The pediatric preclinical testing program: Description of models and early testing results

被引:373
作者
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
[1] St Jude Childrens Res Hosp, Dept Mol Pharmacol, Memphis, TN 38105 USA
[2] Childrens Hosp Montefiore, Bronx, NY USA
[3] Childrens Canc Inst Australia Med Res, Randwick, NSW, Australia
[4] Childrens Hosp Los Angeles, Los Angeles, CA 90027 USA
[5] Univ Penn, Sch Med, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[6] Abraham Family Canc Res Inst, Philadelphia, PA USA
[7] NCI, Pediat Oncol Branch, Oncogen Sect, Bethesda, MD 20892 USA
[8] Duke Univ, Med Ctr, Durham, NC USA
[9] NCI, Canc Therapy Evaluat Program, Bethesda, MD 20892 USA
关键词
cyclophosphamide; developmental therapeutics; preclinical testing; vincristine;
D O I
10.1002/pbc.21078
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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%0) 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.
引用
收藏
页码:928 / 940
页数:13
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