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芦可替尼联合皮质类固醇作为新诊断高危急性移植物抗宿主病一线治疗的研究方案:一项多中心、随机、二期对照临床试验。

Ruxolitinib-corticosteroid as first-line therapy for newly diagnosed high-risk acute graft versus host disease: study protocol for a multicenter, randomized, phase II controlled trial.

机构信息

Department of Hematology, The Fifth Medical Center of Chinese PLA General Hospital, No. 28 Fuxing Road, Haidian District, Beijing, 100853, China.

Medical School of Chinese PLA, Beijing, 100853, China.

出版信息

Trials. 2022 Jun 6;23(1):470. doi: 10.1186/s13063-022-06426-2.

Abstract

BACKGROUND

The response rate of the first-line therapy with corticosteroid for acute graft versus host disease (aGVHD) is about 50%, and steroid-refractory disease is associated with high mortality. The improved response rate to the first-line therapy of newly diagnosed aGVHD patients would result in therapeutic benefits. Ruxolitinib, a selective Janus kinase (JAK) 1/2 inhibitor, has been approved for the treatment of steroid-refractory acute GVHD. The addition of ruxolitinib to the first-line therapy may improve the efficacy of corticosteroids.

METHODS

This investigator-initiated, open-label, multicenter, prospective randomized, and controlled two-arm phase II study compares the efficacy and safety of ruxolitinib combined with 1 mg/kg methylprednisolone versus 2 mg/kg methylprednisolone alone in newly diagnosed aGVHD patients. Patients with intermediate or high-risk aGVHD, as defined by the Minnesota aGVHD high-risk score and biomarker algorithm, are eligible for this study. A total of 198 patients will be randomized at a 1:1 ratio and assigned a GVHD risk (intermediate versus high risk) and disease status before transplantation (complete remission versus no complete remission). The primary endpoint is the overall response rate on day 28, which is defined as an improvement of at least one stage in the severity of aGVHD in one organ without deterioration in any other organ or disappearance of any GVHD signs from all organs without requiring new systemic immunosuppressive treatment. The secondary objectives consist of response time, response duration, overall survival, disease-free survival, non-relapse mortality, failure-free survival, and changes in serum levels of proinflammatory cytokines and GVHD-related biomarkers.

DISCUSSION

This open-label, multicenter, two-arm randomized trial will evaluate whether the addition of ruxolitinib combined with corticosteroid is superior to corticosteroid alone in newly diagnosed high-risk aGVHD.

TRIAL REGISTRATION

ClinicalTrials.gov NCT04061876 (version number: 2019.5.18). Registered on July 16, 2019.

摘要

背景

一线治疗急性移植物抗宿主病(aGVHD)的皮质类固醇反应率约为 50%,而类固醇难治性疾病与高死亡率相关。提高新诊断的 aGVHD 患者对一线治疗的反应率将带来治疗益处。鲁索替尼(ruxolitinib),一种选择性 Janus 激酶(JAK)1/2 抑制剂,已被批准用于治疗类固醇难治性急性 GVHD。在一线治疗中加入鲁索替尼可能会提高皮质类固醇的疗效。

方法

这项由研究者发起的、开放性标签、多中心、前瞻性、随机对照、双臂 2 期研究比较了鲁索替尼联合 1mg/kg 甲泼尼龙与单独使用 2mg/kg 甲泼尼龙在新诊断的 aGVHD 患者中的疗效和安全性。符合明尼苏达州 GVHD 高危评分和生物标志物算法定义的中高危 aGVHD 患者有资格参加这项研究。共有 198 名患者将按照 1:1 的比例随机分组,并根据 GVHD 风险(中危与高危)和移植前疾病状态(完全缓解与未完全缓解)进行分组。主要终点是第 28 天的总体缓解率,定义为一个器官的 aGVHD 严重程度至少提高一个级别,而其他任何器官没有恶化,或所有器官的任何 GVHD 迹象消失,且无需新的全身免疫抑制治疗。次要目标包括反应时间、反应持续时间、总生存率、无病生存率、非复发死亡率、无失败生存率以及促炎细胞因子和 GVHD 相关生物标志物的血清水平变化。

讨论

这项开放性标签、多中心、双臂随机试验将评估鲁索替尼联合皮质类固醇是否优于新诊断的高危 aGVHD 患者单独使用皮质类固醇。

试验注册

ClinicalTrials.gov NCT04061876(版本号:2019.5.18)。于 2019 年 7 月 16 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9369/9169300/77bfce25c5f9/13063_2022_6426_Fig1_HTML.jpg

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