A randomized controlled trial protocol assessing the effectiveness, safety and cost‐effectiveness of methotrexate vs. ciclosporin in the treatment of severe atopic eczema in children: the TREatment of severe Atopic eczema Trial (TREAT)4. (28th October 2018)
- Record Type:
- Journal Article
- Title:
- A randomized controlled trial protocol assessing the effectiveness, safety and cost‐effectiveness of methotrexate vs. ciclosporin in the treatment of severe atopic eczema in children: the TREatment of severe Atopic eczema Trial (TREAT)4. (28th October 2018)
- Main Title:
- A randomized controlled trial protocol assessing the effectiveness, safety and cost‐effectiveness of methotrexate vs. ciclosporin in the treatment of severe atopic eczema in children: the TREatment of severe Atopic eczema Trial (TREAT)4
- Authors:
- Irvine, A.D.
Jones, A.P.
Beattie, P.
Baron, S.
Browne, F.
Ashoor, F.
O'Neill, L.
Rosala‐Hallas, A.
Sach, T.
Spowart, C.
Taams, L.
Walker, C.
Wan, M.
Webb, N.
Williamson, P.
Flohr, C. - Other Names:
- Layton Alison investigator.
Burton Tim investigator.
Grainge Michael investigator.
Arden‐Jones Michael investigator.
King Saskia investigator.
Perkin Michael investigator.
Taieb Alain investigator.
Ormerod Anthony investigator.
Chalmers Robert investigator.
Liu Xinxue investigator.
Ahmed Amina investigator.
Ashoor Farhiya investigator.
Rosala‐Hallas Anna investigator.
Holton Amy investigator.
Irvine Alan investigator.
Jones Ashley investigator.
Sach Tracey investigator.
Spowart Catherine investigator.
Wan Mandy investigator.
Walker Charlotte investigator.
Williamson Paula investigator.
August Suzannah investigator.
Beattie Paula investigator.
Brown Sara investigator.
Cork Mike investigator.
Esdaile Ben investigator.
Gach Joanna investigator.
Howard Emma investigator.
McPherson Tess investigator.
O'Kane Donal investigator.
Ravenscroft Jane investigator.
Shaw Lindsay investigator.
Allen Caroline investigator.
Baron Susannah investigator.
Greenblatt Danielle investigator.
Hearn Robert investigator.
Hoey Susannah investigator.
Jarret Rachael investigator.
Jury Catherine investigator.
Mitchell Charlie investigator.
Murphy Ruth investigator.
Ogg Graham investigator.
Plant Alice investigator.
Newell Louise investigator.
Srinivasan Jothsana investigator.
Wedgeworth Emma investigator.
Webb Nicholas investigator.
Taams Leonie investigator.
O'Neil Luke investigator.
Mclean Irwin investigator.
… (more) - Abstract:
- Summary: Background: Oral systemic immunomodulatory medication is regularly used off‐licence in children with severe atopic eczema. However, there is no firm evidence regarding the effectiveness, safety, cost‐effectiveness and impact on quality of life from an adequately powered randomized controlled trial (RCT) using systemic medication in children. Objectives: To assess whether there is a difference in the speed of onset, effectiveness, side‐effect profile and reduction in flares post‐treatment between ciclosporin (CyA) and methotrexate (MTX), and also the cost‐effectiveness of the drugs. Treatment impact on quality of life will also be examined in addition to whether FLG genotype influences treatment response. In addition, the trial studies the immune–metabolic effects of CyA and MTX. Methods: Multicentre, parallel group, assessor‐blind, pragmatic RCT of 36 weeks' duration with a 24‐week follow‐up period. In total, 102 children aged 2–16 years with moderate‐to‐severe atopic eczema, unresponsive to topical treatment will be randomized (1 : 1) to receive MTX (0·4 mg kg −1 per week) or CyA (4 mg kg −1 per day). Results: The trial has two primary outcomes: change from baseline to 12 weeks in Objective Severity Scoring of Atopic Dermatitis (o‐SCORAD) and time to first significant flare following treatment cessation. Conclusions: This trial addresses important therapeutic questions, highlighted in systematic reviews and treatment guidelines for atopic eczema. The trial designSummary: Background: Oral systemic immunomodulatory medication is regularly used off‐licence in children with severe atopic eczema. However, there is no firm evidence regarding the effectiveness, safety, cost‐effectiveness and impact on quality of life from an adequately powered randomized controlled trial (RCT) using systemic medication in children. Objectives: To assess whether there is a difference in the speed of onset, effectiveness, side‐effect profile and reduction in flares post‐treatment between ciclosporin (CyA) and methotrexate (MTX), and also the cost‐effectiveness of the drugs. Treatment impact on quality of life will also be examined in addition to whether FLG genotype influences treatment response. In addition, the trial studies the immune–metabolic effects of CyA and MTX. Methods: Multicentre, parallel group, assessor‐blind, pragmatic RCT of 36 weeks' duration with a 24‐week follow‐up period. In total, 102 children aged 2–16 years with moderate‐to‐severe atopic eczema, unresponsive to topical treatment will be randomized (1 : 1) to receive MTX (0·4 mg kg −1 per week) or CyA (4 mg kg −1 per day). Results: The trial has two primary outcomes: change from baseline to 12 weeks in Objective Severity Scoring of Atopic Dermatitis (o‐SCORAD) and time to first significant flare following treatment cessation. Conclusions: This trial addresses important therapeutic questions, highlighted in systematic reviews and treatment guidelines for atopic eczema. The trial design is pragmatic to reflect current clinical practice. Abstract : What's already known about this topic? Oral systemic immunomodulatory medication is regularly used off‐licence in children with severe atopic eczema. Ciclosporin is the commonest first‐line systemic agent used in this context, but methotrexate has emerged as an important therapeutic alternative. There is currently no adequately powered randomized controlled trial that compares both treatments in children. What does this study add? The TREatment of severe Atopic eczema Trial (TREAT) addresses this gap and compares the effectiveness, safety, cost‐effectiveness and impact on patient's quality of life of these two drugs. TREAT also examines the effects of both drugs using systemic and cutaneous markers of inflammation and the effect of filaggrin ( FLG ) genotype and T‐cell cytokine signatures on treatment response. Respond to this article Plain language summary available online … (more)
- Is Part Of:
- British journal of dermatology. Volume 179:Number 6(2018)
- Journal:
- British journal of dermatology
- Issue:
- Volume 179:Number 6(2018)
- Issue Display:
- Volume 179, Issue 6 (2018)
- Year:
- 2018
- Volume:
- 179
- Issue:
- 6
- Issue Sort Value:
- 2018-0179-0006-0000
- Page Start:
- 1297
- Page End:
- 1306
- Publication Date:
- 2018-10-28
- Subjects:
- Dermatology -- Periodicals
Skin -- Diseases -- Periodicals
616.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2133 ↗
https://academic.oup.com/bjd ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bjd.16717 ↗
- Languages:
- English
- ISSNs:
- 0007-0963
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2307.400000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8864.xml