Importance of dose intensity in neuro-oncology clinical trials: summary report of the Sixth Annual Meeting of the Blood-Brain Barrier Disruption Consortium
- PMID: 11305417
- PMCID: PMC1920598
- DOI: 10.1093/neuonc/3.1.46
Importance of dose intensity in neuro-oncology clinical trials: summary report of the Sixth Annual Meeting of the Blood-Brain Barrier Disruption Consortium
Abstract
Therapeutic options for the treatment of malignant brain tumors have been limited, in part, because of the presence of the blood-brain barrier. For this reason, the Sixth Annual Meeting of the Blood-Brain Barrier Disruption Consortium, the focus of which was the "Importance of Dose Intensity in Neuro-Oncology Clinical Trials," was convened in April 2000, at Government Camp, Mount Hood, Oregon. This meeting, which was supported by the National Cancer Institute, the National Institute of Neurological Disorders and Stroke, and the National Institute of Deafness and Other Communication Disorders, brought together clinicians and basic scientists from across the U.S. to discuss the role of dose intensity and enhanced chemotherapy delivery in the treatment of malignant brain tumors and to design multicenter clinical trials. Optimizing chemotherapy delivery to the CNS is crucial, particularly in view of recent progress identifying certain brain tumors as chemosensitive. The discovery that specific constellations of genetic alterations can predict which tumors are chemoresponsive, and can therefore more accurately predict prognosis, has important implications for delivery of intensive, effective chemotherapy regimens with acceptable toxicities. This report summarizes the discussions, future directions, and key questions regarding dose-intensive treatment of primary CNS lymphoma, CNS relapse of systemic non-Hodgkin's lymphoma, anaplastic oligodendroglioma, high-grade glioma, and metastatic cancer of the brain. The promising role of cytoenhancers and chemoprotectants as part of dose-intensive regimens for chemosensitive brain tumors and development of improved gene therapies for malignant gliomas are discussed.
Similar articles
-
Targeted delivery in primary and metastatic brain tumors: summary report of the seventh annual meeting of the Blood-Brain Barrier Disruption Consortium.Clin Cancer Res. 2002 Jun;8(6):1702-9. Clin Cancer Res. 2002. PMID: 12060607
-
Salvage therapy for primary CNS lymphoma with a combination of rituximab and temozolomide.Neurology. 2005 Mar 8;64(5):934; author reply 934. doi: 10.1212/wnl.64.5.934. Neurology. 2005. PMID: 15753455 No abstract available.
-
New frontiers in translational research in neuro-oncology and the blood-brain barrier: report of the tenth annual Blood-Brain Barrier Disruption Consortium Meeting.Clin Cancer Res. 2005 Jan 15;11(2 Pt 1):421-8. Clin Cancer Res. 2005. PMID: 15701824
-
Outwitting the blood-brain barrier for therapeutic purposes: osmotic opening and other means.Neurosurgery. 1998 May;42(5):1083-99; discussion 1099-100. doi: 10.1097/00006123-199805000-00082. Neurosurgery. 1998. PMID: 9588554 Review.
-
[Role of high-dose chemotherapy with hemopoietic stem-cell support in the treatment of adult patients with high-grade glioma].Bull Cancer. 2001 Sep;88(9):871-6. Bull Cancer. 2001. PMID: 11604360 Review. French.
Cited by
-
Honokiol traverses the blood-brain barrier and induces apoptosis of neuroblastoma cells via an intrinsic bax-mitochondrion-cytochrome c-caspase protease pathway.Neuro Oncol. 2012 Mar;14(3):302-14. doi: 10.1093/neuonc/nor217. Epub 2012 Jan 18. Neuro Oncol. 2012. PMID: 22259050 Free PMC article.
-
Effects of irradiation on brain vasculature using an in situ tumor model.Int J Radiat Oncol Biol Phys. 2012 Mar 1;82(3):1075-82. doi: 10.1016/j.ijrobp.2011.06.1984. Epub 2011 Dec 22. Int J Radiat Oncol Biol Phys. 2012. PMID: 22197233 Free PMC article.
-
Chemotherapeutic dose intensification for treatment of malignant brain tumors: recent developments and future directions.Curr Neurol Neurosci Rep. 2002 May;2(3):216-24. doi: 10.1007/s11910-002-0080-8. Curr Neurol Neurosci Rep. 2002. PMID: 11937000 Review.
-
Real-time monitoring of human blood-brain barrier disruption.PLoS One. 2017 Mar 20;12(3):e0174072. doi: 10.1371/journal.pone.0174072. eCollection 2017. PLoS One. 2017. PMID: 28319185 Free PMC article.
-
A phase II trial of a multi-agent oral antiangiogenic (metronomic) regimen in children with recurrent or progressive cancer.Pediatr Blood Cancer. 2014 Apr;61(4):636-42. doi: 10.1002/pbc.24794. Epub 2013 Oct 4. Pediatr Blood Cancer. 2014. PMID: 24123865 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous