Parameters | OR (95% CI), P value | ||
After 1 year | After 2 years | After 3 years | |
EFT | 2.04 (0.89 to 4.78), 0.09 | 2.19 (1.11 to 4.42), 0.02* | 2.11 (1.03 to 4.44), 0.04* |
Early use of CNIs | 1.59 (0.78 to 3.24), 0.20 | 2.09 (1.09 to 4.06), 0.03* | 2.36 (1.13 to 5.09), 0.02* |
Oral PSL dosing regimen | |||
Low-dose/high-dose | 10.4 (4.54 to 25.2), <0.0001* | 2.75 (1.31 to 5.88), 0.007* | 1.86 (0.79 to 4.49), 0.15 |
Low-dose/intermediate-dose | 13.4 (5.69 to 34.8), <0.0001* | 3.99 (1.86 to 8.81), 0.0003* | 4.92 (2.00 to 12.6), 0.0004* |
The following variables were also entered in the multivariate logistic model: demographics, antibody status, thymus status, pyridostigmine use, MGFA postintervention status, worst QMG score, accumulated dose of HMP, PE/PP and Ig. Factors that did not show significance after being run through the model are not shown.
EFT is use of fast-acting therapy such as PP, often combined with HMP, HMP alone or intravenous Ig within 6 months of treatment initiation.
*An independent predictor to achieve the treatment target.
CNIs, calcineurin inhibitors; EFT, early fast-acting treatment; HMP, high-dose intravenous methylprednisolone; Ig, immunoglobulin; MGFA, Myasthenia Gravis Foundation of America; MM-or-better-5mg for ≥6 months, minimal manifestation status or better on PSL ≤5 mg/day lasting >6 months (the treatment target); PE/PP, plasma exchange/plasmapheresis; PSL, prednisolone; QMG, quantitative myasthenia gravis.