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芦可替尼治疗急性皮质类固醇难治性移植物抗宿主病:一项范围综述

Ruxolitinib in the Treatment of Acute Corticosteroid-Refractory Graft-Versus-Host Disease: A Scoping Review.

作者信息

Schramm do Nascimento Maria Augusta, Filho Solimar Ribeiro Carlete, Miranda Mariana Daga, Mendes Antonio Eduardo Matoso, de Paula E Silva Carneiro Mendes de Souza Gisele, Borba Helena Hiemisch Lobo

机构信息

Clinics Hospital Complex of the Federal University of Paraná, Curitiba, Brazil.

Department of Pharmacy, Federal University of Paraná, Curitiba, Brazil.

出版信息

Transplant Cell Ther. 2025 Aug;31(8):569.e1-569.e9. doi: 10.1016/j.jtct.2025.04.018. Epub 2025 May 8.

Abstract

BACKGROUND

Graft-versus-Host Disease (GVHD) is a common complication following allogeneic hematopoietic stem cell transplantation (HSCT) and is considered one of the leading causes of post-transplant morbidity and mortality. Acute GVHD (aGVHD) primarily affects the skin, gastrointestinal tract, and liver. Despite advances in immunoprophylaxis, 20% to 80% of patients develop aGVHD, of whom only 60% respond to first-line treatment (e.g., methylprednisolone). Ruxolitinib, a selective inhibitor of Janus Kinase (JAK) 1 and 2, has been proposed as a treatment option following failure of first-line therapy.

OBJECTIVE

The present study aims to map the current evidence regarding the use of ruxolitinib in the treatment of glucocorticoid-refractory aGVHD in patients with hematologic diseases undergoing allogeneic HSCT.

STUDY DESIGN

We performed a scoping review in accordance with the Joanna Briggs Institute guidelines. Systematic searches were performed in the PubMed and Scopus databases in December 2024, with no restrictions on year or language. Two independent reviewers carried out article selection and data extraction.

RESULTS

A total of 1162 studies were screened, with 13 matching the inclusion criteria. The articles were published between 2016 and 2024 and originated from developed countries, with the majority from China (33.8%) and Germany (23.1%), being predominantly retrospective cohort studies (38.5%) and case reports or case series (38.5%). The main adverse effects reported included infections, viral reactivation, and pancytopenia. The overall response rates were 65.0% for combination therapy and 67.4% in comparison with other therapies. All patients who received monotherapy achieved a complete or partial response to treatment, however, the studies involved small sample sizes, limiting the ability to extrapolate these findings.

CONCLUSIONS

Ruxolitinib demonstrates therapeutic potential in this context; however, higher-level primary studies, such as randomized controlled trials, are necessary to achieve more robust conclusions.

摘要

背景

移植物抗宿主病(GVHD)是异基因造血干细胞移植(HSCT)后常见的并发症,被认为是移植后发病和死亡的主要原因之一。急性GVHD(aGVHD)主要影响皮肤、胃肠道和肝脏。尽管免疫预防取得了进展,但20%至80%的患者会发生aGVHD,其中只有60%对一线治疗(如甲泼尼龙)有反应。芦可替尼是一种Janus激酶(JAK)1和2的选择性抑制剂,已被提议作为一线治疗失败后的治疗选择。

目的

本研究旨在梳理目前关于芦可替尼用于治疗接受异基因HSCT的血液病患者糖皮质激素难治性aGVHD的证据。

研究设计

我们按照乔安娜·布里格斯研究所的指南进行了一项范围综述。2024年12月在PubMed和Scopus数据库中进行了系统检索,对年份和语言没有限制。两名独立评审员进行文章筛选和数据提取。

结果

共筛选了1162项研究,13项符合纳入标准。这些文章发表于2016年至2024年之间,来自发达国家,其中大部分来自中国(33.8%)和德国(23.1%),主要是回顾性队列研究(38.5%)和病例报告或病例系列(38.5%)。报告的主要不良反应包括感染、病毒再激活和全血细胞减少。联合治疗的总体缓解率为65.0%,与其他疗法相比为67.4%。所有接受单药治疗的患者均对治疗有完全或部分反应,然而,这些研究样本量较小,限制了外推这些结果的能力。

结论

在这种情况下,芦可替尼显示出治疗潜力;然而,需要更高水平的原始研究,如随机对照试验,以得出更可靠的结论。

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