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肺移植后伏立康唑和鳞状细胞癌:一项多中心研究。

Voriconazole and squamous cell carcinoma after lung transplantation: A multicenter study.

机构信息

Department of Pharmacy, University Health Network, Toronto, ON, Canada.

Department of Cardiothoracic, Transplant, and Vascular Surgery, Hannover Medical School, Hannover, Germany.

出版信息

Am J Transplant. 2018 Jan;18(1):113-124. doi: 10.1111/ajt.14500. Epub 2017 Oct 16.

Abstract

This study evaluated the independent contribution of voriconazole to the development of squamous cell carcinoma (SCC) in lung transplant recipients, by attempting to account for important confounding factors, particularly immunosuppression. This international, multicenter, retrospective, cohort study included adult patients who underwent lung transplantation during 2005-2008. Cox regression analysis was used to assess the effects of voriconazole and other azoles, analyzed as time-dependent variables, on the risk of developing biopsy-confirmed SCC. Nine hundred lung transplant recipients were included. Median follow-up time from transplantation to end of follow-up was 3.51 years. In a Cox regression model, exposure to voriconazole alone (adjusted hazard ratio 2.39, 95% confidence interval 1.31-4.37) and exposure to voriconazole and other azole(s) (adjusted hazard ratio 3.45, 95% confidence interval 1.07-11.06) were associated with SCC compared with those unexposed after controlling for important confounders including immunosuppressants. Exposure to voriconazole was associated with increased risk of SCC of the skin in lung transplant recipients. Residual confounding could not be ruled out because of the use of proxy variables to control for some confounders. Benefits of voriconazole use when prescribed to lung transplant recipients should be carefully weighed versus the potential risk of SCC. EU PAS registration number: EUPAS5269.

摘要

本研究通过尝试考虑重要的混杂因素,特别是免疫抑制,评估伏立康唑对肺移植受者鳞状细胞癌(SCC)发展的独立贡献。这项国际、多中心、回顾性队列研究纳入了 2005-2008 年期间接受肺移植的成年患者。使用 Cox 回归分析评估伏立康唑和其他唑类药物(作为时变变量进行分析)对经活检证实的 SCC 发展风险的影响。共纳入 900 例肺移植受者。从移植到随访结束的中位随访时间为 3.51 年。在 Cox 回归模型中,与未暴露组相比,单独暴露于伏立康唑(调整后的危险比 2.39,95%置信区间 1.31-4.37)和暴露于伏立康唑和其他唑类药物(调整后的危险比 3.45,95%置信区间 1.07-11.06)与 SCC 相关,在控制了包括免疫抑制剂在内的重要混杂因素后。暴露于伏立康唑与肺移植受者皮肤 SCC 的风险增加相关。由于使用替代变量来控制一些混杂因素,因此不能排除残留混杂的可能性。在权衡肺移植受者使用伏立康唑的益处与 SCC 的潜在风险时应谨慎。欧盟药品管理局注册号:EUPAS5269。

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