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阿巴西普作为慢性移植物抗宿主病的挽救性治疗:一项回顾性分析。

Abatacept as salvage therapy in chronic graft-versus-host disease-a retrospective analysis.

机构信息

Department of Internal Medicine III, Hematology and Oncology, University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, 93053, Regensburg, Germany.

Department of Hematology, Oncology and Immunology, University Hospital Giessen and Marburg, Marburg, Germany.

出版信息

Ann Hematol. 2021 Mar;100(3):779-787. doi: 10.1007/s00277-021-04434-x. Epub 2021 Jan 30.

DOI:10.1007/s00277-021-04434-x
PMID:33515310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7914235/
Abstract

The immunomodulatory fusion protein abatacept has recently been investigated for the treatment of steroid-refractory chronic graft-versus-host disease (cGvHD) in a phase 1 clinical trial. We analyzed the safety and efficacy of abatacept for cGvHD therapy in a retrospective study with 15 patients who underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT) and received abatacept for cGvHD with a median age of 49 years. Grading was performed as part of the clinical routine according to the National Institute of Health's (NIH) consensus criteria at initiation of abatacept and 1, 3, 6, 9 and 12 months thereafter. The median time of follow-up was 191 days (range 55-393 days). Best overall response rate (ORR) was 40%. In particular, patients with bronchiolitis obliterans syndrome showed significant clinical improvement and durable responses following abatacept treatment with a response rate of 89% based on improvement in lung severity score (n = 6) or stabilized lung function (n = 4) or both (n = 3). Infectious complications CTCAE °III or higher were observed in 3/15 patients. None of the patients relapsed from the underlying malignancy. Thus, abatacept appears to be a promising treatment option for cGvHD, in particular for patients with lung involvement. However, further evaluation within a phase 2 clinical trial is required.

摘要

免疫调节融合蛋白阿巴西普最近在一项 1 期临床试验中被研究用于治疗类固醇难治性慢性移植物抗宿主病(cGvHD)。我们对 15 例接受异基因造血干细胞移植(allo-HSCT)并接受阿巴西普治疗 cGvHD 的患者进行了回顾性研究,分析了阿巴西普治疗 cGvHD 的安全性和疗效。这些患者的中位年龄为 49 岁。根据美国国立卫生研究院(NIH)共识标准,在开始使用阿巴西普以及之后的 1、3、6、9 和 12 个月进行分级,该分级是临床常规的一部分。中位随访时间为 191 天(范围 55-393 天)。总体最佳反应率(ORR)为 40%。特别是,有 6 例患者的细支气管炎闭塞综合征(bronchiolitis obliterans syndrome)根据肺严重程度评分的改善(n = 6)或稳定的肺功能(n = 4)或两者均有改善(n = 3)显示出显著的临床改善和持久反应,反应率为 89%。在 15 例患者中观察到 3 例(20%)出现 CTCAE °III 级或更高的感染并发症。没有患者从基础恶性肿瘤复发。因此,阿巴西普似乎是 cGvHD 的一种有前途的治疗选择,特别是对于有肺部受累的患者。然而,需要在 2 期临床试验中进一步评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5629/7914235/b7f6c514040d/277_2021_4434_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5629/7914235/5d3ab79055d9/277_2021_4434_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5629/7914235/b7f6c514040d/277_2021_4434_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5629/7914235/5d3ab79055d9/277_2021_4434_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5629/7914235/b7f6c514040d/277_2021_4434_Fig2_HTML.jpg

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