A randomized trial of methotrexate versus azathioprine for severe atopic eczema

Background Patients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as off-label treatment options, but direct comparisons are lacking. Objectives We sought to compare the efficacy and safety of methotrexate versus...

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Published in:Journal of allergy and clinical immunology Vol. 128; no. 2; pp. 353 - 359
Main Authors: Schram, Mandy Elvira, MD, Roekevisch, Evelien, MD, Leeflang, Mariska Maria Geertruida, PhD, Bos, Jan Dositheus, MD, PhD, FRCP, Schmitt, Jochen, MD, Spuls, Phyllis Ira, MD, PhD
Format: Journal Article
Language:English
Published: New York, NY Mosby, Inc 01-08-2011
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Abstract Background Patients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as off-label treatment options, but direct comparisons are lacking. Objectives We sought to compare the efficacy and safety of methotrexate versus azathioprine in adults with severe atopic eczema. Methods Patients with severe atopic eczema were randomly assigned in a 1:1 ratio to receive either methotrexate (dosage, 10-22.5 mg/wk) or azathioprine (dosage, 1.5-2.5 mg/kg/d) for 12 weeks, followed by a 12-week follow-up period. Primary outcome was the mean change in the severity scoring of atopic dermatitis index after 12 weeks. Efficacy assessors blinded for allocation of treatment were used to perform clinical outcome assessment. Analyses were done on an intention-to-treat basis. Results Of the 45 patients screened, 42 were included. At week 12, patients in the methotrexate group had a mean relative reduction in the severity scoring of atopic dermatitis index of 42% (SD, 18%) compared with 39% (SD, 25%) in the azathioprine group ( P  = .52). Proportions of patients achieving at least mild disease and reductions on impact of quality of life, symptoms, and levels of thymus and activation-regulated chemokine were similar in both groups at weeks 12 and 24. No statistically significant differences were found in the number and severity of adverse events. Abnormalities in blood count were more common in the azathioprine group. No serious adverse events occurred. Conclusion Both treatments achieved clinically relevant improvement and were safe in the short term. Methotrexate and azathioprine are appropriate options for the treatment of severe atopic eczema.
AbstractList BACKGROUNDPatients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as off-label treatment options, but direct comparisons are lacking.OBJECTIVESWe sought to compare the efficacy and safety of methotrexate versus azathioprine in adults with severe atopic eczema.METHODSPatients with severe atopic eczema were randomly assigned in a 1:1 ratio to receive either methotrexate (dosage, 10-22.5 mg/wk) or azathioprine (dosage, 1.5-2.5 mg/kg/d) for 12 weeks, followed by a 12-week follow-up period. Primary outcome was the mean change in the severity scoring of atopic dermatitis index after 12 weeks. Efficacy assessors blinded for allocation of treatment were used to perform clinical outcome assessment. Analyses were done on an intention-to-treat basis.RESULTSOf the 45 patients screened, 42 were included. At week 12, patients in the methotrexate group had a mean relative reduction in the severity scoring of atopic dermatitis index of 42% (SD, 18%) compared with 39% (SD, 25%) in the azathioprine group (P = .52). Proportions of patients achieving at least mild disease and reductions on impact of quality of life, symptoms, and levels of thymus and activation-regulated chemokine were similar in both groups at weeks 12 and 24. No statistically significant differences were found in the number and severity of adverse events. Abnormalities in blood count were more common in the azathioprine group. No serious adverse events occurred.CONCLUSIONBoth treatments achieved clinically relevant improvement and were safe in the short term. Methotrexate and azathioprine are appropriate options for the treatment of severe atopic eczema.
