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. Author manuscript; available in PMC: 2018 Mar 30.
Published in final edited form as: J Am Acad Dermatol. 2017 Aug 2;77(4):706–712. doi: 10.1016/j.jaad.2017.06.032

Table II.

Multivariate analysis of risk factors for nonmelanoma skin cancer among allogeneic hematopoietic cell transplant recipients

NMSC SCC BCC



Variable Hazard ratio (95% CI) P value Hazard ratio (95% CI) P value Hazard ratio (95% CI) P value
Voriconazole exposure* 1.82 (1.13–2.91) .013 2.25 (1.30–3.89) .004 1.05 (0.44–2.52) .913
Chronic GVHD 1.80 (1.03–3.12) .038 1.88 (0.98–3.62) .058 2.49 (0.89–6.98) .084
Age at HCT 1.07 (1.04–1.10) <.001 1.08 (1.04–1.11) <.001 1.06 (1.02–1.12) .010
Male sex 3.67 (2.00–6.78) <.001 4.34 (2.03–9.26) <.001 2.20 (0.78–6.19) .137
White race 12.60 (3.02–52.52) <.001 15.75 (2.17–114.48) .007 5.85 (0.76–45.18) .090
History of NMSC 10.95 (5.84–20.52) <.001 4.64 (2.31–9.30) <.001 8.35 (2.77–25.16) <.001

BCC, Basal cell carcinoma; CI, confidence interval; GVHD, graft-versus-host disease; HCT, hematopoietic cell transplantation; NMSC, nonmelanoma skin cancer; SD, standard deviation.

*

Voriconazole exposure included both pretransplant and post-transplant exposure.

Voriconazole exposure and diagnosis of chronic GVHD were calculated as time-dependent variables.