The major focus of this project is to evaluate and treat patients with malignant brain tumors. Treatment protocols are designed with the specific input of laboratory-based researchers. This clinical-laboratory interaction allows the rapid introduction of novel treatment strategies with the intended long-range goal of improved survival and quality of life for patients with primary malignant tumors of the central nervous system. Modalities of therapy will include surgery, gamma knife radiosurgery, interstitial brachytherapy, radiation therapy, radiosensitizers, chemotherapy, and gene therapy alone or in combination. The approach is multidisciplinary and includes the expertise of neurosurgeons, neuro- oncologists, neurologists, radiotherapists, medical oncologists, neuropathologists, clinical research nurses, and laboratory-based scientists. Protocols are jointly developed with clinical and laboratory researchers and the data captured and analyzed with the support of biostatiticians and data managers. For this renewal period, we will emphasize the use of radiation in the treatment of these patients. Protocols in progress or under development include randomized trials with interstitial brachytherapy and hyperthermia, the use of experimental radiosensitizers such as the halogenated pyrimidines and the polyamine inhibitors, treatment using altered fractionation schemes such as hyperfractionated radiotherapy and accelerated hyperfractionation, and radiosurgery using the gamma-knife. Adjuvant chemotherapy and phase II drug studies, including gene therapy, for recurrent tumors will also remain as an integral component of our total approach to the patient. Correlative data support for laboratory studies that are a part of this grant will come from clinical trials. Tumor and normal tissue stored in the tissue bank will serve as the source of material for other projects in this grant that will evaluate the radiosensitivity and molecular basis for radiation response. The clinical laboratory correlations that develop will serve as the substrate for newer, more individualized specific treatment recommendations for patients that will hopefully control disease with minimal or no toxicity.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA013525-25
Application #
6236083
Study Section
Project Start
1997-04-10
Project End
1998-03-31
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
25
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Rodriguez, Fausto J; Tihan, Tarik; Lin, Doris et al. (2014) Clinicopathologic features of pediatric oligodendrogliomas: a series of 50 patients. Am J Surg Pathol 38:1058-70
Chang, Susan M; Parney, Ian F; Huang, Wei et al. (2005) Patterns of care for adults with newly diagnosed malignant glioma. JAMA 293:557-64
Parney, Ian F; Kunwar, Sandeep; McDermott, Michael et al. (2005) Neuroradiographic changes following convection-enhanced delivery of the recombinant cytotoxin interleukin 13-PE38QQR for recurrent malignant glioma. J Neurosurg 102:267-75
Prados, Michael D; Seiferheld, Wendy; Sandler, Howard M et al. (2004) Phase III randomized study of radiotherapy plus procarbazine, lomustine, and vincristine with or without BUdR for treatment of anaplastic astrocytoma: final report of RTOG 9404. Int J Radiat Oncol Biol Phys 58:1147-52
Levin, Victor A; Hess, Kenneth R; Choucair, Ali et al. (2003) Phase III randomized study of postradiotherapy chemotherapy with combination alpha-difluoromethylornithine-PCV versus PCV for anaplastic gliomas. Clin Cancer Res 9:981-90
McKnight, Tracy R; von dem Bussche, Mary H; Vigneron, Daniel B et al. (2002) Histopathological validation of a three-dimensional magnetic resonance spectroscopy index as a predictor of tumor presence. J Neurosurg 97:794-802
Hamel, W; Zirkel, D; Mehdorn, H M et al. (2001) (E)-5-(2-bromovinyl)-2'-deoxyuridine potentiates ganciclovir-mediated cytotoxicity on herpes simplex virus-thymidine kinase--expressing cells. Cancer Gene Ther 8:388-96
Simmons, M L; Lamborn, K R; Takahashi, M et al. (2001) Analysis of complex relationships between age, p53, epidermal growth factor receptor, and survival in glioblastoma patients. Cancer Res 61:1122-8
Hamel, W; Dazin, P; Israel, M A (1996) Adaptation of a simple flow cytometric assay to identify different stages during apoptosis. Cytometry 25:173-81
Hamel, W; Magnelli, L; Chiarugi, V P et al. (1996) Herpes simplex virus thymidine kinase/ganciclovir-mediated apoptotic death of bystander cells. Cancer Res 56:2697-702

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