Table 3.
Biologic therapies for treatment of nail psoriasis.
| Author | Year | n | Intervention | Comparison | Protocol | Results | LoE [16] | 
|---|---|---|---|---|---|---|---|
| Fabroni et al. [55] | 2011 | 48 | Infliximab | — | 5 mg/kg, iv infusion at weeks 0, 2, 6 and every 8 weeks through week 38 | NAPSI-50 is achieved in 85% of patients at week 14, 96% at week 22, 98% at week 38; NAPSI-75 is achieved in 23% of patients at week 14, 65% at week 22, 81% at week 38; NAPSI-90 is achieved in 29% of patients at week 38 | N/A | 
| 
 | |||||||
| Rich et al. [54] | 2008 | 305 | Infliximab | Placebo | 5 mg/kg, iv infusion at weeks 0, 2, 6 and every 8 weeks through week 46 | 26% and 57% improvements in NAPSI scores at weeks 10 and 24 and complete clearance of target nail in 45% of patients at 1 year | A2 | 
| 
 | |||||||
| Rigopoulos et al. [56] | 2008 | 18 | Infliximab | — | 5 mg/kg iv infusion at weeks 0, 2, 6 and every 8 weeks through week 38 | Significant decrease in NAPSI scores (56 at baseline to 30 at week 14, 16 at week 22, 7 at week 30, and 3.3 at week 38) | N/A | 
| 
 | |||||||
| Bianchi et al. [53] | 2005 | 25 | Infliximab | — | 5 mg/kg, iv, at weeks 0, 2, 6, 14, 22 | NAPSI-50 is achieved in all patients at week 14; NAPSI-75 is achieved in all patients at week 22 | N/A | 
| 
 | |||||||
| Leonardi et al. [57] | 2011 | 36 | Adalimumab | Placebo | 80 mg, sc at week 0, 40 mg every other week starting at week 1, through week 16; patients in the placebo group were started to receive active treatment starting at week 16, through week 28 | Significantly higher improvement in NAPSI scores in the treatment arm (50% versus 8%) at week 16; once switched to adalimumab, patients in the initial placebo group improved 38% at week 28, while patients who began the study with adalimumab continued to improve to 54% | N/A | 
| 
 | |||||||
| Van den Bosch et al. [58] | 2010 | 259 | Adalimumab | — | 40 mg, sc, at every other week through week 12 | Mean NAPSI scores are reduced by 44% at week 12 | N/A | 
| 
 | |||||||
| Rigopoulos et al. [59] | 2010 | 21 | Adalimumab | — | 80 mg, sc at week 0, 40 mg every other week starting at week 1, through week 24 | Significant improvement in all patients after 8th injection; fingernail NAPSI decreased from 11 at baseline to 4 at week 24 in patients with just cutaneous psoriasis and from 24 to 10 in patients with psoriatic arthritis | N/A | 
| 
 | |||||||
| Ortonne et al. [60] | 2012 | 69 | Etanercept | Etanercept | 1st group 50 mg weekly for 24 weeks and 2nd group 50 mg twice weekly for the first 12 weeks, 50 mg weekly for the other 12 weeks, sc | Both dose regimens are effective for nail psoriasis and significant improvement in NAPSI scores in both groups at week 24 | N/A | 
| 
 | |||||||
| Luger et al. [61] | 2009 | 564 | Etanercept | — | 25 mg twice weekly for 54 weeks or 50 mg twice weekly for 12 weeks, continued with 25 mg twice weekly in case of relapse, sc | NAPSI scores improved by 29% at week 12, by 51% at week 54, complete resolution in 30% of patients | N/A | 
| 
 | |||||||
| Kavanaugh et al. [62] | 2009 | 287 | Golimumab | Placebo | 50 or 100 mg, sc, every 4 weeks through week 24 | Significant improvements started as early as at week 14: 25% reduction in NAPSI scores in 50 mg group, 43% reduction in 100 mg group at week 14, 33% reduction in 50 mg, and 54% reduction in 100 mg group at week 24 | B | 
| 
 | |||||||
| Körver et al. [63] | 2006 | 8 | Alefacept | — | 15 mg weekly, im, for 12 weeks | 3 patients showed significant improvement, 3 patients unchanged, and 2 patients worsened | N/A | 
| 
 | |||||||
| Parrish et al. [64] | 2006 | 15 | Alefacept | — | 15 mg weekly, im, for 12 weeks | 39% reduction in NAPSI scores at week 24 | N/A | 
| 
 | |||||||
| Cassetty et al. [65] | 2005 | 6 | Alefacept | — | 15 mg weekly, im, for 12 weeks | 3 patients showed ≥30% improvement in NAPSI scores, 1 unchanged, and 2 worsened | N/A | 
| 
 | |||||||
| Patsatsi et al. [66] | 2013 | 27 | Ustekinumab | — | 45 mg, sc, at weeks 0, 4 and every 12 weeks thereafter (90 mg if patient weight > 100 kg) | Significant improvements in NAPSI scores (43% at week 16, 86% at week 28, and 100% at week 40) | N/A | 
| 
 | |||||||
| Vitiello et al. [67] | 2013 | 13 | Ustekinumab | — | 90 mg (n = 5, patients weight > 100 kg), sc, at weeks 0, 4 and every 12 weeks thereafter or 45 mg in combination with MTX (n = 6) or CsA (n = 2) | 38% reduction in NAPSI scores in monotherapy group, 27% reduction in MTX combination, complete resolution in CsA combination group, at week 12 | N/A | 
| 
 | |||||||
| Igarashi et al. [68] | 2012 | 102 | Ustekinumab | Placebo | 45 or 90 mg, sc, at weeks 0, 4 and every 12 weeks through 72 weeks, placebo group with crossover to ustekinumab at week 12 | Improvement in NAPSI scores: 57% in 45 mg group, 68% in 90 mg group at week 64 | A2 | 
| 
 | |||||||
| Reich et al. [69] | 2011 | 317 | Briakinumab | MTX | Briakinumab 200 mg at weeks 0 and 4, 100 mg every 4 weeks through week 48, sc, MTX 5–25 mg/week for 51 weeks | NAPSI scores of the target fingernail significantly lower with the briakinumab group at weeks 24 and 52, as compared with the methotrexate group | N/A | 
n: number of patients.
sc: subcutaneous.
iv: intravenous.
im: intramuscular.
N/A: not applicable.
NAPSI: nail psoriasis severity index.
MTX: methotrexate.
CsA: cyclosporine.
LoE: level of evidence (A2: randomized, double-blind, controlled trial of good quality, B: randomized controlled trial of poor quality).