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MAGIC 标志物可预测激素耐药性急性移植物抗宿主病的长期结局。

MAGIC biomarkers predict long-term outcomes for steroid-resistant acute GVHD.

机构信息

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.

Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, MI.

出版信息

Blood. 2018 Jun 21;131(25):2846-2855. doi: 10.1182/blood-2018-01-822957. Epub 2018 Mar 15.

Abstract

Acute graft-versus-host disease (GVHD) is treated with systemic corticosteroid immunosuppression. Clinical response after 1 week of therapy often guides further treatment decisions, but long-term outcomes vary widely among centers, and more accurate predictive tests are urgently needed. We analyzed clinical data and blood samples taken 1 week after systemic treatment of GVHD from 507 patients from 17 centers of the Mount Sinai Acute GVHD International Consortium (MAGIC), dividing them into a test cohort (n = 236) and 2 validation cohorts separated in time (n = 142 and n = 129). Initial response to systemic steroids correlated with response at 4 weeks, 1-year nonrelapse mortality (NRM), and overall survival (OS). A previously validated algorithm of 2 MAGIC biomarkers (ST2 and REG3α) consistently separated steroid-resistant patients into 2 groups with dramatically different NRM and OS ( < .001 for all 3 cohorts). High biomarker probability, resistance to steroids, and GVHD severity (Minnesota risk) were all significant predictors of NRM in multivariate analysis. A direct comparison of receiver operating characteristic curves showed that the area under the curve for biomarker probability (0.82) was significantly greater than that for steroid response (0.68, = .004) and for Minnesota risk (0.72, = .005). In conclusion, MAGIC biomarker probabilities generated after 1 week of systemic treatment of GVHD predict long-term outcomes in steroid-resistant GVHD better than clinical criteria and should prove useful in developing better treatment strategies.

摘要

急性移植物抗宿主病(GVHD)采用全身性皮质类固醇免疫抑制治疗。治疗 1 周后的临床反应通常指导进一步的治疗决策,但各中心的长期结果差异很大,迫切需要更准确的预测性测试。我们分析了来自 Mount Sinai 急性 GVHD 国际联合会(MAGIC)的 17 个中心的 507 名患者的临床数据和治疗 1 周后采集的血液样本,将他们分为测试队列(n=236)和 2 个时间分离的验证队列(n=142 和 n=129)。全身性类固醇治疗后 1 周的初始反应与 4 周、1 年非复发死亡率(NRM)和总生存率(OS)相关。之前验证过的 2 个 MAGIC 生物标志物(ST2 和 REG3α)算法一致地将类固醇耐药患者分为 2 组,这两组的 NRM 和 OS 差异显著(所有 3 个队列均<.001)。生物标志物概率高、对类固醇耐药和 GVHD 严重程度(明尼苏达风险)均是多变量分析中 NRM 的显著预测因素。对受试者工作特征曲线的直接比较显示,生物标志物概率的曲线下面积(AUC)(0.82)明显大于类固醇反应(0.68,P=.004)和明尼苏达风险(0.72,P=.005)。总之,GVHD 全身性治疗 1 周后产生的 MAGIC 生物标志物概率比临床标准更好地预测了类固醇耐药性 GVHD 的长期结局,应该有助于制定更好的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45f5/6014357/d1e860efd019/blood822957absf1.jpg

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