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

Publication ,  Journal Article
Houghton, PJ; Morton, CL; Tucker, C; Payne, D; Favours, E; Cole, C; Gorlick, R; Kolb, EA; Zhang, W; Lock, R; Carol, H; Tajbakhsh, M; Keir, ST ...
Published in: Pediatr Blood Cancer
December 2007

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.

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Published In

Pediatr Blood Cancer

DOI

ISSN

1545-5009

Publication Date

December 2007

Volume

49

Issue

7

Start / End Page

928 / 940

Location

United States

Related Subject Headings

  • Xenograft Model Antitumor Assays
  • Vincristine
  • Treatment Outcome
  • Oncology & Carcinogenesis
  • Neoplasms
  • Mice, SCID
  • Mice, Nude
  • Mice, Inbred NOD
  • Mice, Inbred BALB C
  • Mice
 

Citation

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Houghton, P. J., Morton, C. L., Tucker, C., Payne, D., Favours, E., Cole, C., … Smith, M. A. (2007). The pediatric preclinical testing program: description of models and early testing results. Pediatr Blood Cancer, 49(7), 928–940. https://doi.org/10.1002/pbc.21078
Houghton, Peter J., Christopher L. Morton, Chandra Tucker, Debbie Payne, Edward Favours, Claire Cole, Richard Gorlick, et al. “The pediatric preclinical testing program: description of models and early testing results.Pediatr Blood Cancer 49, no. 7 (December 2007): 928–40. https://doi.org/10.1002/pbc.21078.
Houghton PJ, Morton CL, Tucker C, Payne D, Favours E, Cole C, et al. The pediatric preclinical testing program: description of models and early testing results. Pediatr Blood Cancer. 2007 Dec;49(7):928–40.
Houghton, Peter J., et al. “The pediatric preclinical testing program: description of models and early testing results.Pediatr Blood Cancer, vol. 49, no. 7, Dec. 2007, pp. 928–40. Pubmed, doi:10.1002/pbc.21078.
Houghton PJ, Morton CL, Tucker C, Payne D, Favours E, Cole C, Gorlick R, Kolb EA, Zhang W, Lock R, Carol H, Tajbakhsh M, Reynolds CP, Maris JM, Courtright J, Keir ST, Friedman HS, Stopford C, Zeidner J, Wu J, Liu T, Billups CA, Khan J, Ansher S, Zhang J, Smith MA. The pediatric preclinical testing program: description of models and early testing results. Pediatr Blood Cancer. 2007 Dec;49(7):928–940.
Journal cover image

Published In

Pediatr Blood Cancer

DOI

ISSN

1545-5009

Publication Date

December 2007

Volume

49

Issue

7

Start / End Page

928 / 940

Location

United States

Related Subject Headings

  • Xenograft Model Antitumor Assays
  • Vincristine
  • Treatment Outcome
  • Oncology & Carcinogenesis
  • Neoplasms
  • Mice, SCID
  • Mice, Nude
  • Mice, Inbred NOD
  • Mice, Inbred BALB C
  • Mice