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移植物抗宿主病治疗:生存预测因素。

Graft-versus-host disease treatment: predictors of survival.

机构信息

Departments of Pediatrics and Internal Medicine, University of Michigan, 1500 E. Medical Center Drive, Ann Arbor, MI 48109-5941, USA.

出版信息

Biol Blood Marrow Transplant. 2010 Dec;16(12):1693-9. doi: 10.1016/j.bbmt.2010.05.019. Epub 2010 Jun 9.

DOI:10.1016/j.bbmt.2010.05.019
PMID:20541024
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2955996/
Abstract

Acute graft-versus-host disease (aGVHD) following allogeneic hematopoietic cell transplant (HCT) is the major reason for nonrelapse mortality (NRM), and thus is a major determinant of long-term survival. Clinical trials of new aGVHD treatments are needed to identify approaches that will ultimately improve upon HCT survival. At present, it is not clear how quickly response to GVHD treatment needs to be established to reliably categorize patients at high risk for death or to promptly identify those who might benefit from alternate treatment. Therefore, we analyzed time to response from onset of aGVHD treatment in 180 patients who were enrolled on a national, randomized, phase II aGVHD treatment clinical trial whose initial treatment of GVHD consisted of high-dose steroids plus a second immunosuppressive agent. The aim of this analysis was to determine whether time to aGVHD treatment response predicts patient outcomes, especially survival. We used response at 14, 28, and 56 days from initiation of aGVHD treatment to categorize patients for NRM and survival. Multivariate analyses and specificity/sensitivity analyses identified that day 28 response (complete or partial response) best categorized patients by NRM and survival at 9 months from start of aGVHD treatment. If verified as a reliable predictor of late outcomes following other aGVHD treatment approaches, day 28 response should serve as a standard early endpoint for future trials of aGVHD therapy.

摘要

异基因造血细胞移植(HCT)后发生的急性移植物抗宿主病(aGVHD)是导致非复发死亡率(NRM)的主要原因,也是长期生存的主要决定因素。需要进行新的 aGVHD 治疗临床试验,以确定能够最终提高 HCT 生存率的方法。目前,尚不清楚需要多快建立对 GVHD 治疗的反应,以便可靠地将高死亡风险的患者分类,或者及时确定那些可能受益于替代治疗的患者。因此,我们分析了在 180 名患者中的反应时间,这些患者参与了一项全国性、随机、II 期 aGVHD 治疗临床试验,该试验的初始 GVHD 治疗包括大剂量类固醇加第二种免疫抑制剂。本分析的目的是确定 aGVHD 治疗反应的时间是否可以预测患者的结局,尤其是生存情况。我们使用从开始治疗 aGVHD 后 14、28 和 56 天的反应来对患者进行 NRM 和生存情况分类。多变量分析和特异性/敏感性分析表明,第 28 天的反应(完全或部分反应)能够根据从开始治疗 aGVHD 后 9 个月的 NRM 和生存情况对患者进行最佳分类。如果被证实为其他 aGVHD 治疗方法的晚期结局的可靠预测因素,那么第 28 天的反应应作为未来 aGVHD 治疗试验的标准早期终点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f6b/2955996/b1a4f661d651/nihms214451f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f6b/2955996/b1a4f661d651/nihms214451f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f6b/2955996/b1a4f661d651/nihms214451f1.jpg

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Elafin is a biomarker of graft-versus-host disease of the skin.Elafin 是皮肤移植物抗宿主病的生物标志物。
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Increase in FOXP3+ regulatory T cells in GVHD skin biopsies is associated with lower disease severity and treatment response.移植物抗宿主病皮肤活检中FOXP3 +调节性T细胞的增加与较低的疾病严重程度和治疗反应相关。
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Graft-versus-host disease.移植物抗宿主病
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