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Methotrexate versus ciclosporin in the treatment of severe atopic eczema in children: an economic evaluation

Methotrexate versus ciclosporin in the treatment of severe atopic eczema in children: an economic evaluation
Methotrexate versus ciclosporin in the treatment of severe atopic eczema in children: an economic evaluation
Background: eczema (also known as atopic dermatitis) affects 20% of United Kingdom children, with 16% experiencing moderate-to-severe eczema. Eczema impacts patients’ quality of life, mainly through intense itching and sleep disturbance. Most caregivers are able to control their children’s eczema with topical treatments, including emollients, topical corticosteroids or calcineurin inhibitors. For those who do not respond to these topical treatments, or who require consistent use of high potency topical corticosteroids to maintain control, systemic therapies should be considered. Ciclosporin is the most commonly used systemic treatment for paediatric patients, but methotrexate is a widely used promising alternative. Currently, there is not enough evidence to inform guidance about which treatment (methotrexate or ciclosporin) should be used to treat severe atopic eczema in children and young people.

Aim: in this study, we sought to compare the cost-effectiveness of two oral drug treatments (methotrexate or ciclosporin) for children and young people who have severe eczema.

Methods: we collected information on resource use and health-related quality of life using data from the TREAT trial. One hundred and three children and young people aged 2–16 years were randomly allocated to receive either oral methotrexate or ciclosporin for a 36-week treatment period with 24 weeks of further follow-up. An economic evaluation was undertaken, as it is currently uncertain which drug represents the best value for money for the United Kingdom National Health Service. The base case consists of a cost–utility analysis undertaken from a partial National Health Service perspective (limited to medication plus adverse event resource use for which complete data were available from clinical report forms) over 60 weeks; and multiple imputation was used to account for the missing utility data, and the analysis adjusted for baseline cost/utility/Objective Scoring Atopic Dermatitis (as appropriate), gender, age and recruiting centre.

Results: in the base-case analysis, usage of methotrexate resulted not only in cost savings compared to ciclosporin of −£489.67 (95% confidence interval −£685.78 to −£293.36) per participant but also in a small decrease in quality-adjusted life-years of −0.0057 (95% confidence interval −0.0384 to 0.0270) per participant; the resulting net monetary benefit at a willingness to pay per quality-adjusted life-year threshold of £20,000 (£30,000) was £375.49 (£38.45). The probability of methotrexate being cost-effective was 85.5% (73.1%) for a £20,000 (£30,000) threshold. The results were similar in unadjusted analyses and those analyses taking a wider perspective. However, in the secondary cost-effectiveness analysis, methotrexate was found to dominate ciclosporin as it was both cost saving and resulted in a greater improvement in severity scores.

Limitations
Both wider National Health Service resource use (collected by patient diary) and utility data had missing data, which was taken account of using multiple imputation assuming data was missing at random. Being a within-trial economic evaluation, the long-term cost-effectiveness beyond 60 weeks cannot be inferred from this data set or analysis.

Conclusion and future work: this study extends the findings of the TREAT trial by demonstrating that methotrexate and ciclosporin are similar in terms of costs (for visits/monitoring, adverse events and concomitant medications) and quality-adjusted life-years but that methotrexate drug costs are significantly cheaper than ciclosporin drug costs. This supports the conclusion reached in the randomised controlled trial paper that, where first-line novel systemic biologics and small molecules prescribing is generally restricted by health-funding bodies, as is the case in most jurisdictions, methotrexate provides an effective and low-cost, first-line systemic agent and is thus an alternative to ciclosporin. Given its overall cost-effectiveness, methotrexate now needs to be directly compared with novel systemic therapies.
2050-4365
Sach, Tracey H.
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Jones, Ashley
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Rosala-Hallas, Anna
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Spowart, Catherine
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Ashoor, Farhiya
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Irvine, Alan
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Beattie, Paula
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Baron, Susannah
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Browne, Fiona
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Wan, Mandy
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Ahmed, Amina
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Flohr, Carsten
e9cf511f-b1bc-47d1-82ee-28cd8ab0fc56
the TREAT trial Investigator team, on behalf of
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Sach, Tracey H.
5c09256f-ebed-4d14-853a-181f6c92d6f2
Jones, Ashley
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Rosala-Hallas, Anna
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Spowart, Catherine
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Ashoor, Farhiya
663e19d2-ced3-4227-96ac-5ce177121ca7
Irvine, Alan
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Beattie, Paula
93d2b721-effa-4767-bc40-7d234e7bf95a
Baron, Susannah
451fd894-69c7-44e8-96af-b48e11e4fc71
Browne, Fiona
168975ea-148f-46e1-9342-727948fb8788
Wan, Mandy
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Ahmed, Amina
b193d9a0-c848-4901-9103-d09bd9d651d5
Flohr, Carsten
e9cf511f-b1bc-47d1-82ee-28cd8ab0fc56
the TREAT trial Investigator team, on behalf of
343525de-8cc7-4e8f-99e8-8a472740f2e1

Sach, Tracey H., Jones, Ashley, Rosala-Hallas, Anna, Spowart, Catherine, Ashoor, Farhiya, Irvine, Alan, Beattie, Paula, Baron, Susannah, Browne, Fiona, Wan, Mandy, Ahmed, Amina, Flohr, Carsten and the TREAT trial Investigator team, on behalf of (2025) Methotrexate versus ciclosporin in the treatment of severe atopic eczema in children: an economic evaluation. Efficacy and Mechanism Evaluation. (doi:10.3310/GJCF0407).

