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成功治疗儿童和年轻成年患者难治性胃肠道移植物抗宿主病的口服倍氯米松双丙酸酯:病例报告。

Successful treatment of intractable gastrointestinal tract graft-vs-host disease with oral beclomethasone dipropionate in pediatric and young adult patients: Case reports.

机构信息

Department of Pediatrics, Faculty of Medicine, University of Yamanashi, Chuo, Yamanashi, Japan,Department of Pediatric Surgery, Faculty of Medicine, University of Yamanashi, Chuo, Yamanashi, Japan,Department of Pharmacy, University of Yamanashi Hospital, Chuo, Yamanashi, Japan.

出版信息

Medicine (Baltimore). 2022 Mar 18;101(11). doi: 10.1097/MD.0000000000029054.

Abstract

RATIONALE

The gastrointestinal (GI) tract is a common target organ of graft-vs-host disease (GVHD) in hematopoietic stem cell transplantation (HSCT) patients, and GI tract GVHD is often resistant to standard treatments such as corticosteroids. Moreover, longterm use of systemic corticosteroids sometimes induces adverse events such as infection. Beclomethasone dipropionate (BDP) is a potent, topically active corticosteroid, which is metabolized to an active derivative in the intestinal mucosa. Oral BDP therapy is reportedly effective against GI tract GVHD in adult HSCT patients, but its efficacy and safety in pediatric patients remain undefined. Here, we report three pediatric and young adult cases who were treated with oral BDP.

PATIENT CONCERNS

Three (6-, 7-, and 18-year-old) patients developed stage 2 to 4 lower GI tract GVHD, which was resistant to standard immunosuppressive therapies.

DIAGNOSIS

Lower GI tract GVHD in these patients was histopathologically proven by endoscopic biopsy.

INTERVENTIONS

Oral administration of enteric-coated capsules of BDP (3-8 mg/day) was started for the treatment of lower GI tract GVHD.

OUTCOMES

With the introduction of oral BDP therapy, their GI tract symptoms promptly resolved (abdominal pain, within 3-7 days; diarrhea, within 2-3 weeks). Subsequently, systemic immunosuppressive agents such as corticosteroids and mycophenolate mofetil were successfully tapered off. During oral BDP therapy, although cytomegalovirus antigenemia and Acinetobacter Iwoffii sepsis developed in 2 cases, both were curable with conventional treatments. In a young adult case, concomitant BK virus-associated hemorrhagic cystitis resolved after oral BDP was introduced and systemic immunosuppressive agents were reduced. Transient growth restriction was observed in a pediatric case who was treated with oral BDP for approximately 300days.

LESSONS

Our experiences suggest that oral BDP therapy is an effective approach for GI tract GVHD that is resistant to standard immunosuppressive therapies. Of clinical importance, our case suggests the possibility that oral BDP therapy may improve the immunosuppressive condition in GI tract GVHD patients by contributing to the reduction of systemic immunosuppressive medications as a result of prompt improvement of GI tract GVHD symptoms.

摘要

背景

胃肠道(GI)是造血干细胞移植(HSCT)患者移植物抗宿主病(GVHD)的常见靶器官,GI 道 GVHD 对皮质类固醇等标准治疗通常具有抗性。此外,长期使用全身皮质类固醇有时会引起感染等不良反应。倍氯米松二丙酸酯(BDP)是一种强效、局部作用的皮质类固醇,在肠黏膜中代谢为活性衍生物。据报道,口服 BDP 治疗对成人 HSCT 患者的 GI 道 GVHD 有效,但在儿科患者中的疗效和安全性仍未确定。在这里,我们报告了三例接受口服 BDP 治疗的儿科和年轻成年患者。

关注点

三名(6、7 和 18 岁)患者出现 2 至 4 级下 GI 道 GVHD,对标准免疫抑制治疗有抗性。

诊断

这些患者的下 GI 道 GVHD 通过内镜活检得到组织病理学证实。

干预

开始口服肠溶胶囊 BDP(3-8mg/天)治疗下 GI 道 GVHD。

结果

口服 BDP 治疗开始后,他们的 GI 道症状迅速缓解(腹痛,3-7 天内;腹泻,2-3 周内)。随后,成功减少了全身性免疫抑制剂,如皮质类固醇和霉酚酸酯。在口服 BDP 治疗期间,尽管 2 例患者发生巨细胞病毒抗原血症和鲍曼不动杆菌败血症,但均通过常规治疗治愈。在一名年轻成年患者中,BK 病毒相关性出血性膀胱炎在引入口服 BDP 并减少全身免疫抑制剂后得到缓解。一名接受口服 BDP 治疗约 300 天的儿科患者出现短暂的生长受限。

经验教训

我们的经验表明,口服 BDP 治疗对标准免疫抑制治疗有抗性的 GI 道 GVHD 是一种有效的方法。从临床重要性来看,我们的病例表明,口服 BDP 治疗可能通过促进 GI 道 GVHD 症状的迅速改善,从而减少全身免疫抑制剂的使用,从而改善 GI 道 GVHD 患者的免疫抑制状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d0b/10684226/91f2eb8c909f/medi-101-e29054-g001.jpg

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