Leisenring Wendy M, Martin Paul J, Petersdorf Effie W, Regan Anne E, Aboulhosn Nada, Stern Jean M, Aker Saundra N, Salazar Raymond C, McDonald George B
Clinical Research Division, Fred Hutchinson Cancer Research Center and the University of Washington School of Medicine, Seattle, 98109, USA.
Blood. 2006 Jul 15;108(2):749-55. doi: 10.1182/blood-2006-01-0254. Epub 2006 Mar 14.
Algorithms for grading acute graft-versus-host disease (GVHD) are inaccurate in assessing mortality risk. We developed a method to predict mortality by using data from 386 patients with acute GVHD. From the onset of GVHD to day 100, GVHD manifestations were scored for the skin, liver, and upper and lower gastrointestinal tract, and data were recorded for immunosuppressive treatment, performance, and fever. Logistic regression models predicting nonrelapse mortality (NRM) at day 200 were developed with data from 193 randomly selected patients and then validated in the remaining 193 patients. Clinical parameters were grouped to optimize predictive accuracy measured as the area under a receiver-operator characteristic (ROC) curve. The optimal model included the total serum bilirubin concentration, oral intake, need for treatment with prednisone, and performance score. When the overall burden of GVHD was measured by using average Acute GVHD Activity Index (aGVHDAI) scores for each patient in training and validation data sets, areas under ROC curves were 0.87 and 0.85, respectively. Contour lines were generated to reflect the predicted NRM at day 200 as a function of current aGVHDAI scores. These results demonstrate that clinical manifestations of GVHD severity can be used to accurately predict the risk of NRM in real time.
用于评估急性移植物抗宿主病(GVHD)分级的算法在评估死亡风险方面并不准确。我们开发了一种利用386例急性GVHD患者的数据来预测死亡率的方法。从GVHD发病至第100天,对皮肤、肝脏以及上、下胃肠道的GVHD表现进行评分,并记录免疫抑制治疗、身体状况和发热的数据。利用193例随机选择患者的数据建立预测第200天非复发死亡率(NRM)的逻辑回归模型,然后在其余193例患者中进行验证。对临床参数进行分组,以优化以受试者工作特征(ROC)曲线下面积衡量的预测准确性。最佳模型包括总血清胆红素浓度、口服摄入量、泼尼松治疗需求和身体状况评分。当使用训练和验证数据集中每位患者的平均急性GVHD活动指数(aGVHDAI)评分来衡量GVHD的总体负担时,ROC曲线下面积分别为0.87和0.85。生成等高线以反映第200天预测的NRM作为当前aGVHDAI评分的函数。这些结果表明,GVHD严重程度的临床表现可用于实时准确预测NRM风险。