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小儿肉瘤的伊立替康治疗十五年:下一步何去何从?

Fifteen years of irinotecan therapy for pediatric sarcoma: where to next?

作者信息

Wagner Lars M

机构信息

Division of Pediatric Hematology/Oncology, Kentucky Clinic Suite, University of Kentucky, J-457, Lexington, KY 40536 USA.

出版信息

Clin Sarcoma Res. 2015 Aug 28;5:20. doi: 10.1186/s13569-015-0035-x. eCollection 2015.

DOI:10.1186/s13569-015-0035-x
PMID:26322224
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4552408/
Abstract

Over the past 15 years, irinotecan has emerged as an important agent for treating pediatric sarcoma patients. This review summarizes the activity noted in previous studies, and outlines current issues regarding scheduling, route of administration, and amelioration of side effects. Also discussed are new pegylated and nanoliposomal formulations of irinotecan and its active metabolite, SN-38, as well as future plans for how irinotecan may be used in combination with other conventional cytotoxic as well as targeted agents.

摘要

在过去15年里,伊立替康已成为治疗小儿肉瘤患者的一种重要药物。本综述总结了既往研究中观察到的活性,并概述了关于给药方案、给药途径和副作用改善方面的当前问题。还讨论了伊立替康及其活性代谢产物SN-38的新型聚乙二醇化和纳米脂质体制剂,以及伊立替康与其他传统细胞毒性药物和靶向药物联合使用的未来计划。

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本文引用的文献

1
Activity of MM-398, nanoliposomal irinotecan (nal-IRI), in Ewing's family tumor xenografts is associated with high exposure of tumor to drug and high SLFN11 expression.MM-398(纳米脂质体伊立替康,nal-IRI)在尤文氏家族肿瘤异种移植物中的活性与药物对肿瘤的高暴露和高 SLFN11 表达有关。
Clin Cancer Res. 2015 Mar 1;21(5):1139-50. doi: 10.1158/1078-0432.CCR-14-1882.
2
Synergistic activity of PARP inhibition by talazoparib (BMN 673) with temozolomide in pediatric cancer models in the pediatric preclinical testing program.在儿科临床前测试项目的儿科癌症模型中,他拉唑帕尼(BMN 673)与替莫唑胺联合抑制PARP的协同活性。
Clin Cancer Res. 2015 Feb 15;21(4):819-32. doi: 10.1158/1078-0432.CCR-14-2572. Epub 2014 Dec 10.
3
Targeting the DNA repair pathway in Ewing sarcoma.靶向尤因肉瘤中的DNA修复途径。
Cell Rep. 2014 Nov 6;9(3):829-41. doi: 10.1016/j.celrep.2014.09.028. Epub 2014 Oct 23.
4
Phase II study of olaparib in patients with refractory Ewing sarcoma following failure of standard chemotherapy.奥拉帕利用于标准化疗失败后的难治性尤因肉瘤患者的II期研究。
BMC Cancer. 2014 Nov 5;14:813. doi: 10.1186/1471-2407-14-813.
5
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Cancer Res. 2014 Dec 1;74(23):7003-13. doi: 10.1158/0008-5472.CAN-14-0572. Epub 2014 Oct 1.
6
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