2003
DOI: 10.1016/s0303-8467(03)00046-5
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Tacrolimus hydrate (FK506): therapeutic effects and selection of responders in the treatment of myasthenia gravis

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Cited by 22 publications
(11 citation statements)
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“…In addition to synthetic glucocorticoids (GCs), more powerful immunosuppressive drugs including cyclosporine and tacrolimus have been applied to such patients [1][2][3][4][5][6][7]. However, individual variations in the clinical efficacy of immunosuppressive drugs have been observed, and thus the drugs are not always a satisfactory solution for the treatment of patients [8][9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…In addition to synthetic glucocorticoids (GCs), more powerful immunosuppressive drugs including cyclosporine and tacrolimus have been applied to such patients [1][2][3][4][5][6][7]. However, individual variations in the clinical efficacy of immunosuppressive drugs have been observed, and thus the drugs are not always a satisfactory solution for the treatment of patients [8][9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…In such cases tacrolimus is the next candidate drug following the guidelines approved by the Ministry of Public Health, Welfare and Labor of Japan. [2][3][4][5] This agent is classified as an immunosuppressant, which acts as a calcineurin inhibitor, and selectively and reversibly suppresses helper T cells secreting cytokines such as interleukin-2. 6,7 To prospectively investigate therapeutic and harmful effects of tacrolimus, this drug was given to seven refractory patients with MG, including a non-thymectomized one, with or without coadministration of oral prednisolone and anti-cholinesterase agents.…”
Section: Introductionmentioning
confidence: 99%
“…By contrast, no serious adverse events have been associated with tacrolimus treatment of MG for 16 weeks [8,9], 6-32 months [14], 1 year [13], more than 2 years [16], 88-104 weeks [12], or 36 months [17]. Ponseti et al reported 3 patients with solid tumors; however, these events were unlikely to be caused by tacrolimus because of the short interval between start of treatment and diagnosis of malignancy [4].…”
Section: Discussionmentioning
confidence: 99%
“…However, the efficacy and safety of long-term tacrolimus treatment for MG have not been established. There have been several early reports of the effects of tacrolimus, including studies in Japan; however, these studies only evaluated short-term effects, for example over 16 weeks [8,9]. We report here the efficacy and safety of long-term treatment with tacrolimus (5-year follow-up) in 9 patients.…”
Section: Introductionmentioning
confidence: 95%