Review Article
The Tumor Necrosis Factor Superfamily of Cytokines in the Inflammatory Myopathies: Potential Targets for Therapy
Table 1
Tumor necrosis factor inhibitors for treating inflammatory myopathies: published trial results for infliximab and etanercept.
| Compound and treatment regimen | Diagnosis/patients continued to end point | Follow-up time | Clinical outcome at end point | Reference |
| infliximab 6 mg/kg 4-weekly or more frequent | R-JDM/5 | 32 to 130 weeks | I (5/5) | [19] | infliximab 10 mg/kg (week 0, 2, 6, 14) | R-DM/1 R-PM/4 R-IBM/4 | 16 weeks | NC (1/1) I (2/4) W (2/4) I (1/4) NC (3/4) | [20] | infliximab 10 mg/kg (week 0, 2, 4) | R-DM/1 R-PM/1 | 12 weeks | I (1/1) I (1/1) | [21] | infliximab 10 mg/kg (week 20) infliximab 10 mg/kg (week 14, 18, 22) | R-DM/1 R-PM/1 | 66 weeks | I (1/1) I (1/1) | [22] | infliximab 10 mg/kg (week 0, 2, 6, 14, 22) | PM/2 | 26 weeks | I (2/2) | [23] | infliximab 8 mg/kg (week 0, 2, 6) | R-DM/1 | 6 weeks | I (1/1) | | infliximab 10 mg/kg (week 0, 2, 4, 6, 9) | R-PM/1 | 69 weeks | I (1/1) | [24] | infliximab 3 mg/kg (week 0, 2, 6, every 8) and etanercept 25 mg twice weekly | R-DM/1 R-PM/2 | 36 to 96 weeks | PR (1/1) I (2/2) | [25] | etanercept 25 mg twice weekly | R-DM/1 | 56 weeks | I (1/1) | [26] |
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Abbreviations: dermatomyositis (DM), improved (I), inclusion body myositis (IBM), juvenile DM (JDM), no change (NC), partial response (PR), polymyositis (PM), refractory DM/PM/IBM (R-DM/PM/IBM), worsened (W).
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