A comparison of oral methylprednisolone plus azathioprine or mycophenolate mofetil for the treatment of pemphigus
| Autor: | Thomas Ruzicka, Markus Böhm, Michael Sticherling, Uta Frieling, Thomas Werfel, Detlef Zillikens, Gisela Bonsmann, Nicolas Hunzelmann, Rudolf Stadler, Thomas A. Luger, Volker Junghans, Berthold Rzany, Michael Meurer, Harald Gollnick, Stefan Beissert, Hans Pillekamp |
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| Rok vydání: | 2006 |
| Předmět: |
Male
medicine.medical_specialty Pemphigoid Anti-Inflammatory Agents Administration Oral Azathioprine Dermatology Mycophenolate Gastroenterology Methylprednisolone Severity of Illness Index Mycophenolic acid Disease-Free Survival IMP Dehydrogenase Internal medicine Germany medicine Humans Prospective Studies integumentary system business.industry Pemphigus vulgaris General Medicine Middle Aged Mycophenolic Acid medicine.disease Surgery Azathioprine sodium Treatment Outcome Drug Therapy Combination Female Bullous pemphigoid business Immunosuppressive Agents Pemphigus medicine.drug |
| Zdroj: | Archives of dermatology. 142(11) |
| ISSN: | 0003-987X |
| Popis: | Objective To investigate the safety and efficacy of oral methylprednisolone combined with azathioprine sodium or mycophenolate mofetil for the treatment of bullous pemphigoid. Design A prospective, multicenter, randomized, nonblinded clinical trial to compare 2 parallel groups of patients with bullous pemphigoid undergoing different treatments. Setting Thirteen departments of dermatology in Germany. Patients Patients with bullous pemphigoid (n = 73) as evidenced by clinical lesions suggestive of bullous pemphigoid, signs of subepidermal blistering on histologic analysis of skin biopsy specimens, linear deposition of IgG and C3 along the dermoepidermal junction, and deposition of autoantibodies at the blister roof in split-skin analysis. Interventions Treatment with oral methylprednisolone plus azathioprine (azathioprine group) or oral methylprednisolone plus mycophenolate mofetil (mycophenolate mofetil group). Main Outcome Measures The cumulative total methylprednisolone doses and rates of remission. Secondary outcome measures were safety profiles and duration of remission. Results In 38 of 38 patients in the azathioprine group (100%), complete remission was achieved after a mean ± SD of 23.8 ± 18.9 days vs 42.0 ± 55.3 days for 35 of 35 patients in the mycophenolate mofetil group (100%). In the azathioprine group, the median ± SD total cumulative methylprednisolone dose used was 4967.0 ± 12 190.7 mg vs 5754.0 ± 9692.8 mg in the mycophenolate mofetil group. Nine of 38 patients in the azathioprine group (24%) experienced grade 3 or 4 adverse effects vs 6 of 35 patients in the mycophenolate mofetil group (17%). Azathioprine therapy induced significantly elevated liver function test results compared with mycophenolate mofetil ( P P = .03), alanine aminotransferase ( P = .03), and γ-glutamyltransferase ( P = .01) than did those in the mycophenolate mofetil group. Conclusions Mycophenolate mofetil or azathioprine demonstrate similar efficacy during treatment of bullous pemphigoid, and similar cumulative corticosteroid doses were given in both treatment arms to control disease. However, mycophenolate mofetil showed a significantly lower liver toxicity profile than azathioprine therapy. Trial Registration clinicaltrials.gov Identifier:NCT00431119 |
| Databáze: | OpenAIRE |
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