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Acute graft-versus-host disease biomarkers measured during therapy can predict treatment outcomes: a Blood and Marrow Transplant Clinical Trials Network study

机译:治疗期间测量的急性移植物抗宿主疾病生物标志物可以预测治疗结果:一项血液和骨髓移植临床试验网络研究

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摘要

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 .
机译:急性移植物抗宿主病(GVHD)是同种异体造血细胞移植的主要局限性,一旦发展,就没有可靠的诊断测试可预测治疗结果。我们假设有6个先前已验证的GVHD诊断生物标记物(IL-2受体-α;肿瘤坏死因子受体-1;肝细胞生长因子; IL-8;皮肤特异性标记物elafin;以及再生的胰岛来源的3-α,胃肠道特异性标志物)可以区分治疗反应敏感和无反应患者,并预测接受GVHD治疗的患者的存活率。我们在多中心,随机,4组第2期临床试验中,从开始治疗的第14天和第28天前瞻性获得的样本中测量了GVHD生物标志物浓度,用于新诊断的急性GVHD。我们发现,在GVHD发作,治疗2周和治疗4周这3个时间点的每一个时间点,一个6蛋白生物标志物组都预测了治疗后第28天无反应的重要临床结果以及发病后第180天的死亡率。 GVHD生物标记物面板可用于早期识别治疗无反应性或死亡的高风险或低风险的患者,它们可能为早期干预和改善造血细胞移植后的存活率提供机会。该研究已在Clinicaltrials.gov中注册为。

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