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. 2019 Apr 17;17(5):503–516. doi: 10.1111/ddg.13834

Table 3.

Treatment outcomes and reasons for discontinuation

ACI MTX FAE CyA ALI APR ADA ETA INX GOL CER UST SEC
Total number of treatment courses, n 205 220 96 70 53 35 69 62 32 12 8 42 31
Non‐responsea, n (%) 66 (32.2) 82 (37.3) 36 (37.5) 8 (11.4) 20 (37.7) 9 (25.7) 19 (27.5) 16 (25.8) 7 (21.9) 3 (25.0) 0 (0.0) 7 (16.7) 11 (35.5)
Partial responsea, n (%) 87 (42.4) 78 (35.5) 34 (35.4) 23 (32.9) 19 (35.9) 10 (28.6) 23 (33.3) 33 (53.2) 12 (37.5) 4 (33.3) 3 (37.5) 16 (38.1) 8 (25.8)
Excellent responsea, n (%) 40 (19.5) 37 (16.8) 17 (17.7) 36 (51.4) 12 (22.6) 11 (31.4) 23 (33.3) 12 (19.4) 13 (40.6) 5 (41.7) 5 (62.5) 13 (31.0) 9 (29.0)
Treatment discontinued, n (%) 156 (76.1) 175 (79.6) 80 (83.3) 60 (85.7) 39 (73.6) 14 (40.0) 47 (68.1) 52 (83.9) 20 (62.5) 6 (50.0) 1 (12.5) 21 (50.0) 18 (58.1)
▸Adverse eventsb, n (%) 93 (59.6) 72 (41.1) 55 (68.8) 28 (46.7) 11 (28.2) 4 (28.6) 18 (38.3) 11 (21.2) 9 (45.0) 1 (16.7) 1 (100) 3 (14.3) 2 (11.1)
▸Ineffectiveness skinb, n (%) 83 (53.2) 96 (54.9) 28 (35.0) 14 (23.3) 29 (74.4) 8 (57.1) 30 (63.8) 36 (69.2) 11 (55.0) 3 (50.0) 1 (100) 14 (66.7) 12 (66.7)
▸Ineffectiveness jointsb, n (%) 9 (5.8) 30 (17.1) 2 (2.5) 1 (1.7) 0 (0.0) 2 (14.3) 16 (34.0) 22 (42.3) 3 (15.0) 5 (83.3) 1 (100) 9 (42.9) 2 (11.1)
▸Remissionb, n (%) 5 (3.2) 7 (4.0) 7 (8.8) 9 (15.0) 6 (15.4) 0 (0.0) 0 (0.0) 1 (1.9) 0 (0.0) 0 (0.0) 0 (0.0) 1 (4.8) 0 (0.0)
a

Response was evaluated at the end of treatment or time of last observation according to physician's description and/or photographic evidence.

b

Percentage of all patients who discontinued the respective treatment. Multiple reasvons could be stated.

Abbr.: ACI, acitretin; MTX, methotrexate; FAE, fumaric acid esters; CyA, cyclosporine A; ALI, alitretinoin; APR, apremilast; ADA, adalimumab; ETA, etanercept; INX, infliximab; GOL, golimumab; CER, certolizumab pegol; UST, ustekinumab; SEC, secukinumab.