University of Michigan Blood and Marrow Transplant Program, Ann Arbor, USA.
Blood. 2012 Apr 19;119(16):3854-60. doi: 10.1182/blood-2012-01-403063. Epub 2012 Mar 1.
Acute graft-versus-host disease (GVHD) is the primary limitation of allogeneic hematopoietic cell transplantation, and once it develops, there are no reliable diagnostic tests to predict treatment outcomes. We hypothesized that 6 previously validated diagnostic biomarkers of GVHD (IL-2 receptor-α; tumor necrosis factor receptor-1; hepatocyte growth factor; IL-8; elafin, a skin-specific marker; and regenerating islet-derived 3-α, a gastrointestinal tract-specific marker) could discriminate between therapy responsive and nonresponsive patients and predict survival in patients receiving GVHD therapy. We measured GVHD biomarker concentrations from samples prospectively obtained at the initiation of treatment, day 14, and day 28, on a multicenter, randomized, 4-arm phase 2 clinical trial for newly diagnosed acute GVHD. We found that at each of 3 time points, GVHD onset, 2 weeks into treatment, and 4 weeks into treatment, a 6-protein biomarker panel predicted for the important clinical outcomes of day 28 posttherapy nonresponse and mortality at day 180 from onset. GVHD biomarker panels can be used for early identification of patients at high or low risk for treatment nonresponsiveness or death, and they may provide opportunities for early intervention and improved survival after hematopoietic cell transplantation. The study was registered in clinicaltrials.gov as NCT00224874.
急性移植物抗宿主病(GVHD)是异基因造血细胞移植的主要限制因素,一旦发生,目前尚无可靠的诊断试验来预测治疗结果。我们假设,6 种先前验证的 GVHD 诊断生物标志物(白细胞介素 2 受体-α;肿瘤坏死因子受体-1;肝细胞生长因子;白细胞介素 8;elafin,一种皮肤特异性标志物;和再生胰岛衍生 3-α,一种胃肠道特异性标志物)可以区分治疗有反应和无反应的患者,并预测接受 GVHD 治疗的患者的生存情况。我们在一项新诊断的急性 GVHD 的多中心、随机、4 臂 2 期临床试验中,前瞻性地测量了治疗开始时、第 14 天和第 28 天获得的样本中的 GVHD 生物标志物浓度。我们发现,在 3 个时间点(GVHD 发作、治疗开始后 2 周和 4 周),6 种蛋白质生物标志物组合均能预测治疗后第 28 天无反应和发病后第 180 天死亡的重要临床结局。GVHD 生物标志物组合可用于早期识别治疗无反应或死亡风险高或低的患者,并且可能为造血细胞移植后的早期干预和提高生存率提供机会。该研究在 clinicaltrials.gov 上注册为 NCT00224874。