4.8 Article

Macrophage activation syndrome in adults: Characteristics, outcomes, and therapeutic effectiveness of etoposide-based regimen

期刊

FRONTIERS IN IMMUNOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.955523

关键词

hemophagocytic lymphohistiocytosis (HLH); macrophage activation syndrome (MAS); autoimmune disease (AID); cytokine; etoposide; adult

资金

  1. National Natural Science Foundation of China
  2. [82170122]
  3. [81871633]

向作者/读者索取更多资源

This study described the clinical characteristics and outcomes of adult macrophage activation syndrome (MAS) patients. The results showed that MAS typically occurs within 2 months after the onset of autoimmune disease in adults. The etoposide-based regimen is effective and tolerable for adult MAS.
ObjectivesTo describe the clinical characteristics and outcomes of adult macrophage activation syndrome (MAS) patients and to provide experience for the treatment. MethodsAdult patients with MAS admitted to Beijing Friendship Hospital from December 2014 to September 2021 were enrolled in this study. Clinical data of patients were collected and analyzed. ResultsA total of 118 adult MAS patients entered this study. MAS was the first manifestation in 43 (36.4%) patients, while 75 (63.6%) developed MAS after the diagnosis of autoimmune disease (AID) with a median diagnostic interval of 2 (0.5-359) months. Eighty-two patients were initially treated with glucocorticoid-based regimen; the overall response (OR) rate at the 2-week posttreatment was 37.8%. Forty-five patients switched to etoposide-based regimen, and the OR rate was 84.4%. Thirty-six patients were initially treated with etoposide-based regimen, and the OR rate at the 2-week posttreatment was 80.6%. Serum IL-18 (P = 0.021), IFN-gamma (P = 0.013), IP-10 (P = 0.001), IL-10 (P = 0.041), IL-1RA (P < 0.001), and TNF-alpha (P = 0.020) levels of patients were significantly decreased in the remission phase than in the active phase. Levels of SDF-1 alpha (P = 0.018) and IL-7 (P = 0.022) were higher in refractory patients, while the GRO-alpha level had a strong tendency toward statistical significance (P = 0.050). The probability of overall survival (OS) at 3, 6, and 36 months after HLH diagnosis were 89.8%, 89.0%, and 87.9%, retrospectively. The active MAS status at the 2-week post initial treatment [P = 0.009, HR = 15.281, 95% CI, (0.1.972, 118.430)] and baseline neutrophil count (Neu) <1.5 x 10(9)/l [P = 0.017, HR = 3.678, 95% CI, (1.267, 10.672)] were negative prognostic factors. ConclusionMAS typically occurs within 2 months after the onset of autoimmune disease in adults. SDF-1 alpha, IL-7, and GRO-alpha could be used to predict refractory MAS. The etoposide-based regimen is effective and tolerable for adult MAS.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据