A comparison of oral methylprednisolone plus azathioprine or mycophenolate mofetil for the treatment of pemphigus

被引:120
作者
Beissert, Stefan
Werfel, Thomas
Frieling, Uta
Boehm, Markus
Sticherling, Michael
Stadler, Rudolf
Zillikens, Detlev
Rzany, Berthold
Hunzelmann, Nicolas
Meurer, Michael
Gollnick, Harald
Ruzicka, Thomas
Pillekamp, Hans
Junghans, Volker
Luger, Thomas A.
机构
[1] Univ Munster, Dept Dermatol, D-48149 Munster, Germany
[2] Hannover Med Sch, D-3000 Hannover, Germany
[3] Univ Kiel, Kiel, Germany
[4] Univ Leipzig, D-7010 Leipzig, Germany
[5] Municipal Hosp Minden, Minden, Germany
[6] Univ Wurzburg, Wurzburg, Germany
[7] Univ Lubeck, Lubeck, Germany
[8] Univ Heidelberg, Fac Clin Med Mannheim, D-6800 Mannheim, Germany
[9] Univ Cologne, Cologne, Germany
[10] Univ Dresden, Dresden, Germany
[11] Univ Magdeburg, D-39106 Magdeburg, Germany
[12] Univ Dusseldorf, D-4000 Dusseldorf, Germany
[13] Univ Ulm, Ulm, Germany
[14] Univ Gottingen, D-3400 Gottingen, Germany
[15] Charite Univ Med Berlin, Dept Dermatol, Div Evidenced Based Med, Berlin, Germany
关键词
D O I
10.1001/archderm.142.11.1447
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Objective: To investigate the safety and efficacy of oral methylprednisolone combined with azathioprine sodium or mycophenolate mofetil for the treatment of pemphigus. Design: A prospective, multicenter, randomized, non-blinded clinical trial to compare 2 parallel groups of patients with pemphigus (pemphigus vulgaris and pemphigus foliaceus) treated with oral methylprednisolone plus azathioprine or oral methylprednisolone plus mycophenolate mofetil. Settings: Thirteen departments of dermatology in Germany. Patients: We included patients with pemphigus vulgaris (n = 33) or pemphigus foliaceus (n = 7) evidenced by clinical lesions suggestive of pemphigus, intraepidermal blistering on histological analysis of skin biopsy specimens, intercellular deposition of IgG within the epidermis, and immunoblot analysis findings for antidesmoglein 3 and/or antidesmoglein 1 autoantibodies. Main Outcome Measures: The cumulative total methylprednisolone doses and rate of remission. Secondary outcome measures were safety profiles and duration of remission. Results: In 13 (72%) of 18 patients with pemphigus receiving oral methylprednisolone and azathioprine, complete remission was achieved after a mean +/- SD of 74 +/- 127 days compared with 20 (95%) of 21 patients receiving oral methylprednisolone and mycophenolate mofetil in whom complete remission occurred after a mean SD of 91 +/- 113 days. The total median cumulative methylprednisolone dose used was 8916 mg (SD, +/-29 844 mg) in the azathioprine group compared with 9334 mg (SD, +/- 13 280 mg) in the mycophenolate group. In 6 (33%) of 18 patients treated with azathioprine, grade 3 or 4 adverse effects were documented in contrast to 4 (19%) of 21 patients who received mycophenolate mofetil. Conclusion: mycophenolate mofetil and azathioprine demonstrate similar efficacy, corticosteroid-sparing effects, and safety profiles as adjuvants during treatment of pemphigus vulgaris and pemphigus foliaceus.
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页码:1447 / 1454
页数:8
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