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NEUROONCOLOGY

$78,870U10FY2002CANIH

Mayo Clinic Coll Of Medicine, Rochester, Rochester MN

Investigators

Linked publications, trials & patents

Paper 39055377Paper 37539667Paper 36050448Paper 35859079Paper 34804634Paper 33154022Paper 32923882Paper 32504284Paper 31802506Paper 31213748Paper 30775161Paper 29848457Paper 29649081Paper 29530935Paper 29313954Paper 29164377Paper 29138761Paper 29044496Paper 28939223Paper 28921241Paper 28917648Paper 28786105Paper 28700816Paper 28691116Paper 28691057Paper 28687377Paper 28649983Paper 28646344Paper 28620884Paper 28533226Paper 28493308Paper 28402581Paper 28384065Paper 28375706Paper 28323331Paper 28280603Paper 28262692Paper 28239505Paper 28089762Paper 28006055Paper 27943153Paper 27881709Paper 27590208Paper 27534963Paper 27478689Paper 27468630Paper 27458945Paper 27374464Paper 27365012Paper 27302508Paper 27197192Paper 27098150Paper 27075674Paper 27060850Trial NCT01648348Trial NCT01369849Trial NCT01086605Trial NCT00869401Trial NCT00826540Trial NCT00738881Trial NCT00731731Trial NCT00699491Trial NCT00684983Trial NCT00641706Trial NCT00528645Trial NCT00459862Trial NCT00398112Trial NCT00369655Trial NCT00329719Trial NCT00321724Trial NCT00316849Trial NCT00255762Trial NCT00238394Trial NCT00238303Trial NCT00110084Trial NCT00109967Trial NCT00098540Trial NCT00096434Trial NCT00096070Trial NCT00093756Trial NCT00079274Trial NCT00079235Trial NCT00052949Trial NCT00052689Trial NCT00049127Trial NCT00039494Trial NCT00033267Trial NCT00027612Trial NCT00026234Trial NCT00026182Trial NCT00016328Trial NCT00015990Trial NCT00015821Trial NCT00014170Trial NCT00006226Trial NCT00005970Trial NCT00005036Trial NCT00003869Trial NCT00003140Patent 8507518

Abstract

The NCCTG Neuro-Oncology Program consists of three components: Cancer Treatment Trials, Neurobehavioral Studies, and Laboratory Correlates. These complementary components contribute to improving duration and quality of life in patients with primary central nervous system malignancies and to enhancing our understanding of the underlying disease process. During the previous grant cycle, in low-grade glioma patients, we observed that 65 cGy radiation is not better than 50 cGy; pro-carbazine, CCNU, grade glioma patients, we observed that 65 cGy radiation is not better than 50 cGy; procarbazine, CCNU, and vincristine (PCV) is an active regimen as initial therapy; and deletions in chromosomes 1p and 19q are associated with the diagnosis of low-grade oligodendrogliona, but not with low-grade oligoastrocytoma. In patients with high-grade glioma (glioblastoma multiforme, anaplastic oligoastrocytoma), we demonstrated that recombinant alpha interferon does not improve survival when added to radiation and BCNU, but is considerably more toxic; than grading (grade 3 versus grade 4) has significant prognostic value in patients with anaplastic oligoastrocytoma; and that, grade for grade, patients with anaplastic oligoastrocytoma have a statistically significant improved survival compared to those with pure astrocytoma. Moreover, tumoral EGFR amplification, absence of p53 mutations, and PTEN deletions are associated with poor survival in anaplastic astrocytoma patients. Glioblastoma and gliosarcoma patients have essentially identical clinical courses and genetic abnormalities. In recurrent glioma patients, we identified two active regimens: MOP (nitrogen mustard, vincristine, and procarbazine) and irinotecan. Ph. Pharmacokinetic studies demonstrated increase in CPT-11 clearance and variable metabolism in patients receiving irinotecal and anti-convulsants concurrently. Non-glioblastoma patients were more likely to respond to treatment than those with recurrent glioblastoma. Neurobehavioral studies indicated that good baseline Folstein and Folstein mini-mental status examination (MMSE) score is associated with better survival on multi-variate analyses. Few patients with high-grade glioma had diminished mini-mental examination scores at one year and 18 months in the absence of tumor progression. Conversely, reduction in mini-mental status examination scores correlated strongly with both at diagnosis, and were more likely to have cognitive decline to have cognitive decline as a consequence of treatment compared with younger patients. In patients with primary CNS lymphoma, we found a high response rate with CHOP (cyclophosphamide, doxorubicin, vincristine, and dexamethasone), but the duration of benefit was very short. As in patients with high-grade glioma, MMSE scores declined in close association with tumor progression. Future plans include continued evaluation of agents with radiosensitizing properties including cisplatin and irinotecan. We will continue to evaluate the efficacy of new regimens in recurrent glioma patients, including pyrazoloacridine plus carboplatin and the rapamycin analog, CCI 779. NCCTG has recruited investigators demonstrating experience with inhibitors of tumor invasion, as well as gene therapy. There are two main gene therapy approaches current in preclinical investigation: fusogenic membrane glycoproteins such as the measles virus F and H proteins and the truncated Gibbon Ape Leukemia virus surface protein (GALV). Neurobehavioral studies, including evaluation and treatment of impaired cognitive status, depression, fatigue, and excessive daytime somnolence, are in process. Pharmacokinetic studies to investigate interactions among chemotherapeutic agents and anti-convulsants will continue. Studies of genetic alterations in glioma, especially anaplastic astrocytoma and low- grade glioma, will be expanded through collaborations with Drs. Robert Jenkins (Mayo) David James (Mayo), and Bert Feuerstein (UCSF).

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