Mycophenolate mofetil in AChR-antibody-positive myasthenia gravis: outcomes in 102 patients.

Published

Journal Article

Two recent randomized, controlled trials failed to demonstrate a benefit of mycophenolate mofetil (MMF) over prednisone in the treatment of myasthenia gravis (MG). We reviewed our experience with MMF in MG to determine whether these trials may have been unsuccessful because of their short duration and the unpredicted benefit of prednisone. We reviewed outcomes and prednisone dosage for all our acetylcholine-receptor (AChR)-antibody positive MG patients treated with MMF alone or with prednisone for at least 3 months. The percentage of patients with a desirable outcome (MG-specific Manual Muscle Test score <4 or Myasthenia Gravis Foundation of America post-invention status of minimal manifestations or better) began to increase after 6 months; 80% of those followed for >24 months had a desirable outcome. Prednisone dose decreased after 12 months; after 25 months, 54.5% of patients took no prednisone and 75% took <7.5 mg/day. This retrospective analysis provides class IV evidence that MMF begins to improve AChR-positive MG after 6 months, both with prednisone and as monotherapy.

Full Text

Duke Authors

Cited Authors

  • Hehir, MK; Burns, TM; Alpers, J; Conaway, MR; Sawa, M; Sanders, DB

Published Date

  • May 2010

Published In

Volume / Issue

  • 41 / 5

Start / End Page

  • 593 - 598

PubMed ID

  • 20405499

Pubmed Central ID

  • 20405499

Electronic International Standard Serial Number (EISSN)

  • 1097-4598

International Standard Serial Number (ISSN)

  • 0148-639X

Digital Object Identifier (DOI)

  • 10.1002/mus.21640

Language

  • eng