Background Patients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as off-label treatment options, but direct comparisons are lacking. Objectives We sought to compare the efficacy and safety of methotrexate versus azathioprine in adults with severe atopic eczema. Methods Patients with severe atopic eczema were randomly assigned in a 1:1 ratio to receive either methotrexate (dosage, 10-22.5 mg/wk) or azathioprine (dosage, 1.5-2.5 mg/kg/d) for 12 weeks, followed by a 12-week follow-up period. Primary outcome was the mean change in the severity scoring of atopic dermatitis index after 12 weeks. Efficacy assessors blinded for allocation of treatment were used to perform clinical outcome assessment. Analyses were done on an intention-to-treat basis. Results Of the 45 patients screened, 42 were included. At week 12, patients in the methotrexate group had a mean relative reduction in the severity scoring of atopic dermatitis index of 42% (SD, 18%) compared with 39% (SD, 25%) in the azathioprine group ( P  = .52). Proportions of patients achieving at least mild disease and reductions on impact of quality of life, symptoms, and levels of thymus and activation-regulated chemokine were similar in both groups at weeks 12 and 24. No statistically significant differences were found in the number and severity of adverse events. Abnormalities in blood count were more common in the azathioprine group. No serious adverse events occurred. Conclusion Both treatments achieved clinically relevant improvement and were safe in the short term. Methotrexate and azathioprine are appropriate options for the treatment of severe atopic eczema.
Patients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as off-label treatment options, but direct comparisons are lacking. We sought to compare the efficacy and safety of methotrexate versus azathioprine in adults with severe atopic eczema. Patients with severe atopic eczema were randomly assigned in a 1:1 ratio to receive either methotrexate (dosage, 10-22.5 mg/wk) or azathioprine (dosage, 1.5-2.5 mg/kg/d) for 12 weeks, followed by a 12-week follow-up period. Primary outcome was the mean change in the severity scoring of atopic dermatitis index after 12 weeks. Efficacy assessors blinded for allocation of treatment were used to perform clinical outcome assessment. Analyses were done on an intention-to-treat basis. Of the 45 patients screened, 42 were included. At week 12, patients in the methotrexate group had a mean relative reduction in the severity scoring of atopic dermatitis index of 42% (SD, 18%) compared with 39% (SD, 25%) in the azathioprine group ( P = .52). Proportions of patients achieving at least mild disease and reductions on impact of quality of life, symptoms, and levels of thymus and activation-regulated chemokine were similar in both groups at weeks 12 and 24. No statistically significant differences were found in the number and severity of adverse events. Abnormalities in blood count were more common in the azathioprine group. No serious adverse events occurred. Both treatments achieved clinically relevant improvement and were safe in the short term. Methotrexate and azathioprine are appropriate options for the treatment of severe atopic eczema.
Patients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as off-label treatment options, but direct comparisons are lacking. We sought to compare the efficacy and safety of methotrexate versus azathioprine in adults with severe atopic eczema. Patients with severe atopic eczema were randomly assigned in a 1:1 ratio to receive either methotrexate (dosage, 10-22.5 mg/wk) or azathioprine (dosage, 1.5-2.5 mg/kg/d) for 12 weeks, followed by a 12-week follow-up period. Primary outcome was the mean change in the severity scoring of atopic dermatitis index after 12 weeks. Efficacy assessors blinded for allocation of treatment were used to perform clinical outcome assessment. Analyses were done on an intention-to-treat basis. Of the 45 patients screened, 42 were included. At week 12, patients in the methotrexate group had a mean relative reduction in the severity scoring of atopic dermatitis index of 42% (SD, 18%) compared with 39% (SD, 25%) in the azathioprine group (P = .52). Proportions of patients achieving at least mild disease and reductions on impact of quality of life, symptoms, and levels of thymus and activation-regulated chemokine were similar in both groups at weeks 12 and 24. No statistically significant differences were found in the number and severity of adverse events. Abnormalities in blood count were more common in the azathioprine group. No serious adverse events occurred. Both treatments achieved clinically relevant improvement and were safe in the short term. Methotrexate and azathioprine are appropriate options for the treatment of severe atopic eczema.
