Systemic steroid treatment of grade I acute GVHD increases steroid-refractory GVHD and NRM.

Blood immunology & cellular therapy. Pub Date : 2026-06-01 Epub Date: 2026-04-29 DOI:10.1016/j.bict.2026.100044
Yu Akahoshi, Nikolaos Katsivelos, Ioannis E Louloudis, Daniela Weber, Francis Ayuk, William J Hogan, Yi-Bin Chen, Aaron M Etra, Paibel Aguayo-Hiraldo, Chantiya Chanswangphuwana, Hannah K Choe, Elizabeth O Hexner, Carrie L Kitko, Monzr M Al Malki, Pietro Merli, Timothy S Olson, Muna Qayed, Ingrid Vasova, Matthias Wölfl, Janna Baez, Gilbert Eng, Sigrun Gleich, George Morales, Nikolaos Spyrou, Rachel Young, Marcio Diniz, Ryotaro Nakamura, John E Levine, James L M Ferrara
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Abstract

The use of systemic corticosteroids is recommended only for grades II to IV acute graft-versus-host disease (GVHD), but many patients are often treated at the onset of grade I in real-world practice. We retrospectively analyzed outcomes of 1143 patients with grade I GVHD from 24 Mount Sinai Acute GVHD International Consortium (MAGIC) transplant centers. Approximately half received "up-front" systemic steroids, whereas the remainder received topical steroids alone; GVHD progressed to grade II to IV in only one-third of these patients. Up-front steroids decreased the risk for grade II to IV GVHD but not grade III to IV acute GVHD or the need for a second line of treatment. Systemic steroids were equally effective at treating grade I or II GVHD; however, up-front therapy exposed 3 times more patients to systemic steroids, with a corresponding threefold increase in GVHD that required additional therapy and a threefold rise in infection-related deaths. In multivariable analyses, up-front steroids were significantly associated with higher nonrelapse mortality (NRM; P = .026). MAGIC biomarkers identified most patients with grade I GVHD as low risk and unlikely to progress to severe GVHD regardless of treatment. Nevertheless, low-risk patients who received up-front steroids experienced a threefold increase in infectious deaths compared with those treated topically. This study supports the consensus recommendation of topical therapy for patients with low-risk grade I GVHD, a strategy that can be supported by biomarkers to avoid unnecessary steroid exposure and increased NRM.

I级急性GVHD的全身类固醇治疗增加类固醇难治性GVHD和NRM。
全身性皮质类固醇仅推荐用于II至IV级急性移植物抗宿主病(GVHD),但在现实世界的实践中,许多患者通常在I级发病时接受治疗。我们回顾性分析了来自24个西奈山急性GVHD国际联盟(MAGIC)移植中心的1143例I级GVHD患者的结局。大约一半的患者接受了“预先”全身性类固醇治疗,而其余患者仅接受局部类固醇治疗;这些患者中只有三分之一的GVHD进展到II至IV级。预先类固醇降低了II至IV级GVHD的风险,但没有降低III至IV级急性GVHD或需要二线治疗的风险。全身性类固醇治疗I级或II级GVHD同样有效;然而,预先治疗使接受全身性类固醇治疗的患者增加了3倍,GVHD相应增加了3倍,需要额外治疗,感染相关死亡增加了3倍。在多变量分析中,预先使用类固醇与较高的非复发死亡率显著相关(NRM; P = 0.026)。MAGIC生物标志物将大多数I级GVHD患者识别为低风险,无论如何治疗都不太可能进展为严重GVHD。然而,接受预先类固醇治疗的低风险患者的感染性死亡比局部治疗的患者增加了三倍。本研究支持对低风险I级GVHD患者进行局部治疗的共识建议,该策略可以得到生物标志物的支持,以避免不必要的类固醇暴露和增加NRM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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