Evaluation of Combination Therapy With Etanercept and Systemic Corticosteroids for Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: A Multicenter Observational Study

中毒性表皮坏死松解 医学 依那西普 联合疗法 皮质类固醇 不利影响 皮肤病科 内科学 外科 肿瘤坏死因子α
作者
Jing Zhang,Chun‐Wei Lu,Chun‐Bing Chen,Chuang‐Wei Wang,Wei‐Ti Chen,Bo Cheng,Chao Ji,Wen‐Hung Chung
出处
期刊:The Journal of Allergy and Clinical Immunology: In Practice [Elsevier BV]
卷期号:10 (5): 1295-1304.e6 被引量:31
标识
DOI:10.1016/j.jaip.2022.01.038
摘要

Background

Stevens-Johnson syndrome–toxic epidermal necrolysis (SJS-TEN) are fatal severe cutaneous adverse reactions, without consensus on the medical treatment. The use of systemic corticosteroids or intravenous immunoglobulin (IVIG) remains debatable. Tumor necrosis factor–alpha inhibitors are potentially effective.

Objective

To evaluate the effectiveness and safety of combination therapy using etanercept combined with corticosteroids or IVIG combined with corticosteroids versus corticosteroid monotherapy for patients with SJS-TEN.

Methods

We retrospectively enrolled SJS-TEN patients from Taiwan and the Chinese mainland, during 2014 to 2019. Patients enrolled were treated with corticosteroid monotherapy, or combinations with IVIG or etanercept. We analyzed the clinical characteristics, skin healing time, mortality, and adverse events among these treatment groups.

Results

Among the 242 patients (187 with SJS or SJS-TEN overlapping and 55 with TEN), patients who received combination therapy with etanercept and corticosteroids had lower actual mortality than those with corticosteroid monotherapy and those with IVIG combined with corticosteroids, respectively (0% vs 6.63% and 4.76%). There was a tendency of reducing standardized (observed/predicted) mortality rate (SMR) based on the Score of Toxic Epidermal Necrolysis in etanercept combined with corticosteroids compared with corticosteroid monotherapy and IVIG combined with corticosteroids therapy (SMR [95% CI] 0 [1.80–3.59], 0.71 [0.83–2.64], 0.30 [0.68–6.22]; P = .006). Etanercept combined with corticosteroids showed a reduced skin healing time (12.0 [8.5–14.0], median days [interquartile range]), compared with corticosteroid monotherapy (13.0 [10.0–18.0]) and IVIG combined with corticosteroids therapy (13.5 [10.0–19.5]); P = .004 and P = .012, respectively). Etanercept combined with corticosteroids also showed a lower incidence of adverse event with gastrointestinal hemorrhage than corticosteroid monotherapy, especially in patients with TEN (P = .001).

Conclusions

The tumor necrosis factor–alpha inhibitors and corticosteroids combination therapy was effective and safer than corticosteroid monotherapy for SJS-TEN, and may be considered as an alternative therapy for SJS-TEN patients who responded poorly to conventional corticosteroid therapy.
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