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本文引用的文献

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Ruxolitinib for the treatment of patients with steroid-refractory GVHD: an introduction to the REACH  trials.芦可替尼用于治疗类固醇难治性移植物抗宿主病患者:REACH试验介绍
Immunotherapy. 2018 Apr;10(5):391-402. doi: 10.2217/imt-2017-0156. Epub 2018 Jan 10.
2
Compassionate use of ruxolitinib in acute and chronic graft versus host disease refractory both to corticosteroids and extracorporeal photopheresis.芦可替尼在对皮质类固醇和体外光化学疗法均难治的急慢性移植物抗宿主病中的同情用药。
Exp Hematol Oncol. 2017 Dec 2;6:32. doi: 10.1186/s40164-017-0092-3. eCollection 2017.
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No Relapse of Calcineurin Inhibitor-Associated Thrombotic Microangiopathy after Discontinuation of Eculizumab.
Acta Haematol. 2017;138(4):194-197. doi: 10.1159/000481724. Epub 2017 Nov 15.
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Effect of Rituximab on Pulmonary Function in Bronchiolitis Obliterans Syndrome due to Graft-Versus-Host-Disease.利妥昔单抗对移植物抗宿主病致闭塞性细支气管炎综合征患者肺功能的影响。
Lung. 2017 Dec;195(6):781-788. doi: 10.1007/s00408-017-0051-0. Epub 2017 Sep 11.
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Ruxolitinib as a promising treatment for corticosteroid-refractory graft-versus-host disease.芦可替尼作为治疗皮质类固醇难治性移植物抗宿主病的一种有前景的疗法。
Br J Haematol. 2018 Jun;181(5):687-689. doi: 10.1111/bjh.14679. Epub 2017 Apr 25.
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Ruxolitinib as Salvage Therapy in Steroid-Refractory Acute Graft-versus-Host Disease in Pediatric Hematopoietic Stem Cell Transplant Patients.芦可替尼作为儿童造血干细胞移植患者类固醇难治性急性移植物抗宿主病的挽救疗法
Biol Blood Marrow Transplant. 2017 Jul;23(7):1122-1127. doi: 10.1016/j.bbmt.2017.03.029. Epub 2017 Mar 23.
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Ruxolitinib treatment for GvHD in patients with myelofibrosis.芦可替尼治疗骨髓纤维化患者的移植物抗宿主病
Bone Marrow Transplant. 2016 Dec;51(12):1584-1587. doi: 10.1038/bmt.2016.256. Epub 2016 Oct 10.
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How I treat acute graft-versus-host disease of the gastrointestinal tract and the liver.我如何治疗胃肠道和肝脏的急性移植物抗宿主病。
Blood. 2016 Mar 24;127(12):1544-50. doi: 10.1182/blood-2015-10-612747. Epub 2016 Jan 4.
9
Acute Graft-versus-Host Disease: Novel Biological Insights.急性移植物抗宿主病:新的生物学见解
Biol Blood Marrow Transplant. 2016 Jan;22(1):11-6. doi: 10.1016/j.bbmt.2015.10.001. Epub 2015 Oct 26.
10
Ruxolitinib in corticosteroid-refractory graft-versus-host disease after allogeneic stem cell transplantation: a multicenter survey.芦可替尼用于异基因干细胞移植后对皮质类固醇难治的移植物抗宿主病:一项多中心调查
Leukemia. 2015 Oct;29(10):2062-8. doi: 10.1038/leu.2015.212. Epub 2015 Jul 31.

芦可替尼治疗移植物抗宿主病。

Ruxolitinib for Therapy of Graft-versus-Host Disease.

机构信息

University Medicine Greifswald, Internal Medicine C, Hematology and Oncology, Stem Cell Transplantation and Palliative Care, Ferdinand-Sauerbruch-Strasse, 17475 Greifswald, Germany.

出版信息

Biomed Res Int. 2019 Mar 6;2019:8163780. doi: 10.1155/2019/8163780. eCollection 2019.

DOI:10.1155/2019/8163780
PMID:30956985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6431395/
Abstract

OBJECTIVE

Steroid-resistant graft-versus-host disease (GvHD) is a major challenge after allogeneic stem cell transplantation and associated with significant morbidity and mortality. There is no therapeutic standard defined beyond calcineurin inhibitors (CNI) and steroids. Furthermore, some patients may have contraindications against CNI or high-dose steroids. Efficacy of ruxolitinib against GvHD has been described recently.

METHODS

Ruxolitinib was used for treatment of acute or chronic GvHD in eight patients. The patients either needed intensification of therapy or had contraindications against use of CNI or high-dose steroids.

RESULTS

Supplementation of therapy in acute GvHD with severe diarrhea with ruxolitinib was unsuccessful. All these patients died from acute GvHD. Introduction of ruxolitinib into therapy and relapse prophylaxis in other patients was successful in 4/4 cases (CR=3, PR=1). Indications for ruxolitinib were contraindications against CNI due to aHUS in two cases and the need for steroid sparing in two other cases. None of these patients suffered from diarrhea at the initiation of ruxolitinib.

CONCLUSION

Ruxolitinib was effective for therapy of acute and chronic GvHD in higher lines in patients without severe diarrhea. Ruxolitinib could replace successfully CNI and high-dose steroids. Further investigations are necessary to define the position of ruxolitinib in GvHD-therapy.

摘要

目的

异体干细胞移植后发生的激素耐药性移植物抗宿主病(GVHD)是一个重大挑战,与较高的发病率和死亡率相关。除钙调磷酸酶抑制剂(CNI)和激素外,目前尚无明确的治疗标准。此外,一些患者可能存在 CNI 或大剂量激素应用禁忌。近期有研究描述了鲁索利替尼治疗 GVHD 的疗效。

方法

我们采用鲁索利替尼治疗 8 例急性或慢性 GVHD 患者。这些患者需要强化治疗或存在 CNI 或大剂量激素应用禁忌。

结果

在伴有严重腹泻的急性 GVHD 患者中,补充应用鲁索利替尼的治疗方案未能成功。所有这些患者均因急性 GVHD 死亡。在其他患者中,鲁索利替尼被用于引入治疗和预防疾病复发,4 例患者中(完全缓解 3 例,部分缓解 1 例)均取得成功。应用鲁索利替尼的适应证为 2 例患者因溶血尿毒综合征存在 CNI 应用禁忌,2 例患者需要激素减停。这些患者在开始应用鲁索利替尼时均无腹泻。

结论

在无严重腹泻的更高线治疗中,鲁索利替尼对急性和慢性 GVHD 均有效。鲁索利替尼可成功替代 CNI 和大剂量激素。需要进一步研究以明确鲁索利替尼在 GVHD 治疗中的地位。