Chen Jenny H C, Wong Germaine, Chapman Jeremy R, Lim Wai H
Department of Renal Medicine, Prince of Wales Hospital, Sydney, Australia.
Centre for Transplant and Renal Research, Westmead Hospital, Sydney, Australia.
PLoS One. 2015 Nov 10;10(11):e0139479. doi: 10.1371/journal.pone.0139479. eCollection 2015.
T-cell depleting antibody is associated with an increased risk of cancer after kidney transplantation, but a dose-dependent relationship has not been established. This study aimed to determine the association between cumulative doses of T-cell depleting antibody and the risk of cancer after kidney transplantation. Using data from the Australian and New Zealand Dialysis and Transplant Registry between 1997-2012, we assessed the risk of incident cancer and cumulative doses of T-cell depleting antibody using adjusted Cox regression models. Of the 503 kidney transplant recipients with 2835 person-years of follow-up, 276 (55%), 209 (41%) and 18 (4%) patients received T-cell depleting antibody for induction, rejection or induction and rejection respectively. The overall cancer incidence rate was 1,118 cancers per 100,000 patient-years, with 975, 1093 and 1377 cancers per 100,000 patient-years among those who had received 1-5 doses, 6-10 doses and >10 doses, respectively. There was no association between cumulative doses of T cell depleting antibody and risk of incident cancer (1-5: referent, 6-10: adjusted hazard ratio (HR) 1.19, 95%CI 0.48-2.95, >10: HR 1.42, 95%CI 0.50-4.02, p = 0.801). This lack of association is contradictory to our hypothesis and is likely attributed to the low event rates resulting in insufficient power to detect significant differences.
T细胞清除抗体与肾移植后癌症风险增加相关,但尚未确立剂量依赖关系。本研究旨在确定T细胞清除抗体的累积剂量与肾移植后癌症风险之间的关联。利用1997年至2012年澳大利亚和新西兰透析与移植登记处的数据,我们使用校正后的Cox回归模型评估了新发癌症风险和T细胞清除抗体的累积剂量。在503例接受肾移植且有2835人年随访的受者中,分别有276例(55%)、209例(41%)和18例(4%)患者接受T细胞清除抗体用于诱导、抗排斥或诱导及抗排斥治疗。总体癌症发病率为每100,000患者年1118例癌症,在接受1 - 5剂、6 - 10剂和>10剂的患者中,每100,000患者年的癌症发病率分别为975例、1093例和1377例。T细胞清除抗体的累积剂量与新发癌症风险之间无关联(1 - 5剂:参照组,6 - 10剂:校正风险比 [HR] 1.19,95%置信区间 [CI] 0.48 - 2.95,>10剂:HR 1.42,95%CI 0.50 - 4.02,p = 0.801)。这种缺乏关联的情况与我们的假设相矛盾,可能归因于事件发生率低,导致检测显著差异的效能不足。