Furuya Y, Jayarajan S N, Taghavi S, Cordova F C, Patel N, Shiose A, Leotta E, Criner G J, Guy T S, Wheatley G H, Kaiser L R, Toyoda Y
Division of Pulmonary & Critical Care, Department of Medicine, Washington University in St. Louis School of Medicine, St. Louis, MO.
Department of Surgery, Section of Vascular Surgery, Washington University in St. Louis School of Medicine, St. Louis, MO.
Am J Transplant. 2016 Aug;16(8):2334-41. doi: 10.1111/ajt.13739. Epub 2016 May 23.
We examined the effect of alemtuzumab and basiliximab induction therapy on patient survival and freedom from bronchiolitis obliterans syndrome (BOS) in double lung transplantation. The United Network for Organ Sharing database was reviewed for adult double lung transplant recipients from 2006 to 2013. The primary outcome was risk-adjusted all-cause mortality. Secondary outcomes included time to BOS. There were 6117 patients were identified, of whom 738 received alemtuzumab, 2804 received basiliximab, and 2575 received no induction. Alemtuzumab recipients had higher lung allocation scores compared with basiliximab and no-induction recipients (41.4 versus 37.9 versus 40.7, p < 0.001) and were more likely to require mechanical ventilation before to transplantation (21.7% versus 6.5% versus 6.2%, p < 0.001). Median survival was longer for alemtuzumab and basiliximab recipients compared with patients who received no induction (2321 versus 2352 versus 1967 days, p = 0.001). Alemtuzumab (hazard ratio 0.80, 95% confidence interval 0.67-0.95, p = 0.009) and basiliximab induction (0.88, 0.80-0.98, p = 0.015) were independently associated with survival on multivariate analysis. At 5 years, alemtuzumab recipients had a lower incidence of BOS (22.7% versus 55.4 versus 55.9%), and its use was independently associated with lower risk of developing BOS on multivariate analysis. While both induction therapies were associated with improved survival, patients who received alemtuzumab had greater median freedom from BOS.
我们研究了阿仑单抗和巴利昔单抗诱导治疗对双肺移植患者生存率及预防闭塞性细支气管炎综合征(BOS)的效果。回顾了器官共享联合网络数据库中2006年至2013年的成年双肺移植受者。主要结局是风险调整后的全因死亡率。次要结局包括发生BOS的时间。共识别出6117例患者,其中738例接受阿仑单抗治疗,2804例接受巴利昔单抗治疗,2575例未接受诱导治疗。与巴利昔单抗和未诱导治疗的受者相比,接受阿仑单抗治疗的受者肺分配评分更高(41.4对37.9对40.7,p<0.001),且更有可能在移植前需要机械通气(21.7%对6.5%对6.2%,p<0.001)。与未接受诱导治疗的患者相比,接受阿仑单抗和巴利昔单抗治疗的受者中位生存期更长(2321天对2352天对1967天,p=0.001)。多因素分析显示,阿仑单抗(风险比0.80,95%置信区间0.67-0.95,p=0.009)和巴利昔单抗诱导治疗(0.88,0.-0.98,p=0.015)与生存率独立相关。在5年时,接受阿仑单抗治疗的受者BOS发生率较低(22.7%对55.4%对55.9%),多因素分析显示其使用与发生BOS的较低风险独立相关。虽然两种诱导治疗均与生存率提高相关,但接受阿仑单抗治疗的患者从BOS中解脱的中位时间更长。