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首页> 外文期刊>Renal failure. >The impact of switching to mTOR inhibitor-based immunosuppression on long-term non-melanoma skin cancer incidence and renal function in kidney and liver transplant recipients
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The impact of switching to mTOR inhibitor-based immunosuppression on long-term non-melanoma skin cancer incidence and renal function in kidney and liver transplant recipients

机译:切换到MTOR抑制剂的免疫抑制对肾脏和肝移植受者的长期非黑色素瘤皮肤癌发病率和肾功能的影响

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Background: Solid organ transplantation is associated with increased risk of non-melanoma skin cancer. Studies with short follow up times have suggested a reduced occurrence of these cancers in recipients treated with mammalian target of rapamycin inhibitors as maintenance immunosuppression. We aimed to describe the occurrence of skin cancers in renal and liver transplant recipients switched from calcineurin inhibitor to sirolimus-based regimes. Methods: We performed a retrospective study of sirolimus conversion within the Irish national kidney and liver transplant programs. These data were linked with the National Cancer Registry Ireland to determine the incidence of NMSC among these recipients. The incidence rate ratio (IRR) for post versus pre-conversion NMSC rates are referred in this study as an effect size with [95% confidence interval]. Results: Of 4,536 kidney transplants and 574 liver transplants functioning on the 1 January 1994 or transplanted between 1 January 1994 and 01 January 1994 and 01 January 2015, 85 kidney and 88 liver transplant recipients were transitioned to sirolimus-based immunosuppression. In renal transplants, the rate of NMSC was 131 per 1000 patient years pre-switch to sirolimus, and 68 per 1000 patient years post switch, with adjusted effect size of 0.48 [0.31???0.74] (p?=?.001) following the switch. For liver transplant recipients, the rate of NMSC was 64 per 1,000 patient years pre-switch and 30 per 1,000 patient years post switch, with an adjusted effect size of 0.49 [0.22???1.09] (p .081). Kidney transplant recipients were followed up for a median 3.4?years. Liver transplants were followed for a median 6.6?years. Conclusions: In this study, the conversion of maintenance immunosuppression from calcineurin inhibitors to mTOR inhibitors for clinical indications did appear to reduce the incidence of NMSC in kidney and liver transplant recipients.
机译:背景:固体器官移植与非黑色素瘤皮肤癌的风险增加有关。短暂的研究表明,用哺乳动物抑制剂的哺乳动物靶标作为维持免疫抑制剂治疗的受试者中,这些癌症的发生降低了。我们的目标是描述从钙素抑制剂转换为西罗莫司的肾脏和肝移植受者的皮肤癌的发生。方法:我们对爱尔兰国家肾脏和肝移植计划中的西罗莫司转化进行了回顾性研究。这些数据与国家癌症登记册爱尔兰联系起来,以确定这些受体中NMSC的发病率。术后与转化前NMSC率的发病率比(IRR)称为效果大小,具有[95%置信区间]。结果:1994年1月1日至1994年1月1日至1994年1月1日和2015年1月1日之间移植的4,536次肝脏移植,85例,85肾和88例肝脏移植受者转移至基于西罗莫司的免疫抑制。在肾移植中,NMSC的速率为每1000岁患者患者预先切换到西罗莫司,每1000例患者较数患者开关68次,调节效果大小为0.48 [0.31≤0.74](p?= 001)跟随开关。对于肝移植受者,NMSC的速率为每1000岁患者年前开关,每1,000岁患者多年后开关30次,调节效果大小为0.49 [0.22≤1.09](p .081)。肾移植接受者随访3.4岁。肝脏移植术后中位6.6岁。结论:在本研究中,从钙碱抑制剂对临床适应症的MTOR抑制剂的维持免疫抑制剂转化似乎降低了肾脏和肝移植受者的NMSC发病率。

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