Zwart Eline S, Yüksel Esen, Pannekoek Anne, de Vries Ralph, Mebius Reina E, Kazemier Geert
Amsterdam Universities Medical Centers, Cancer Center Amsterdam, Department of Surgery, VU University, 1081 HV Amsterdam, The Netherlands.
Amsterdam Universities Medical Centers, Department of Molecular Cell Biology and Immunology, VU University, 1081 HV Amsterdam, The Netherlands.
Cancers (Basel). 2021 Mar 5;13(5):1122. doi: 10.3390/cancers13051122.
Immunosuppressive therapy after solid organ transplantation leads to the development of cancer in many recipients. Analysis of the occurrence of different types of de novo carcinomas in relation to specific immunosuppressive drugs may give insight into their carcinogenic process and carcinogenesis in general. Therefore, a systematic search was performed in Embase and PubMed. Studies describing over five de novo carcinomas in patients using immunosuppressive drugs after solid organ transplantation were included. Incidence per 1000 person-years was calculated with DerSimonian-Laird random effects model and odds ratio for developing carcinomas with the Mantel-Haenszel test. Following review of 5606 papers by title and abstract, a meta-analysis was conducted of 82 studies. The incidence rate of de novo carcinomas was 8.41. Patients receiving cyclosporine developed more de novo carcinomas compared to tacrolimus (OR1.56, 95%CI 1.00-2.44) and mycophenolate (OR1.26, 95%CI 1.03-1.56). Patients receiving azathioprine had higher odds to develop de novo carcinomas compared to mycophenolate (OR3.34, 95%CI 1.29-8.65) and head and neck carcinoma compared to tacrolimus (OR3.78, 95%CI 1.11-12.83). To conclude, patients receiving immunosuppressive drugs after solid organ transplantation have almost a 20-fold increased likelihood of developing carcinomas, with the highest likelihood for patients receiving cyclosporine A and azathioprine. Looking into altered immune pathways affected by immunosuppressive drugs might lead to better understanding of carcinogenesis in general.
实体器官移植后的免疫抑制治疗会导致许多接受者患癌。分析不同类型的新发癌与特定免疫抑制药物的关系,可能有助于深入了解其致癌过程及总体致癌机制。因此,我们在Embase和PubMed数据库中进行了系统检索。纳入了描述实体器官移植后使用免疫抑制药物的患者中超过5例新发癌的研究。采用DerSimonian-Laird随机效应模型计算每1000人年的发病率,并使用Mantel-Haenszel检验计算患癌的比值比。在通过标题和摘要对5606篇论文进行筛选后,对82项研究进行了荟萃分析。新发癌的发病率为8.41。与接受他克莫司的患者相比,接受环孢素的患者发生更多新发癌(比值比1.56,95%置信区间1.00 - 2.44),与接受霉酚酸酯的患者相比也是如此(比值比1.26,95%置信区间1.03 - 1.56)。与接受霉酚酸酯的患者相比,接受硫唑嘌呤的患者患新发癌的几率更高(比值比3.34,95%置信区间1.29 - 8.65),与接受他克莫司的患者相比,患头颈癌的几率更高(比值比3.78,95%置信区间1.11 - 12.83)。总之,实体器官移植后接受免疫抑制药物治疗的患者患癌可能性增加近20倍,接受环孢素A和硫唑嘌呤的患者可能性最高。研究受免疫抑制药物影响的免疫途径改变,可能有助于更全面地了解致癌机制。