Macrophage Activation Syndrome in Adults: Characteristics, Outcomes, and Therapeutic Effectiveness of Etoposide-based Regimen
Overview
Affiliations
Objectives: To describe the clinical characteristics and outcomes of adult macrophage activation syndrome (MAS) patients and to provide experience for the treatment.
Methods: Adult 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.
Results: A 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-γ (P = 0.013), IP-10 (P = 0.001), IL-10 (P = 0.041), IL-1RA (P < 0.001), and TNF-α (P = 0.020) levels of patients were significantly decreased in the remission phase than in the active phase. Levels of SDF-1α (P = 0.018) and IL-7 (P = 0.022) were higher in refractory patients, while the GRO-α 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 × 10/l [P = 0.017, HR = 3.678, 95% CI, (1.267, 10.672)] were negative prognostic factors.
Conclusion: MAS typically occurs within 2 months after the onset of autoimmune disease in adults. SDF-1α, IL-7, and GRO-α could be used to predict refractory MAS. The etoposide-based regimen is effective and tolerable for adult MAS.
Gao T, Suolitiken D, Yang C, Wu C, He L, Wang Y Clin Exp Med. 2025; 25(1):58.
PMID: 39955467 PMC: 11829903. DOI: 10.1007/s10238-025-01570-w.
Gao S, Luo X, Kosari M, Li W, Yang L, Tu W World J Radiol. 2024; 16(10):579-585.
PMID: 39494131 PMC: 11525825. DOI: 10.4329/wjr.v16.i10.579.
Yin D, Wang J, Wang Z Ann Hematol. 2024; 103(9):3463-3472.
PMID: 38772957 DOI: 10.1007/s00277-024-05796-8.
Lin W, Xie X, Luo Z, Chen X, Cao H, Fang X Arthritis Res Ther. 2024; 26(1):92.
PMID: 38725078 PMC: 11080238. DOI: 10.1186/s13075-024-03330-9.
Advances in attractive therapeutic approach for macrophage activation syndrome in COVID-19.
Chen S, Zhang C, Chen D, Dong L, Chang T, Tang Z Front Immunol. 2023; 14:1200289.
PMID: 37483597 PMC: 10358730. DOI: 10.3389/fimmu.2023.1200289.