[Treatment algorithm for gastrointestinal graft-versus-host disease].

G B McDonald
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Abstract

Over the last decade, there has been a dramatic decline in the frequency of organ failure, infection, and severe acute CVHD as causes of non-relapse mortality after allogeneic hematopoietic cell transplantation. Gastrointestinal CVHD, however, remains a significant obstacle to survival. Patients who present with non-progressive symptoms of the upper gut phenotype of GVHD seldom progress to severe CVHD, but may have a prolonged course, they can be successfully treated with prednisone 1 mg/kg/day for a limited time, along with topical and oral glucocorticoid. Patients who present with the mid-gut phenotype of GVHD can be recognized soon after presentation by secretory protein-losing enteropathy and falling serum albumin; their treatment requires prednisone 2 mg/kg/day and probably an additional drug such as mycophenolic acid. Failure to improve identifies a cohort with a poor prognosis; secondary therapy should be started while gut mucosa is still intact, but no secondary therapies have been proven in randomized trials to improve survival. Patients whose initial presentation (large volume diarrhea, low serum albumin, jaundice, mucosal necrosis and sloughing at initial endoscopy) presages a fatal outcome have not been studied prospectively.

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[胃肠道移植物抗宿主病的治疗算法]。
在过去的十年中,器官衰竭、感染和严重急性CVHD的频率急剧下降,这些原因是同种异体造血细胞移植后非复发性死亡的原因。然而,胃肠道CVHD仍然是生存的重大障碍。出现GVHD上肠表型非进行性症状的患者很少进展为严重的CVHD,但可能有一个延长的病程,他们可以用强的松1 mg/kg/天在有限的时间内成功治疗,同时局部和口服糖皮质激素。出现GVHD中肠表型的患者可以在出现后不久通过分泌性蛋白丢失性肠病和血清白蛋白下降来识别;他们的治疗需要强的松2毫克/公斤/天,可能还需要一种额外的药物,如霉酚酸。未能改善可确定预后不良的队列;二次治疗应在肠黏膜完好时开始,但在随机试验中没有证实二次治疗可以提高生存率。那些最初表现(大量腹泻、低血清白蛋白、黄疸、粘膜坏死和初次内窥镜检查时的脱落)预示致命结局的患者尚未进行前瞻性研究。
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