TY - JOUR
T1 - The pediatric preclinical testing program
T2 - Description of models and early testing results
AU - Houghton, Peter J.
AU - Morton, Christopher L.
AU - Tucker, Chandra
AU - Payne, Debbie
AU - Favours, Edward
AU - Cole, Claire
AU - Gorlick, Richard
AU - Kolb, E. Anders
AU - Zhang, Wendong
AU - Lock, Richard
AU - Carol, Hernan
AU - Tajbakhsh, Mimi
AU - Reynolds, C. Patrick
AU - Maris, John M.
AU - Courtright, Joshua
AU - Keir, Stephen T.
AU - Friedman, Henry S.
AU - Stopford, Charles
AU - Zeidner, Joseph
AU - Wu, Jianrong
AU - Liu, Tiebin
AU - Billups, Catherine A.
AU - Khan, Javed
AU - Ansher, Sherry
AU - Zhang, Jian
AU - Smith, Malcolm A.
PY - 2007/12
Y1 - 2007/12
N2 - 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.
AB - 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.
KW - Cyclophosphamide
KW - Developmental therapeutics
KW - Preclinical testing
KW - Vincristine
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U2 - 10.1002/pbc.21078
DO - 10.1002/pbc.21078
M3 - Article
C2 - 17066459
AN - SCOPUS:34447249881
VL - 49
SP - 928
EP - 940
IS - 7
ER -