Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, MI.
Blood. 2018 Jun 21;131(25):2846-2855. doi: 10.1182/blood-2018-01-822957. Epub 2018 Mar 15.
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.
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。