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Precision Delivery of Steroids as a Rescue Therapy for Gastrointestinal Graft-versus-Host Disease in Pediatric Stem Cell Transplant Recipients.精准递送类固醇作为儿科干细胞移植受者胃肠道移植物抗宿主病的挽救疗法
J Clin Med. 2023 Jun 23;12(13):4229. doi: 10.3390/jcm12134229.
2
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Mesenchymal stromal cells as treatment or prophylaxis for acute or chronic graft-versus-host disease in haematopoietic stem cell transplant (HSCT) recipients with a haematological condition.间充质基质细胞作为患有血液疾病的造血干细胞移植(HSCT)受者急性或慢性移植物抗宿主病的治疗或预防手段。
Cochrane Database Syst Rev. 2019 Jan 30;1(1):CD009768. doi: 10.1002/14651858.CD009768.pub2.

本文引用的文献

1
Case Series of Precision Delivery of Methylprednisolone in Pediatric Inflammatory Bowel Disease: Feasibility, Clinical Outcomes, and Identification of a Vasculitic Transcriptional Program.儿童炎症性肠病中甲基强的松龙精准给药的病例系列研究:可行性、临床结局及血管炎转录程序的鉴定
J Clin Med. 2023 Mar 20;12(6):2386. doi: 10.3390/jcm12062386.
2
Current status of clinical trials assessing mesenchymal stem cell therapy for graft versus host disease: a systematic review.评估间充质干细胞治疗移植物抗宿主病的临床试验现状:系统评价。
Stem Cell Res Ther. 2022 Mar 4;13(1):93. doi: 10.1186/s13287-022-02751-0.
3
Adolescent and young adult (AYA) versus pediatric patients with acute leukemia have a significantly increased risk of acute GVHD following unrelated donor (URD) stem cell transplantation (SCT): the Children's Oncology Group experience.与儿科患者相比,患有急性白血病的青少年和年轻成人(AYA)在接受无关供者(URD)干细胞移植(SCT)后发生急性移植物抗宿主病(GVHD)的风险显著增加:儿童肿瘤学组的经验。
Bone Marrow Transplant. 2022 Mar;57(3):445-452. doi: 10.1038/s41409-021-01558-6. Epub 2022 Jan 6.
4
Safety of pediatric cerebral angiography.儿童脑血管造影的安全性。
J Neurosurg Pediatr. 2021 Nov 5;29(2):192-199. doi: 10.3171/2021.8.PEDS21301. Print 2022 Feb 1.
5
Association of Oral Corticosteroid Bursts With Severe Adverse Events in Children.口腔皮质类固醇冲击治疗与儿童严重不良事件的关联。
JAMA Pediatr. 2021 Jul 1;175(7):723-729. doi: 10.1001/jamapediatrics.2021.0433.
6
Vedolizumab for Steroid Refractory Lower Gastrointestinal Tract Graft-Versus-Host Disease.维得利珠单抗治疗激素难治性下消化道移植物抗宿主病。
Transplant Cell Ther. 2021 Mar;27(3):272.e1-272.e5. doi: 10.1016/j.jtct.2020.12.011. Epub 2020 Dec 16.
7
Ruxolitinib for the treatment of steroid-refractory acute GVHD (REACH1): a multicenter, open-label phase 2 trial.芦可替尼治疗激素耐药性急性移植物抗宿主病(REACH1):一项多中心、开放标签的 2 期试验。
Blood. 2020 May 14;135(20):1739-1749. doi: 10.1182/blood.2020004823.
8
Prevention and Treatment of Acute Graft-versus-Host Disease in Children, Adolescents, and Young Adults.儿童、青少年和青年急性移植物抗宿主病的防治
Biol Blood Marrow Transplant. 2020 May;26(5):e101-e112. doi: 10.1016/j.bbmt.2020.01.004. Epub 2020 Jan 11.
9
Pediatric acute GVHD: clinical phenotype and response to upfront steroids.儿科急性移植物抗宿主病:临床表型与激素初始治疗反应
Bone Marrow Transplant. 2020 Jan;55(1):165-171. doi: 10.1038/s41409-019-0651-9. Epub 2019 Sep 2.
10
Vedolizumab trough level monitoring in inflammatory bowel disease: a state-of-the-art overview.炎症性肠病中维得利珠单抗谷浓度监测:最新综述。
BMC Med. 2019 May 8;17(1):89. doi: 10.1186/s12916-019-1323-8.

