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. 2009 Jun 30;52(9):1732–1744. doi: 10.1007/s00125-009-1418-4

Table 4.

Sensitivity analyses: HRs (95% CIs) for insulin analogues (reference group: human insulin) for malignant neoplasms

Description Dose (IU) Aspart Lispro Glargine
Skin cancer (C44) not treated as a neoplasm (n = 127,031) p = 0.01a p = 0.04a p < 0.0001a
10 0.91 (0.75–1.11) 0.88 (0.73–1.07) 0.91 (0.83–0.99)
30 0.95 (0.79–1.15) 0.94 (0.79–1.12) 1.03 (0.94–1.12)
50 0.99 (0.83–1.19) 1.00 (0.85–1.19) 1.16 (1.06–1.27)
Precancerous lesions and in situ carcinoma (D00–D09) not treated as a neoplasm (n = 127,031) p = 0.84a p = 0.91a p < 0.0001a
10 1.04 (0.86–1.25) 0.97 (0.80–1.17) 1.05 (0.96–1.15)
30 1.03 (0.86–1.24) 0.98 (0.82–1.16) 1.14 (1.05–1.24)
50 1.02 (0.86–1.22) 0.99 (0.84–1.17) 1.24 (1.14–1.35)
Oral glucose-lowering agents stratified into subclasses (biguanides, sulfonylureas, α-glucosidase inhibitors, glitazones, other oral glucose-lowering agents) (n = 127,031) p = 0.84a p = 0.90a p < 0.0001a
10 1.05 (0.87–1.26) 0.96 (0,79–1.16) 1.09 (1.00–1.19)
30 1.04 (0.87–1.25) 0.97 (0.82–1.15) 1.18 (1.08–1.28)
50 1.03 (0.87–1.23) 0.98 (0.83–1.15) 1.27 (1.17–1.39)
Biguanides (yes/no) as an additional covariate (n = 127,031) p = 0.83a p = 0.91a p < 0.0001a
10 1.05 (0.87–1.26) 0.96 (0.79–1.16) 1.07 (0.98–1.17)
30 1.04 (0.87–1.24) 0.97 (0.82–1.15) 1.16 (1.07–1.27)
50 1.03 (0.86–1.23) 0.98 (0.83–1.16) 1.26 (1.16–1.37)
Patients with a follow-up time of at least 1.5 yearsb (n = 69,766) p = 0.06a p = 0.05a p < 0.0001a
10 0.90 (0.71–1.15) 1.18 (0.91–1.52) 1.06 (0.96–1.18)
30 0.97 (0.78–1.20) 0.98 (0.82–1.18) 1.13 (1.02–1.25)
50 1.03 (0.84–1.28) 0.82 (0.66–1.02) 1.20 (1.08–1.33)
Patients prescribed oral glucose-lowering agents (n = 101,389) p = 0.60a p = 0.91a p < 0.0001a
10 1.07 (0.87–1.31) 0.95 (0.75–1.20) 1.04 (0.95–1.15)
30 1.05 (0.86–1.29) 0.96 (0.78–1.18) 1.18 (1.08–1.29)
50 1.04 (0.85–1.26) 0.96 (0.79–1.18) 1.33 (1.21–1.46)

Sensitivity analyses are based on an adjusted model including age, sex, dose and interaction terms of insulin group and dose as covariates. Because of the dose-dependent effect size, the adjusted HRs are shown for three dose levels

ap values refer to a simultaneous test of main effects and all corresponding interaction effects

bTime between study entry and study end