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首页> 外文期刊>Pediatric blood & cancer >Octreotide acetate is efficacious and safe in children for treating diarrhea due to chemotherapy but not acute graft versus host disease.
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Octreotide acetate is efficacious and safe in children for treating diarrhea due to chemotherapy but not acute graft versus host disease.

机译:醋酸奥曲肽对儿童因化疗而引起的腹泻有效且安全,但对急性移植物抗宿主病无效。

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BACKGROUND: The Common Toxicity Criteria of the National Cancer Institute evaluates diarrhea as an adverse event of chemotherapy administration. Acute graft versus host disease (aGVHD) causes diarrhea in allogeneic hematopoietic stem cell transplant patients. Guidelines for treating grade 3 and 4 chemotherapy induced diarrhea (CID) include octreotide acetate, a somatostatin analogue. These recommendations are based on adult octreotide trials. Data on octreotide use for treatment of CID in pediatric oncology patients are limited. This study evaluated the efficacy and safety of octreotide in the treatment of CID or aGVHD induced diarrhea in pediatric patients. METHODS: This is a retrospective review of 34 patients of average age 6 years who received octreotide between 1994 and 2008 for treatment of CID or aGVHD induced diarrhea. RESULTS: Thirty-eight courses of intravenous octreotide were administered. A complete response was achieved during 25/27 (92%) CID and 5/11 (45%) aGVHD induced diarrhea courses. A partial response was achieved during 4/38 courses, all in the aGVHD induced diarrhea group. No response was observed for 3 of the aGVHD induced diarrhea courses and 1 for the CID course. Octreotide was initiated at 2 mcg/kg/day and increased to a maximum of 9 mcg/kg/day. The mean total duration of treatment was 9 days. Common adverse effects observed were hyperglycemia, hyberbilirubinemia, nausea/vomiting, and abdominal cramping. CONCLUSION: In pediatric patients, octreotide exhibits 92% efficacy in treating CID and 45% efficacy in aGVHD induced diarrhea. Further studies to better characterize the starting dose and dose escalation algorithm for treating CID in children are required.
机译:背景:美国国家癌症研究所的通用毒性标准将腹泻评估为化疗的不良反应。急性移植物抗宿主病(aGVHD)在异基因造血干细胞移植患者中引起腹泻。治疗3级和4级化疗引起的腹泻(CID)的指南包括醋酸奥曲肽,一种生长抑素类似物。这些建议基于成人奥曲肽试验。关于奥曲肽用于小儿肿瘤患者的CID治疗的数据有限。这项研究评估了奥曲肽治疗CID或aGVHD引起的小儿腹泻的疗效和安全性。方法:这是对1994年至2008年间接受CRE或aGVHD引起的腹泻治疗的平均年龄6岁的34例接受奥曲肽治疗的患者的回顾性回顾。结果:静脉注射奥曲肽共38个疗程。在25/27(92%)的CID和5/11(45%)的aGVHD诱导的腹泻过程中实现了完全缓解。在aGVHD引起的腹泻组中,全部4/38个疗程中均获得了部分缓解。对于3种由aGVHD引起的腹泻病程和1种CID病程,未观察到反应。奥曲肽的起始剂量为2 mcg / kg /天,最高增加到9 mcg / kg /天。平均总治疗时间为9天。观察到的常见不良反应是高血糖,高胆红素血症,恶心/呕吐和腹部绞痛。结论:在儿科患者中,奥曲肽治疗CID的疗效为92%,对aGVHD引起的腹泻的疗效为45%。需要进一步研究以更好地表征治疗儿童CID的起始剂量和剂量递增算法。

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