We plan to continue to develop and assess the efficacy of novel approaches for the treatment of malignant disease based on studies in dogs with spontaneously occurring malignancies. Studies in dogs with malignant lymphoma have shown that some dogs treated with chemotherapy, total body irradiation (TBI) and autologous marrow infusion can be cured of their disease but that most will ultimately develop recurrent lymphoma. We propose to determine whether recurrent lymphoma results from infusion of malignant cells in the autologous marrow or from failure of TBI to eradicate all malignant cells. We will investigate the mechanism of cure in dogs free of disease after therapy by determining whether such dogs are immune to autologous lymphoma cells. We also plan to study the graft-versus-tumor effect of allogeneic marrow transplantation using a new immunosuppressive agent, cyclosporin A. In dogs with osteogenic sarcoma, we wish to test the hypothesis that growth of metastatic tumor can be inhibited by interference with hemostatic mechanisms. We also plan to assess whether the results of in vitro assays of cell-mediated and humoral immunity performed serially before and after amputation in dogs not given adjuvant chemotherapy correlate with in vivo events. We also will compare the effectiveness of conventional versus high dose methotrexate as cytoreductive chemotherapy administered before amputation. We also plan to study the feasibility and effectiveness of positron emission tomography in tumor imaging.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA018105-10
Application #
3164832
Study Section
Immunobiology Study Section (IMB)
Project Start
1975-12-01
Project End
1986-02-28
Budget Start
1984-12-01
Budget End
1986-02-28
Support Year
10
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
075524595
City
Seattle
State
WA
Country
United States
Zip Code
98109
Garrido, S M; Appelbaum, F R; Willman, C L et al. (2001) Acute myeloid leukemia cells are protected from spontaneous and drug-induced apoptosis by direct contact with a human bone marrow stromal cell line (HS-5). Exp Hematol 29:448-57
Garrido, S M; Cooper, J J; Appelbaum, F R et al. (2001) Blasts from elderly acute myeloid leukemia patients are characterized by low levels of culture- and drug-induced apoptosis. Leuk Res 25:23-32
Garrido, S M; Willman, C; Appelbaum, F R et al. (2000) Three-color versus four-color multiparameter cell cycle analyses of primary acute myeloid leukemia samples. Cytometry 42:83-94
Banker, D E; Radich, J; Becker, A et al. (1998) The t(8;21) translocation is not consistently associated with high Bcl-2 expression in de novo acute myeloid leukemias of adults. Clin Cancer Res 4:3051-62
Banker, D E; Groudine, M; Willman, C L et al. (1998) Cell cycle perturbations in acute myeloid leukemia samples following in vitro exposures to therapeutic agents. Leuk Res 22:221-39
Banker, D E; Groudine, M; Norwood, T et al. (1997) Measurement of spontaneous and therapeutic agent-induced apoptosis with BCL-2 protein expression in acute myeloid leukemia. Blood 89:243-55
Francisco, L V; Langston, A A; Mellersh, C S et al. (1996) A class of highly polymorphic tetranucleotide repeats for canine genetic mapping. Mamm Genome 7:359-62
Hong, D S; Huss, R; Beckham, C et al. (1995) Major histocompatibility complex class II-mediated inhibition of hemopoiesis in vitro and in vivo is abrogated by c-kit ligand. Transplant Proc 27:642-3
Huss, R; Hong, D S; Beckham, C et al. (1995) Ultrastructural localization of stem cell factor in canine marrow-derived stromal cells. Exp Hematol 23:33-40
Schwarzinger, I; Raff, R F; Flowers, M et al. (1994) Recipient-specific donor cytotoxic T lymphocytes enhance engraftment of unrelated, DLA non-identical canine marrow. Bone Marrow Transplant 13:303-9

Showing the most recent 10 out of 78 publications