TY - JOUR
T1 - Comparison of the incidence of de novo malignancy in liver or kidney transplant recipients
T2 - Analysis of 2673 consecutive cases in a single center
AU - Shin, M.
AU - Moon, H. H.
AU - Kim, J. M.
AU - Park, J. B.
AU - Kwon, C. H.D.
AU - Kim, S. J.
AU - Joh, J. W.
PY - 2013/10
Y1 - 2013/10
N2 - Purpose An increased incidence of de novo malignancy (dM) is an established complication among solid organ transplant (SOT) recipients compared with the general population. The aims of this study were to describe the incidence and cumulative risk for development of dM among our transplanted population, depending on various clinical and pathologic variables. Methods We retrospectively reviewed the medical records and pathologic data of SOT recipients performed from February 1995 to December 2010. Results Among 2673 consecutive SOT recipients, the dM that developed in 66 (2.5%) patients included, 16 (0.6%; 24.2% of overall dM) lymphoid dM and 50 (1.9%; 75.8% of overall dM) nonlymphoid dM. Cumulative incidence of dM in liver was significantly higher than that in kidney transplant recipients. A significantly higher cumulative incidence of dM was observed among living donor versus deceased donor SOT. Although the more frequent development of lymphoid dM was observed during the first year posttransplantation, the cumulative risk of nonlymphoid dM increased year by year, reaching a substantially higher incidence than that of lymphoid dM beyond 5 years after SOT. Comparing the various immunosuppressive regimens, the cumulative incidence was greater among the group with basiliximab induction. However, the hazard of occurrence was unaffected by whether tacrolimus or cyclosporine was used for maintenance immunosuppression. The increased risk of dM was not dependent on recipient age or gender. Conclusion This study demonstrated distinctive cumulative incidences of dM in different clinical and pathologic settings.
AB - Purpose An increased incidence of de novo malignancy (dM) is an established complication among solid organ transplant (SOT) recipients compared with the general population. The aims of this study were to describe the incidence and cumulative risk for development of dM among our transplanted population, depending on various clinical and pathologic variables. Methods We retrospectively reviewed the medical records and pathologic data of SOT recipients performed from February 1995 to December 2010. Results Among 2673 consecutive SOT recipients, the dM that developed in 66 (2.5%) patients included, 16 (0.6%; 24.2% of overall dM) lymphoid dM and 50 (1.9%; 75.8% of overall dM) nonlymphoid dM. Cumulative incidence of dM in liver was significantly higher than that in kidney transplant recipients. A significantly higher cumulative incidence of dM was observed among living donor versus deceased donor SOT. Although the more frequent development of lymphoid dM was observed during the first year posttransplantation, the cumulative risk of nonlymphoid dM increased year by year, reaching a substantially higher incidence than that of lymphoid dM beyond 5 years after SOT. Comparing the various immunosuppressive regimens, the cumulative incidence was greater among the group with basiliximab induction. However, the hazard of occurrence was unaffected by whether tacrolimus or cyclosporine was used for maintenance immunosuppression. The increased risk of dM was not dependent on recipient age or gender. Conclusion This study demonstrated distinctive cumulative incidences of dM in different clinical and pathologic settings.
UR - https://www.scopus.com/pages/publications/84886257000
U2 - 10.1016/j.transproceed.2013.08.061
DO - 10.1016/j.transproceed.2013.08.061
M3 - Article
C2 - 24157026
AN - SCOPUS:84886257000
SN - 0041-1345
VL - 45
SP - 3019
EP - 3023
JO - Transplantation Proceedings
JF - Transplantation Proceedings
IS - 8
ER -