Background Patients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as off-label treatment options, but direct comparisons are lacking. Objectives We sought to compare the efficacy and safety of methotrexate versus azathioprine in adults with severe atopic eczema. Methods Patients with severe atopic eczema were randomly assigned in a 1:1 ratio to receive either methotrexate (dosage, 10-22.5 mg/wk) or azathioprine (dosage, 1.5-2.5 mg/kg/d) for 12 weeks, followed by a 12-week follow-up period. Primary outcome was the mean change in the severity scoring of atopic dermatitis index after 12 weeks. Efficacy assessors blinded for allocation of treatment were used to perform clinical outcome assessment. Analyses were done on an intention-to-treat basis. Results Of the 45 patients screened, 42 were included. At week 12, patients in the methotrexate group had a mean relative reduction in the severity scoring of atopic dermatitis index of 42% (SD, 18%) compared with 39% (SD, 25%) in the azathioprine group (P = .52). Proportions of patients achieving at least mild disease and reductions on impact of quality of life, symptoms, and levels of thymus and activation-regulated chemokine were similar in both groups at weeks 12 and 24. No statistically significant differences were found in the number and severity of adverse events. Abnormalities in blood count were more common in the azathioprine group. No serious adverse events occurred. Conclusion Both treatments achieved clinically relevant improvement and were safe in the short term. Methotrexate and azathioprine are appropriate options for the treatment of severe atopic eczema.
Author Bos, Jan Dositheus, MD, PhD, FRCP
Spuls, Phyllis Ira, MD, PhD
Leeflang, Mariska Maria Geertruida, PhD
Roekevisch, Evelien, MD
Schmitt, Jochen, MD
Schram, Mandy Elvira, MD
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  fullname: Schmitt, Jochen, MD
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  fullname: Spuls, Phyllis Ira, MD, PhD
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https://www.ncbi.nlm.nih.gov/pubmed/21514637$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright American Academy of Allergy, Asthma & Immunology
2011 American Academy of Allergy, Asthma & Immunology
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Copyright © 2011 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.
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ID FETCH-LOGICAL-c610t-f5252f528630ff6067dd1cf1fd5e6963d09e44316dc14c6e615f9d63cec3362f3
ISSN 0091-6749
IngestDate Fri Oct 25 23:12:02 EDT 2024
Fri Oct 25 05:34:34 EDT 2024
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Fri Feb 23 02:26:44 EST 2024
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Issue 2
Keywords SCORAD
IGA
POEM
Severity scoring of atopic dermatitis
Eczema area and intensity index
TPMT
Patient global assessment
atopic dermatitis
azathioprine
methotrexate
VAS
Thymus and activation-regulated chemokine
PGA
Atopic eczema
trial
Thiopurine methyltransferase
Visual analog scale
EASI
Patient-oriented eczema measurement
Investigator global assessment
TARC
off-label
Antineoplastic agent
Allergy
Immunopathology
Skin disease
Thiopurine derivatives
Atopy
Antifolate
Randomization
Immunology
Antimetabolic
Atopic dermatitis
Eczema
Clinical trial
Azathioprine
Methotrexate
Comparative study
Language English
License CC BY 4.0
Copyright © 2011 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.
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Snippet Background Patients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as...
Patients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as off-label...
BACKGROUNDPatients with severe atopic eczema frequently require systemic treatment to control their disease. Methotrexate and azathioprine are proposed as...
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SubjectTerms Adult
Allergic diseases
Allergy and Immunology
atopic dermatitis
Atopic eczema
azathioprine
Azathioprine - administration & dosage
Azathioprine - adverse effects
Azathioprine - therapeutic use
Biological and medical sciences
Children & youth
Clinical medicine
Clinical trials
Dermatitis, Atopic - drug therapy
Dermatitis, Atopic - physiopathology
Disease
Drug dosages
Drug therapy
Eczema
Enzymes
Female
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Immunopathology
Immunosuppressive Agents - administration & dosage
Immunosuppressive Agents - adverse effects
Immunosuppressive Agents - therapeutic use
Male
Medical sciences
methotrexate
Methotrexate - administration & dosage
Methotrexate - adverse effects
Methotrexate - therapeutic use
Middle Aged
off-label
Quality of Life
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Severity of Illness Index
Skin allergic diseases. Stinging insect allergies
Studies
Treatment Outcome
trial
Title A randomized trial of methotrexate versus azathioprine for severe atopic eczema
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https://search.proquest.com/docview/888118564
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