Fox Benjamin Daniel, Ashquar Fadi, Raviv Yael, Rozengarten Dror, Straichman Osnat, Izhakian Shimon, Kramer Mordechai Reuven
Pulmonary Institute, Rabin Medical Center, Petach Tikva, Israel.
Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Ann Transplant. 2017 Nov 14;22:677-681. doi: 10.12659/aot.904417.
BACKGROUND Lung transplant (LTx) recipients suffer from high rates of malignancy. Exposure to immunosuppressive medication such as tacrolimus has been proposed as a risk factor for tumorigenesis. We hypothesized that chronically high levels of tacrolimus would be associated with risk of malignancy. MATERIAL AND METHODS The study was performed in a transplant center in Israel, with a nested case-control design. Cases were LTx recipients who were diagnosed with any solid or hematological malignancy except non-melanoma skin cancer. Controls were tumor-free during their entire follow-up after LTx and had at least the same follow-up time as their matched case. Controls were matched to cases by age and type of transplant received (single/double). Tacrolimus levels were extracted and analyzed for median drug level and also integrated over time (area under the curve - AUC-tacrolimus). RESULTS We reviewed 412 LTx recipients in our registry. Thirty-nine cases of malignancy were diagnosed and 160 controls were matched, giving a crude tumor incidence rate of 26/100 000/year. Lung cancers were the commonest diagnosis. Cases and controls were well matched by age, smoking status, and LTx type. Median tacrolimus levels were 11.0 ng/ml and 11.3 ng/ml in cases and controls, respectively (p=0.88). The median log (AUC-tacrolimus) was 9.4 in the cases and 9.5 in the controls (p=0.59). CONCLUSIONS In this nested case-control study, exposure to tacrolimus was similar in tumor cases and non-tumor controls. These data, based on a cohort with modest size, suggest either that tumorigenesis in LTx recipients is unrelated to tacrolimus exposure or that levels in these patients are above an unknown threshold at which the dose-response effect is saturated.
肺移植(LTx)受者患恶性肿瘤的几率很高。接触诸如他克莫司等免疫抑制药物被认为是肿瘤发生的一个危险因素。我们推测,长期高水平的他克莫司会与患恶性肿瘤的风险相关。
该研究在以色列的一个移植中心进行,采用巢式病例对照设计。病例为被诊断患有任何实体或血液系统恶性肿瘤(非黑色素瘤皮肤癌除外)的LTx受者。对照是LTx术后整个随访期间无肿瘤且随访时间至少与匹配病例相同的受者。对照根据年龄和接受的移植类型(单肺/双肺)与病例进行匹配。提取并分析他克莫司水平,以得出药物中位水平,并计算随时间的积分(曲线下面积 - 他克莫司AUC)。
我们查阅了登记册中的412名LTx受者。诊断出39例恶性肿瘤,并匹配了160名对照,得出的粗肿瘤发病率为26/100 000/年。肺癌是最常见的诊断。病例和对照在年龄、吸烟状况和LTx类型方面匹配良好。病例组和对照组的他克莫司中位水平分别为11.0 ng/ml和11.3 ng/ml(p = 0.88)。病例组的中位log(他克莫司AUC)为9.4,对照组为9.5(p = 0.59)。
在这项巢式病例对照研究中,肿瘤病例和非肿瘤对照接触他克莫司的情况相似。基于规模适中的队列得出的这些数据表明,要么LTx受者的肿瘤发生与接触他克莫司无关,要么这些患者的水平高于一个未知的阈值,在该阈值下剂量反应效应已饱和。