精准递送类固醇作为儿科干细胞移植受者胃肠道移植物抗宿主病的挽救疗法

Precision Delivery of Steroids as a Rescue Therapy for Gastrointestinal Graft-versus-Host Disease in Pediatric Stem Cell Transplant Recipients.

作者信息

Levitte Steven, Ganguly Abantika, Frolik Sophie, Guevara-Tique Alix A, Patel Shaini, Tadas Ann, Klein Orly, Shyr David, Agarwal-Hashmi Rajni, Beach Lynn, Callard Elizabeth, Weinacht Katja, Bertaina Alice, Thakor Avnesh S

机构信息

Interventional Radiology Innovation at Stanford (IRIS), 3155 Porter Drive, Palo Alto, CA 94304, USA.

Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Stanford University, Palo Alto, CA 94304, USA.

出版信息

J Clin Med. 2023 Jun 23;12(13):4229. doi: 10.3390/jcm12134229.

DOI:10.3390/jcm12134229
PMID:37445274
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10342730/
Abstract

Graft versus host disease (GVHD) is one of the most serious complications following stem cell transplant in children and is a major cause of morbidity and mortality. Corticosteroids remain the mainstay of treatment, and although a majority of children respond to systemic steroids, those refractory to or dependent upon corticosteroids suffer from complications secondary to long-term steroid administration. This problem has prompted consideration of steroid-sparing treatment strategies, although the time to clinical remission can be variable. Intraarterial corticosteroid delivery has been used in adults as a rescue therapy in steroid-resistant patients, but its use in children has been limited. We investigated the feasibility of intraarterial steroid administration into the bowel and/or liver in a cohort of six pediatric patients with acute GVHD. All patients successfully underwent treatment with no serious adverse effects. Five of five (100%) patients with gastrointestinal bleeding due to GVHD had rapid symptom improvement by 48 h, which was durable up to three weeks. Three of four (75%) patients with hepatic GVHD had improved cholestasis following intraarterial steroid administration. Our experience with this small cohort preliminarily demonstrated the feasibility and safety of intraarterial steroid administration in children with acute GVHD. This approach warrants consideration as a rescue therapy in steroid-refractory cases and as a "bridge" therapy for children with severe acute GVHD who are transitioning to steroid-sparing regimens.

摘要

移植物抗宿主病(GVHD)是儿童干细胞移植后最严重的并发症之一,也是发病和死亡的主要原因。皮质类固醇仍然是主要的治疗方法,虽然大多数儿童对全身用类固醇有反应,但那些对皮质类固醇难治或依赖的儿童会因长期使用类固醇而出现并发症。这个问题促使人们考虑采用节省类固醇的治疗策略,尽管临床缓解时间可能各不相同。动脉内给予皮质类固醇已在成人中用作类固醇抵抗患者的挽救治疗,但在儿童中的应用有限。我们调查了在一组6例急性GVHD儿科患者中,向肠道和/或肝脏动脉内给予类固醇的可行性。所有患者均成功接受治疗,无严重不良反应。5例因GVHD导致胃肠道出血的患者中有5例(100%)在48小时内症状迅速改善,且持续长达三周。4例肝GVHD患者中有3例(75%)在动脉内给予类固醇后胆汁淤积有所改善。我们对这个小队列的经验初步证明了动脉内给予类固醇在急性GVHD儿童中的可行性和安全性。这种方法值得作为类固醇难治病例的挽救治疗以及作为正在过渡到节省类固醇方案的重度急性GVHD儿童的“桥梁”治疗加以考虑。