Skip to main content
. Author manuscript; available in PMC: 2012 Jun 1.
Published in final edited form as: Inflamm Bowel Dis. 2010 Nov 4;17(6):1423–1427. doi: 10.1002/ibd.21484

Table 2.

Association of Recent and Persistent* Immunosuppressive Medication Combinations with Non-Melanoma Skin Cancer Among Patients with Crohn’s Disease

Recent Use (≤90 days) Cases (n=387) Controls (n=1548) OR (95% CI)^ p value
None 250 (65%) 1331 (86%) 1.0 (reference)
Any immunomodulator** 101 (26%) 158 (10%) 3.71 (2.74–5.02) <0.001
Any biologic 14 (4%) 36 (2%) 2.47 (1.29–4.73) 0.006
Combined immunomodulator and biologic 22 (6%) 23 (1%) 5.85 (3.2–10.8) <0.001

Persistent Use (> 365 days) Cases (n=228) Controls (n=913) OR (95% CI)^ p value

None 154 (68%) 817 (89%) 1.0 (reference)
Any immunomodulator** 56 (25%) 73 (8%) 4.45 (2.94–6.75) <0.001
Any biologic 7 (3%) 13 (1%) 3.23 (1.24–8.45) 0.017
Combined immunomodulator and biologic 11 (5%) 10 (1%) 6.75 (2.74–16.65) <0.001
*

Only those with >365 days of exposure time prior to NMSC or index date were included in analyses of persistent medication use

^

ORs and 95% CI by multiple variable conditional logistic regression adjusting for Medicaid insurance status

**

Thiopurine class, calcineurin inhibitor, mycophenolate mofetil, methotrexate

Adalimumab or infliximab

Reproduced with permission from Clinical Gastroenterology and Hepatology12