Table 2.
Promising treatments in dermatomyositis
Drug | Type of Study | No. of patients who received treatment | Dose | Concomitant steroid use | Concomitant Steroid sparing agents | Treatment response (%) | Source |
---|---|---|---|---|---|---|---|
Lenabasum | Phase 2 double-blinded, randomized, placebo-controlled | 20 | 20 mg BID | Yes | Yes | 13/18 (72%) achieved low skin disease activity (CDASI ≤ 14) at week 68 | Werth [27, 28] |
Abatacept | Phase 2 randomized, treatment delayed-start trial | 19 | Weight-based dose individuals weighing < 60 kg received 500 mg, those 60–100 kg received 750 mg, and those > 100 kg received 1000 mg. | Yes | Yes | 8/19 (42%) achieved the DOI at 6 months | Tjamlund [29] |
Tofacitinib | Single-center open-label prool-of-concept study | 10 | 11 mg XR daily | Yes | No | 10/10 (100%) met the primary outcome DOI at 12 weeks, with 50% demonstrating moderate improvement and 50% having minimal improvement based on the TIS | Paik [30] |
Rituximab | Randomized placebo-phase--controlled trial (post hoc analyses) | 120 | Based on BSA: children with BSA < 1.5 m2 received 575 mg/m2 per infusion; adults and children with BSA of 1.5 m2 received 750 mg/m2 up to 1 g per infusion | Yes | Yes | The cutaneous visual analog scale activity improved in adult DM (3.22 1.72, p = 0.0002) and JDM (3.26 1.56, p < 0.0001) at 44 weeks | Aggarwal [31] |