Department of Laboratory Medicine, the First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Department of Internal Medicine, Mercer University School of Medicine, Macon, GA, USA.
Orphanet J Rare Dis. 2020 Mar 12;15(1):71. doi: 10.1186/s13023-020-1336-6.
Hemophagocytic Lymphohistiocytosis (HLH) is a rare clinical syndrome with high mortality rate. The diagnosis of HLH draws on a constellation of clinical and laboratory abnormalities including extremely high serum ferritin levels. However, no biomarker has been firmly established as a clinically useful prognostic tool in HLH patients. We aimed to perform a retrospective analysis of two independent cohorts to explore the prognostic value of discharge serum ferritin for newly diagnosed adult HLH patients who recently started treatment. The prognostic value of serum ferritin levels at discharge (will be called as post-treatment ferritin level) was initially evaluated in a "test cohort" of 161 previously untreated consecutive adult HLH patients. It was then validated in a second cohort of 68 consecutive previously untreated patients (validation cohort).
Multivariate analysis revealed that significantly high post-treatment serum ferritin levels (>1050 μg/L) were associated with a higher risk of death and poor overall survival in the test cohort (hazard ratio (HR): 3.176, 95% confidence interval (CI) 1.468-6.869, P = 0.003), and the validation cohort (HR: 13.412, 95%CI 1.716-104.816, P = 0.013). At 6-month follow-up period in the test cohort, patients with a > 81% decrease in the serum ferritin level had a significantly higher probability of survival when compared with the patients with ≥14% increase in the serum ferritin level (94% vs. 31%, P < 0.001). Similar findings were observed on the analysis of the decrease in the serum ferritin level in the validation cohort.
These results suggest that the serum ferritin level can be used as an independent prognostic marker in the adult HLH patients.
噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见的临床综合征,死亡率高。HLH 的诊断依据包括极高的血清铁蛋白水平在内的一系列临床和实验室异常。然而,在 HLH 患者中,没有一种生物标志物被确定为具有临床应用价值的预后工具。我们旨在对两个独立队列进行回顾性分析,以探讨新诊断的成年 HLH 患者在开始治疗后出院时的血清铁蛋白对预后的预测价值。在一个未经治疗的 161 例成年 HLH 患者的“测试队列”中,首先评估了出院时血清铁蛋白水平(称为治疗后铁蛋白水平)的预后价值。然后在第二个未经治疗的 68 例连续患者队列(验证队列)中进行验证。
多变量分析显示,治疗后血清铁蛋白水平显著升高(>1050μg/L)与测试队列(死亡风险比(HR):3.176,95%置信区间(CI)1.468-6.869,P=0.003)和验证队列(HR:13.412,95%CI 1.716-104.816,P=0.013)的死亡风险和总体生存不良相关。在测试队列的 6 个月随访期间,与血清铁蛋白水平升高≥14%的患者相比,血清铁蛋白水平下降>81%的患者存活的可能性显著更高(94%比 31%,P<0.001)。在验证队列中,也观察到了血清铁蛋白水平下降的类似分析结果。
这些结果表明,血清铁蛋白水平可作为成年 HLH 患者的独立预后标志物。