Table 2

Summary of AEs of interest reported for CZP-treated patients (all doses) in the combined RCT and OLE periods (RCT+OLE)

Overall (n=11 317;
21 695 PY)
RA (n=6927;
13 542 PY)
axSpA (n=315;
978 PY)
PsA (n=393;
1316 PY)
PSO (n=1112;
1481 PY)
CD (n=2570;
4378 PY)
Mean exposure (years)1.921.953.103.351.331.70
Median exposure (years)1.151.133.753.991.510.86
IR/100 PY[n (%)]
SIEs*3.62
[757 (6.7)]
3.44
[450 (6.5)]
1.67
[16 (5.1)]
1.64
[21 (5.3)]
1.50
[22 (2.0)]
5.97
[248 (9.6)]
OIs including TB disease0.39
[85 (0.8)]
0.51
[69 (1.0)]
0.10
[1 (0.3)]
0.08
[1 (0.3)]
0.14
[2 (0.2)]
0.27
[12 (0.5)]
 All TB disease0.29
[62 (0.5)]
0.38
[51 (0.7)]
0.10
[1 (0.3)]
00.14
[2 (0.2)]
0.18
[8 (0.3)]
 TB disease by date of treatment initiation†Pre-20070.42
[50 (1.1)]
0.52
[42 (1.8)]
N/AN/A1.46
[1 (0.9)]
0.19
[7 (0.3)]
2007 onwards0.12
[12 (0.2)]
0.17
[9 (0.2)]
0.10
[1 (0.3)]
00.07
[1 (0.1)]
0.13
[1 (0.2)]
 Herpes zoster0.06
[14 (0.1)]
0.07
[10 (0.1)]
0.10
[1 (0.3)]
0.08
[1 (0.3)]
00.05
[2 (0.1)]
All malignancies0.82
[178 (1.6)]
0.93
[125 (1.8)]
0.51
[5 (1.6)]
0.46
[6 (1.5)]
0.68
[10 (0.9)]
0.73
[32 (1.2)]
 All malignancies excluding NMSC0.66
[144 (1.3)]
0.77
[104 (1.5)]
0.41
[4 (1.3)]
0.46
[6 (1.5)]
0.47
[7 (0.6)]
0.53
[23 (0.9)]
 Melanoma0.06
[12 (0.1)]
0.06
[8 (0.1)]
0000.09
[4 (0.2)]
 Lymphoma, including Hodgkin’s disease‡0.06
[13 (0.1)]
0.07
[10 (0.1)]
00.08
[1 (0.3)]
0.07
[1 (0.1)]
0.02
[1 (0.0)]
 NMSC0.17
[37 (0.3)]
0.16
[22 (0.3)]
0.10
[1 (0.3)]
00.20
[3 (0.3)]
0.25
[11 (0.4)]
MACE0.47
[101 (0.9)]
0.62
[84 (1.2)]
0.10
[1 (0.3)]
0.54
[7 (1.8)]
0.27
[4 (0.4)]
0.11
[5 (0.2)]
GI perforations0.08
[17 (0.2)]
0.04
[5 (0.1)]
0000.27
[12 (0.5)]
New onset or worsening psoriasis§0.03
[6 (0.1)]
00.10
[1 (0.3)]
00.27
[4 (0.4)]
0.02
[1 (0.0)]
Venous thromboembolism¶0.23
[49 (0.4)]
0.27
[37 (0.5)]
00.31
[4 (1.0)]
0.14
[2 (0.2)]
0.14
[6 (0.2)]
 Pulmonary embolism (SAEs only)0.09
[20 (0.2)]
0.11
[15 (0.2)]
00.23
[3 (0.8)]
0.07
[1 (0.1)]
0.02
[1 (0.0)]
  • n (%) refers to the number of patients with events; zeros indicate that there were no cases. NMSC includes serious and non-serious cases.

  • *Including the five appendicitis events confirmed as SIEs during the previous safety update in RA.18

  • †Before 2007, a positive TB result on the PPD tuberculin skin test varied (from ≥5 to ≥20 mm) according to geographic region. Since 2007, CZP recommendations internationally mandate all patients with PPD ≥5 mm receive treatment for latent TB infection. There were no patients with axSpA or PsA enrolled prior to 2007.

  • ‡Lymphoma cases include two cases of Hodgkin’s disease, one in RA and one in PSO.

  • §Worsening psoriasis defined as psoriasis reported as an AE in a patient enrolled in a PSO study; new-onset psoriasis defined as psoriasis in a patient enrolled in a non-PSO study.

  • ¶Includes serious and non-serious deep vein thrombosis and pulmonary embolism events.

  • AE, adverse event; axSpA, axial spondyloarthritis; CD, Crohn’s disease; CZP, certolizumab pegol; GI, gastrointestinal; IR, incidence rate (the number of new cases per 100 PY, with the denominator being the exposure duration up to the first occurrence of a particular AE); MACE, major adverse cardiovascular events;NMSC, non-melanoma skin cancer;OI, opportunistic infection;OLE, open-label extension; PPD, purified protein derivative; PsA, psoriatic arthritis; PSO, psoriasis; PY, patient-years; RA, rheumatoid arthritis;RCT, randomised controlled trial;SAE, serious adverse event;SIE, serious infectious event;TB, tuberculosis.