Sirolimus Use and Cancer Incidence Among US Kidney Transplant Recipients

被引:53
作者
Yanik, E. L. [1 ]
Gustafson, S. K. [2 ]
Kasiske, B. L. [2 ,3 ]
Israni, A. K. [2 ,3 ]
Snyder, J. J. [2 ,3 ]
Hess, G. P. [4 ,5 ]
Engels, E. A. [1 ]
Segev, D. L. [2 ,6 ]
机构
[1] NCI, Div Canc Epidemiol & Genet, Rockville, MD 20852 USA
[2] Minneapolis Med Res Fdn Inc, Sci Registry Transplant Recipients, Minneapolis, MN USA
[3] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[4] Univ Penn, Inst Hlth Econ, Philadelphia, PA 19104 USA
[5] Symphony Hlth Solut, Horsham, PA USA
[6] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
关键词
Cancer; malignancy; neoplasia; clinical research; practice; epidemiology; health services and outcomes research; hematology; oncology; immunosuppressant; immunosuppression; immune modulation; kidney transplantation; nephrology; mechanistic target of rapamycin: sirolimus; RENAL-ALLOGRAFT RECIPIENTS; NONMELANOMA SKIN-CANCER; MAMMALIAN TARGET; CELL CARCINOMA; RAPAMYCIN PATHWAY; TRIAL; INHIBITOR; RISK; TRANSFORMATION; MALIGNANCIES;
D O I
10.1111/ajt.12969
中图分类号
R61 [外科手术学];
学科分类号
摘要
Sirolimus has anti-carcinogenic properties and can be included in maintenance immunosuppressive therapy following kidney transplantation. We investigated sirolimus effects on cancer incidence among kidney recipients. The US transplant registry was linked with 15 population-based cancer registries and national pharmacy claims. Recipients contributed sirolimus-exposed time when sirolimus claims were filled, and unexposed time when other immunosuppressant claims were filled without sirolimus. Cox regression was used to estimate associations with overall and specific cancer incidence, excluding nonmelanoma skin cancers (not captured in cancer registries). We included 32604 kidney transplants (5687 sirolimus-exposed). Overall, cancer incidence was suggestively lower during sirolimus use (hazard ratio [HR]=0.88, 95% confidence interval [CI]=0.70-1.11). Prostate cancer incidence was higher during sirolimus use (HR=1.86, 95% CI=1.15-3.02). Incidence of other cancers was similar or lower with sirolimus use, with a 26% decrease overall (HR=0.74, 95% CI=0.57-0.96, excluding prostate cancer). Results were similar after adjustment for demographic and clinical characteristics. This modest association does not provide strong evidence that sirolimus prevents posttransplant cancer, but it may be advantageous among kidney recipients with high cancer risk. Increased prostate cancer diagnoses may result from sirolimus effects on screen detection. Using a linkage of the US transplant registry with cancer registries and national pharmacy claims, this study finds that sirolimus use after kidney transplantation was associated with a modest decrease in non-prostate cancer incidence.
引用
收藏
页码:129 / 136
页数:8
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