M, Griffiths CE et al. Current practice of methotrexate use for psoriasis: results of a worldwide survey among dermatologists. J Eur Acad Dermatol Venereol 2014; 29: 224– 231. doi: 10.1111/ jdv.12495.
17. Heydendael VM, Spuls PI, Opmeer BC et al. Methotrexate versus cyclosporine in moderate‑ to‑ severe chronic plaque psoriasis Methotrexate versus cyclosporine in moderate‑ to‑ severe chronic plaque psoriasis. N Engl J Med 2003; 349: 658– 665.
18. Flytström I, Stenberg B, Svensson A et al. Methotrexate vs. ciclosporin in psoriasis: effectiveness, quality of life and safety. A randomized controlled trial. Br J Dermatol 2008; 158: 116– 121.
19. Saurat JH, Stingl G, Dubertret L et al. Efficacy and safety results from the randomized controlled comparative study of adalimumab vs. methotrexate vs. placebo in patients with psoriasis (CHAMPION). Br J Dermatol 2008; 158: 558– 566.
20. Barker J, Hoffmann M, Wozel G et al. Efficacy and safety of infliximab vs. methotrexate in patients with moderate‑ to‑ severe plaque psoriasis: results of an open‑ label, active‑ controlled, randomized trial (RESTORE1). Br J Dermatol 2011; 165: 1109– 1117. doi: 10.1111/ j.1365‑ 2133.2011.10615.x.
21. Reich K, Langley RG, Papp KA et al. A 52‑week trial comparing briakinumab with methotrexate in patients with psoriasis. N Engl J Med 2011; 365: 1586– 1596. doi: 10.1056/ NEJMoa1010858.
22. Fallah Arani S, Neumann H, Hop WC et al. Fumarates vs. methotrexate in moderate to severe chronic plaque psoriasis: a multicentre prospective randomized controlled clinical trial. Br J Dermatol 2011; 164: 855– 861. doi: 10.1111/ j.1365‑ 2133.2010.10195.x.
23. Akhyani M, Chams‑ Davatchi C, Hemami MR et al. Efficacy and safety of mycophenolate mofetil vs. methotrexate for the treatment of chronic plaque psoriasis. J Eur Acad Dermatol Venereol 2010; 24: 1447– 1451. doi: 10.1111/ j.1468‑ 3083.2010.03667.x.
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Paediatric cardiology Internal medicine Cardiac surgery CardiologyArticle was published in
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