Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by VAN DEN HOOGEN, F. H. J.
Right arrow Articles by VAN DE PUTTE, L. B. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by VAN DEN HOOGEN, F. H. J.
Right arrow Articles by VAN DE PUTTE, L. B. A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1996 British Society for Rheumatology


other

COMPARISON OF METHOTREXATE WITH PLACEBO IN THE TREATMENT OF SYSTEMIC SCLEROSIS: A 24 WEEK RANDOMIZED DOUBLE-BLIND TRIAL, FOLLOWED BY A 24 WEEK OBSERVATIONAL TRIAL

F. H. J. VAN DEN HOOGEN, A. M. T. BOERBOOMS, A. J. G. SWAAK*, J. J. RASKER{dagger}, H. J. J. VAN LIER{ddagger} and L. B. A. VAN DE PUTTE

*Department of Rheumatology, Daniël den Hoedkliniek Rotterdam
{dagger}Department of Rheumatology, Medisch Spectrum Twente Enschede
{ddagger}Department of Medical Statistics, University of Nijmegen Nijmegen, The Netherlands
Department of Rheumatology, University Hospital Nijmegen

Correspondence to: Correspondence to: F. H. J. van den Hoogen, Department of Rheumatology, University Hospital, PO Box 9101, 6500 HB Nijmegen, The Netherlands.

In this study, methotrexate (MTX) was compared with placebo in the treatment of systemic sclerosis (scleroderma, SSc) in a 24 week randomized double-blind trial, followed by an observational trial of 24 weeks duration. Twenty-nine scleroderma patients were allocated to receive weekly injections of either 15 mg MTX or placebo. Patients who responded favourably after 24 weeks continued with the same regimen for a further 24 weeks; those who showed a poor response on placebo were allocated to further treatment with 15 mg MTX weekly, and those who responded poorly to treatment with 15 mg MTX weekly had their doses increased to 25 mg. A favourable response was defined as an improvement of total skin score (TSS) by greater double equals 30%, of single breath diffusion capacity (DLco) by greater double equals 15%, or of the score on a visual analogue scale of general well-being (VAS) by greater double equals 30%, provided that such improvements were not accompanied by persistent digital ulcerations or worsening of DLco greater double equals15%. Seventeen patients were allocated to MTX treatment and 12 to treatment with placebo. After 24 weeks, a significantly larger number of patients receiving MTX (n = 8, 53%) who completed the first 24 weeks of the study had responded favourably compared to patients receiving placebo (n = 1, 10%, P = 0.03). Comparison of separate variables between the two treatment groups by intention-to-treat analysis at week 24 showed improvement in the MTX group of TSS (P = 0.06) and creatinine clearance (P = 0.07). At week 48, 13 patients received MTX from the start of the study and nine during 24 weeks. From these 22 patients, 15 (68%) responded favourably and compared with the start of the study they showed significant improvement of TSS (P = 0.04), VAS (P = 0.02), grip strength of the right hand (P = 0.02) and ESR (P = 0.01). Although the number of patients enrolled in this study is small, these results suggest that in a group of patients with active systemic sclerosis, low-dose MTX seems to be more effective than placebo according to pre-defined response criteria.

KEY WORDS: Systemic sclerosis, Methotrexate, Double-blind placebo-controlled treatment, Side-effects


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Ann Rheum DisHome page
O Kowal-Bielecka, R Landewe, J Avouac, S Chwiesko, I Miniati, L Czirjak, P Clements, C Denton, D Farge, K Fligelstone, et al.
EULAR recommendations for the treatment of systemic sclerosis: a report from the EULAR Scleroderma Trials and Research group (EUSTAR)
Ann Rheum Dis, May 1, 2009; 68(5): 620 - 628.
[Abstract] [Full Text] [PDF]


Home page
The Journal of RheumatologyHome page
S. A. KHUDER and B. KAHALEH
Statistics and the Relationship of Clinical Research to Clinical Practice
J Rheumatol, February 1, 2009; 36(2): 219 - 220.
[Full Text] [PDF]


Home page
The Journal of RheumatologyHome page
S. R. JOHNSON, B. M. FELDMAN, J. E. POPE, and G. A. TOMLINSON
Shifting Our Thinking About Uncommon Disease Trials: The Case of Methotrexate in Scleroderma
J Rheumatol, February 1, 2009; 36(2): 323 - 329.
[Abstract] [Full Text] [PDF]


Home page
Ann Rheum DisHome page
M C Vonk, Z Marjanovic, F H J van den Hoogen, S Zohar, A V M B Schattenberg, W E Fibbe, J Larghero, E Gluckman, F W M B Preijers, A P J van Dijk, et al.
Long-term follow-up results after autologous haematopoietic stem cell transplantation for severe systemic sclerosis
Ann Rheum Dis, January 1, 2008; 67(1): 98 - 104.
[Abstract] [Full Text] [PDF]


Home page
Rheumatology (Oxford)Home page
N. Blank, R. Max, and H.-M. Lorenz
The role of DMARDs in systemic sclerosis therapy
Rheumatology, October 1, 2006; 45(suppl_3): iii42 - iii44.
[Abstract] [Full Text] [PDF]


Home page
Arch DermatolHome page
A. Kreuter, T. Gambichler, F. Breuckmann, S. Rotterdam, M. Freitag, M. Stuecker, K. Hoffmann, and P. Altmeyer
Pulsed High-Dose Corticosteroids Combined With Low-Dose Methotrexate in Severe Localized Scleroderma
Arch Dermatol, July 1, 2005; 141(7): 847 - 852.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
R. K. Burt, S. Slavin, W. H. Burns, and A. M. Marmont
Induction of tolerance in autoimmune diseases by hematopoietic stem cell transplantation: getting closer to a cure?
Blood, February 1, 2002; 99(3): 768 - 784.
[Abstract] [Full Text] [PDF]


Home page
JRSMHome page
H. Dobbie, J. Lanham, and R. Unwin
Morphea presenting as widespread oedema
J R Soc Med, January 9, 2002; 95(9): 459 - 460.
[Full Text] [PDF]


Home page
Arch DermatolHome page
A. N. Sapadin and R. Fleischmajer
Treatment of Scleroderma
Arch Dermatol, January 1, 2002; 138(1): 99 - 105.
[Abstract] [Full Text] [PDF]


Home page
Ann Rheum DisHome page
M Binks, J R Passweg, D Furst, P McSweeney, K Sullivan, C Besenthal, J Finke, H H Peter, J van Laar, F C Breedveld, et al.
Phase I/II trial of autologous stem cell transplantation in systemic sclerosis: procedure related mortality and impact on skin disease
Ann Rheum Dis, June 1, 2001; 60(6): 577 - 584.
[Abstract] [Full Text] [PDF]


Home page
Ann Rheum DisHome page
G Valentini, A Della Rossa, S Bombardieri, W Bencivelli, A J Silman, S D'Angelo, M M. Cerinic, J F Belch, C M Black, P Bruhlmann, et al.
European multicentre study to define disease activity criteria for systemic sclerosis. II. Identification of disease activity variables and development of preliminary activity indexes
Ann Rheum Dis, June 1, 2001; 60(6): 592 - 598.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.