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儿科临床前测试项目:模型描述及早期测试结果

The pediatric preclinical testing program: description of models and early testing results.

作者信息

Houghton Peter J, Morton Christopher L, Tucker Chandra, Payne Debbie, Favours Edward, Cole Claire, Gorlick Richard, Kolb E Anders, Zhang Wendong, Lock Richard, Carol Hernan, Tajbakhsh Mimi, Reynolds C Patrick, Maris John M, Courtright Joshua, Keir Stephen T, Friedman Henry S, Stopford Charles, Zeidner Joseph, Wu Jianrong, Liu Tiebin, Billups Catherine A, Khan Javed, Ansher Sherry, Zhang Jian, Smith Malcolm A

机构信息

Department of Molecular Pharmacology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

出版信息

Pediatr Blood Cancer. 2007 Dec;49(7):928-40. doi: 10.1002/pbc.21078.

Abstract

BACKGROUND

The Pediatric Preclinical Testing Program (PPTP) is an initiative supported by the National Cancer Institute (NCI) to identify novel therapeutic agents that may have significant activity against childhood cancers. The PPTP has established panels of childhood cancer xenografts and cell lines to be used for in vivo and in vitro testing. These include panels for Wilms tumor, sarcomas (rhabdomyosarcoma, Ewing sarcoma, and osteosarcoma), neuroblastoma, brain tumors (glioblastoma, ependymoma, and medulloblastoma), rhabdoid tumors (CNS and renal), and acute lymphoblastic leukemia (ALL). Here, we describe the characteristics of the in vivo tumor panels and report results for the in vivo evaluation of two standard agents, vincristine and cyclophosphamide.

PROCEDURES

Solid tumors were grown subcutaneously in immune-deficient mice and tumor dimensions were measured weekly. ALL xenografts were inoculated intravenously and human CD45-positive cells were enumerated weekly.

RESULTS

Vincristine-induced objective responses in 6 of 24 (25%) and cyclophosphamide-induced objective responses in 18 of 28 (64%) solid tumor models. Comparable assessments of high levels of activity for these two agents were obtained using a tumor growth delay (TGD) measure. Both agents induced regressions in each of the ALL models evaluated.

CONCLUSIONS

We have established 51 solid tumor and 10 ALL in vivo models. The models identify vincristine and cyclophosphamide as having broad-spectrum activity. The PPTP tumor panels appear to generally recapitulate the activity of these agents against specific childhood cancers and to have the potential for identifying novel agents having significant clinical activity.

摘要

背景

儿科临床前测试项目(PPTP)是一项由美国国立癌症研究所(NCI)支持的计划,旨在识别可能对儿童癌症具有显著活性的新型治疗药物。PPTP已经建立了用于体内和体外测试的儿童癌症异种移植瘤和细胞系面板。这些包括肾母细胞瘤、肉瘤(横纹肌肉瘤、尤因肉瘤和骨肉瘤)、神经母细胞瘤、脑肿瘤(胶质母细胞瘤、室管膜瘤和髓母细胞瘤)、横纹肌样肿瘤(中枢神经系统和肾脏)以及急性淋巴细胞白血病(ALL)的面板。在此,我们描述了体内肿瘤面板的特征,并报告了两种标准药物长春新碱和环磷酰胺的体内评估结果。

程序

将实体瘤皮下接种到免疫缺陷小鼠体内,每周测量肿瘤大小。将ALL异种移植瘤静脉接种,并每周计数人CD45阳性细胞。

结果

长春新碱在24个实体瘤模型中的6个(25%)中诱导了客观反应,环磷酰胺在28个实体瘤模型中的18个(64%)中诱导了客观反应。使用肿瘤生长延迟(TGD)测量方法对这两种药物的高水平活性进行了可比评估。两种药物在每个评估的ALL模型中均诱导了肿瘤消退。

结论

我们建立了51个实体瘤和10个ALL体内模型。这些模型确定长春新碱和环磷酰胺具有广谱活性。PPTP肿瘤面板似乎总体上概括了这些药物对特定儿童癌症的活性,并具有识别具有显著临床活性的新型药物的潜力。

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