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醋酸奥曲肽在儿童中治疗化疗引起的腹泻是有效且安全的,但对急性移植物抗宿主病无效。

Octreotide acetate is efficacious and safe in children for treating diarrhea due to chemotherapy but not acute graft versus host disease.

机构信息

College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.

出版信息

Pediatr Blood Cancer. 2011 Jan;56(1):45-9. doi: 10.1002/pbc.22838.

Abstract

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.

摘要

背景

美国国立癌症研究所的常见毒性标准将腹泻评估为化疗给药的不良事件。急性移植物抗宿主病(aGVHD)会导致异基因造血干细胞移植患者腹泻。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。这些建议是基于成人奥曲肽试验得出的。关于奥曲肽治疗儿科肿瘤患者 CID 的使用数据有限。本研究评估了奥曲肽治疗儿科患者 CID 或 aGVHD 引起的腹泻的疗效和安全性。

方法

这是一项对 1994 年至 2008 年间接受奥曲肽治疗 CID 或 aGVHD 引起的腹泻的 34 名平均年龄为 6 岁的患者的回顾性研究。

结果

共给予 38 个疗程的静脉奥曲肽。25/27(92%)CID 和 5/11(45%)aGVHD 诱导的腹泻疗程中达到完全缓解。4/38 个疗程中达到部分缓解,均在 aGVHD 诱导的腹泻组中。aGVHD 诱导的腹泻 3 个疗程和 CID 1 个疗程无反应。奥曲肽起始剂量为 2 mcg/kg/天,最大剂量为 9 mcg/kg/天。治疗的平均总持续时间为 9 天。观察到的常见不良反应有高血糖、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 的有效率为 92%,治疗 aGVHD 诱导的腹泻的有效率为 45%。需要进一步研究以更好地确定治疗儿童 CID 的起始剂量和剂量递增算法。

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