Literature DB >> 26474779

Optimizing Methotrexate Treatment in Rheumatoid Arthritis: The Case for Subcutaneous Methotrexate Prior to Biologics.

Poonam Sharma1, David G I Scott2.   

Abstract

Methotrexate is the most common disease-modifying antirheumatic drug (DMARD) used in the treatment of rheumatoid arthritis (RA). Current evidence supports its efficacy in the treatment of RA, resulting in improved short-term disease control and long-term outcomes in terms of radiographic progression. Oral methotrexate has traditionally been used first-line due to various reasons, including ease of administration, low cost and easy availability. A methotrexate dose of >15 mg/week is generally required for disease control but oral methotrexate may be only partially effective or poorly tolerated in some patients. The rationale for using subcutaneous (SC) methotrexate is based on its improved bioavailability at higher doses and better tolerability in some patients who have side effects when receiving oral methotrexate. Current guidance advocates 'treating to target', with the aim of inducing remission in RA patients. In some patients, this can be achieved using methotrexate alone or in combination with other traditional DMARDs. Patients who have not responded to two DMARDs, including methotrexate, are eligible for biological therapy as per current National Institute for Health and Care Excellence (NICE) guidance in the UK. Biological treatments are expensive and using SC methotrexate can improve disease control in RA patients, thus potentially avoiding or delaying the requirement for future biological treatment.

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Year:  2015        PMID: 26474779     DOI: 10.1007/s40265-015-0486-7

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  32 in total

1.  Comparison of intramuscular methotrexate and gold sodium thiomalate in the treatment of early erosive rheumatoid arthritis: 12 month data of a double-blind parallel study of 174 patients.

Authors:  R Rau; G Herborn; H Menninger; J Blechschmidt
Journal:  Br J Rheumatol       Date:  1997-03

2.  The comparative effectiveness of oral versus subcutaneous methotrexate for the treatment of early rheumatoid arthritis.

Authors:  Glen S Hazlewood; J Carter Thorne; Janet E Pope; Daming Lin; Diane Tin; Gilles Boire; Boulos Haraoui; Carol A Hitchon; Edward C Keystone; Shahin Jamal; Vivian P Bykerk
Journal:  Ann Rheum Dis       Date:  2015-05-15       Impact factor: 19.103

3.  Pharmacokinetics of low-dose methotrexate in rheumatoid arthritis patients.

Authors:  R A Herman; P Veng-Pedersen; J Hoffman; R Koehnke; D E Furst
Journal:  J Pharm Sci       Date:  1989-02       Impact factor: 3.534

4.  Indispensable or intolerable? Methotrexate in patients with rheumatoid and psoriatic arthritis: a retrospective review of discontinuation rates from a large UK cohort.

Authors:  Elena Nikiphorou; Andra Negoescu; John D Fitzpatrick; Calum T Goudie; Andrew Badcock; Andrew J K Östör; Anshuman P Malaviya
Journal:  Clin Rheumatol       Date:  2014-03-09       Impact factor: 2.980

5.  Canadian Rheumatology Association recommendations for pharmacological management of rheumatoid arthritis with traditional and biologic disease-modifying antirheumatic drugs.

Authors:  Vivian P Bykerk; Pooneh Akhavan; Glen S Hazlewood; Orit Schieir; Anne Dooley; Boulos Haraoui; Majed Khraishi; Sharon A Leclercq; Jean Légaré; Diane P Mosher; James Pencharz; Janet E Pope; John Thomson; Carter Thorne; Michel Zummer; Claire Bombardier
Journal:  J Rheumatol       Date:  2011-09-15       Impact factor: 4.666

6.  Comparison of serum concentrations of methotrexate after various routes of administration.

Authors:  M Freeman-Narrod; B J Gerstley; P F Engstrom; R S Bornstein
Journal:  Cancer       Date:  1975-11       Impact factor: 6.860

7.  Reversal of the antiinflammatory effects of methotrexate by the nonselective adenosine receptor antagonists theophylline and caffeine: evidence that the antiinflammatory effects of methotrexate are mediated via multiple adenosine receptors in rat adjuvant arthritis.

Authors:  M C Montesinos; J S Yap; A Desai; I Posadas; C T McCrary; B N Cronstein
Journal:  Arthritis Rheum       Date:  2000-03

8.  Are switches from oral to subcutaneous methotrexate or addition of ciclosporin to methotrexate useful steps in a tight control treatment strategy for rheumatoid arthritis? A post hoc analysis of the CAMERA study.

Authors:  M F Bakker; J W G Jacobs; P M J Welsing; J H van der Werf; S P Linn-Rasker; M J van der Veen; F P J G Lafeber; J W J Bijlsma
Journal:  Ann Rheum Dis       Date:  2010-05-28       Impact factor: 19.103

9.  Historical perspective on the use of methotrexate for the treatment of rheumatoid arthritis.

Authors:  J R Ward
Journal:  J Rheumatol Suppl       Date:  1985-12

10.  Head-to-head, randomised, crossover study of oral versus subcutaneous methotrexate in patients with rheumatoid arthritis: drug-exposure limitations of oral methotrexate at doses ≥15 mg may be overcome with subcutaneous administration.

Authors:  Michael H Schiff; Jonathan S Jaffe; Bruce Freundlich
Journal:  Ann Rheum Dis       Date:  2014-04-12       Impact factor: 19.103

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  3 in total

1.  Comparing Healthcare Costs Associated with Oral and Subcutaneous Methotrexate or Biologic Therapy for Rheumatoid Arthritis in the United States.

Authors:  Joseph Lee; Ryan Pelkey; Julieanna Gubitosa; Michael F Henrick; Michael L Ganz
Journal:  Am Health Drug Benefits       Date:  2017-02

2.  Size-dependent adsorption performance of ZnO nanoclusters for drug delivery applications.

Authors:  Mustafa Kurban; İskender Muz
Journal:  Struct Chem       Date:  2022-09-30       Impact factor: 1.795

Review 3.  Update on subcutaneous methotrexate for inflammatory arthritis and psoriasis.

Authors:  Gino Antonio Vena; Nicoletta Cassano; Florenzo Iannone
Journal:  Ther Clin Risk Manag       Date:  2018-01-09       Impact factor: 2.423

  3 in total

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