Record type: Article

Abstract

Background: eczema (also known as atopic dermatitis) affects 20% of United Kingdom children, with 16% experiencing moderate-to-severe eczema. Eczema impacts patients’ quality of life, mainly through intense itching and sleep disturbance. Most caregivers are able to control their children’s eczema with topical treatments, including emollients, topical corticosteroids or calcineurin inhibitors. For those who do not respond to these topical treatments, or who require consistent use of high potency topical corticosteroids to maintain control, systemic therapies should be considered. Ciclosporin is the most commonly used systemic treatment for paediatric patients, but methotrexate is a widely used promising alternative. Currently, there is not enough evidence to inform guidance about which treatment (methotrexate or ciclosporin) should be used to treat severe atopic eczema in children and young people.

Aim: in this study, we sought to compare the cost-effectiveness of two oral drug treatments (methotrexate or ciclosporin) for children and young people who have severe eczema.

Methods: we collected information on resource use and health-related quality of life using data from the TREAT trial. One hundred and three children and young people aged 2–16 years were randomly allocated to receive either oral methotrexate or ciclosporin for a 36-week treatment period with 24 weeks of further follow-up. An economic evaluation was undertaken, as it is currently uncertain which drug represents the best value for money for the United Kingdom National Health Service. The base case consists of a cost–utility analysis undertaken from a partial National Health Service perspective (limited to medication plus adverse event resource use for which complete data were available from clinical report forms) over 60 weeks; and multiple imputation was used to account for the missing utility data, and the analysis adjusted for baseline cost/utility/Objective Scoring Atopic Dermatitis (as appropriate), gender, age and recruiting centre.

Results: in the base-case analysis, usage of methotrexate resulted not only in cost savings compared to ciclosporin of −£489.67 (95% confidence interval −£685.78 to −£293.36) per participant but also in a small decrease in quality-adjusted life-years of −0.0057 (95% confidence interval −0.0384 to 0.0270) per participant; the resulting net monetary benefit at a willingness to pay per quality-adjusted life-year threshold of £20,000 (£30,000) was £375.49 (£38.45). The probability of methotrexate being cost-effective was 85.5% (73.1%) for a £20,000 (£30,000) threshold. The results were similar in unadjusted analyses and those analyses taking a wider perspective. However, in the secondary cost-effectiveness analysis, methotrexate was found to dominate ciclosporin as it was both cost saving and resulted in a greater improvement in severity scores.

Limitations
Both wider National Health Service resource use (collected by patient diary) and utility data had missing data, which was taken account of using multiple imputation assuming data was missing at random. Being a within-trial economic evaluation, the long-term cost-effectiveness beyond 60 weeks cannot be inferred from this data set or analysis.

Conclusion and future work: this study extends the findings of the TREAT trial by demonstrating that methotrexate and ciclosporin are similar in terms of costs (for visits/monitoring, adverse events and concomitant medications) and quality-adjusted life-years but that methotrexate drug costs are significantly cheaper than ciclosporin drug costs. This supports the conclusion reached in the randomised controlled trial paper that, where first-line novel systemic biologics and small molecules prescribing is generally restricted by health-funding bodies, as is the case in most jurisdictions, methotrexate provides an effective and low-cost, first-line systemic agent and is thus an alternative to ciclosporin. Given its overall cost-effectiveness, methotrexate now needs to be directly compared with novel systemic therapies.

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e-pub ahead of print date: 22 October 2025

Identifiers

Local EPrints ID: 506942
URI: http://eprints.soton.ac.uk/id/eprint/506942
ISSN: 2050-4365
PURE UUID: 63093c9e-8544-4890-bfc5-00280648c5d0
ORCID for Tracey H. Sach: ORCID iD orcid.org/0000-0002-8098-9220

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Date deposited: 21 Nov 2025 17:58
Last modified: 22 Nov 2025 03:10

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Contributors

Author: Tracey H. Sach ORCID iD
Author: Ashley Jones
Author: Anna Rosala-Hallas
Author: Catherine Spowart
Author: Farhiya Ashoor
Author: Alan Irvine
Author: Paula Beattie
Author: Susannah Baron
Author: Fiona Browne
Author: Mandy Wan
Author: Amina Ahmed
Author: Carsten Flohr
Author: on behalf of the TREAT trial Investigator team

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