2007
DOI: 10.1111/j.1365-2133.2006.07686.x
|View full text |Cite
|
Sign up to set email alerts
|

An open-label, dose-ranging study of methotrexate for moderate-to-severe adult atopic eczema

Abstract: We have shown that MTX is an effective, well-tolerated treatment for moderate-to-severe atopic eczema, and response appears to compare favourably with other second-line therapies. A randomized, controlled trial is now warranted.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

3
111
0
10

Year Published

2008
2008
2020
2020

Publication Types

Select...
6
3
1

Relationship

0
10

Authors

Journals

citations
Cited by 149 publications
(124 citation statements)
references
References 18 publications
(36 reference statements)
3
111
0
10
Order By: Relevance
“…A retrospective study reported a response in 75% of patients after receiving methotrexate for three months, 14 and a prospective trial confirmed a significant treatment benefit (>50% improvement) for most patients after a similar duration. 15 A recently published RCT compared 12 weeks' treatment with methotrexate or azathioprine in 42 patients. 16 Both showed clinically relevant therapeutic benefit with similar response rates, thereby indicating …”
Section: Methotrexatementioning
confidence: 99%
“…A retrospective study reported a response in 75% of patients after receiving methotrexate for three months, 14 and a prospective trial confirmed a significant treatment benefit (>50% improvement) for most patients after a similar duration. 15 A recently published RCT compared 12 weeks' treatment with methotrexate or azathioprine in 42 patients. 16 Both showed clinically relevant therapeutic benefit with similar response rates, thereby indicating …”
Section: Methotrexatementioning
confidence: 99%
“…A recent open-label, dose-escalating study in 12 adult patients with severe AD demonstrated a 52% improvement in the clinical score over baseline values at week 24, and only 1 patient withdrew from further treatment because of adverse events, a result that is clinically meaningful. 96 By using the same scoring system (six-area, six-sign SD score), azathioprine showed a 37% improvement over baseline values at week 12 (placebo 20%) in a double-blind, placebo-controlled study in patients with moderateto-severe AD older than 16 years, 97 thus confirming efficacy as assessed during an earlier trial. 98 Although adverse events, such as leucopenia and increased liver transaminase levels, need to be carefully monitored, these data indicate that azathioprine is effective in AD.…”
Section: The Role Of Adaptive Immunity In Ad Pathogenesismentioning
confidence: 84%
“…İstenen etki elde edildikten sonra azaltılıp bırakılması önerilmektedir. Psoriazisli çocuk hastalardaki veriler MTX'in çocuklarda güvenilir olduğu yönündedir 125 .…”
Section: Metotreksatunclassified