Abstract

The risk of cutaneous squamous cell carcinoma (CSCC) is found to be substantially increased after organ transplantation. The association with specific immunosuppressive regimens has been previously investigated, but results are not concordant. We aimed to clarify the relationship between separate immunosuppressive drugs, drug load, timing and risk of post-transplant CSCC. A population-based nested case-control study was performed in the Swedish organ transplantation cohort (n = 5931). All patients who developed CSCC during the follow-up (1970-97) were eligible as cases (n = 207). Controls (n = 189) were randomly selected from the cohort and individually matched to the cases on follow-up time, age at and calendar period of transplantation. Exposure information was collected through extensive and standardized review of medical records. The median time to CSCC was 6.7 years. Post-transplant azathioprine (Aza) treatment considerably increased the risk of CSCC during all time periods analysed, and the risk augmented with increasing dose and duration. Patients who after the entire follow-up period had received a high accumulated dose of Aza had an 8.8-fold increased risk of CSCC in multivariate analysis (P < 0.0001), compared to patients never treated with Aza. Additionally, a high accumulated dose of corticosteroids during the same period conferred a 3.9-fold elevated risk of CSCC (P = 0.09), compared to the lowest accumulated dose of corticosteroids. Cyclosporine treatment was not associated with the risk of CSCC post-transplantation. This study provides evidence that Aza treatment, but not cyclosporine treatment, is strongly associated with post-transplant CSCC risk. The results suggest that the risk of CSCC after organ transplantation is not only an effect of the immunosuppressive load per se.

Highlights

  • With improved survival after organ transplantation, the long-term complications have become evident, such as the increased risk of malignancies

  • The results suggest that the risk of cutaneous squamous cell carcinoma (CSCC) after organ transplantation is an effect of the immunosuppressive load per se

  • All Cs medications were standardized to the corresponding prednisolone dose, CsA microemulsion was standardized to CsA and orally administered drugs were transformed to correspond to 100% bioavailability [24]

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Summary

Introduction

With improved survival after organ transplantation, the long-term complications have become evident, such as the increased risk of malignancies. It has been shown repeatedly that the risk of CSCC increases with time after the transplantation. Compared to the general population, in which sun exposure is a well-known risk factor for CSCC, studies have detected an up to 250-fold increased risk in organ transplant patients [2,5,6,7]. The risk of cutaneous squamous cell carcinoma (CSCC) is found to be substantially increased after organ transplantation. We aimed to clarify the relationship between separate immunosuppressive drugs, drug load, timing and risk of post-transplant CSCC. This study provides evidence that Aza treatment, but not cyclosporine treatment, is strongly associated with post-transplant CSCC risk. The results suggest that the risk of CSCC after organ transplantation is an effect of the immunosuppressive load per se

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