FOUNDATION
home  
who & why
what do we do
contact details
how to help
membership  
sponsors
comments
BRAIN TUMOUR
warning signs
childhood brain tumour
what to do
tests
types
research
treatments & prognosis
INFORMATION
breaking news  
books
publications scientific
publications clinical
online support
WA support  
interstate support groups  
WA support group meetings  
Expo 2013  
Expo 2011  
Expo 2010  
STORIES
your story
FUNDRAISING
event photographs  
why help
donate  
bequest
 
Find us on Facebook

Linktrader links

   
Provide your support urgently

Donate now

James Crofts Hope Foundation Inc.

publications scientific

Breaking News - New Scientist - May 2010
Davis FG, Freels S, Grutsch J, et al. Survival rates in patients with primary malignant brain tumours stratified by patient age and tumour histological type: an analysis based on Surveillance, Epidemiology, and End Results (SEER) data, 1973-1991. J Neurosurg. 1998;88:1-10. 
The largest epidemiological study of brain tumours, sponsored by the Central Brain Tumour Registry of the United States (CBTRUS), a sister organization of the American Brain Tumour Association (ABTA), contains significant information on the current profile of primary malignant brain tumours. The study of over 20,000 patients with brain tumours covers 18 years during which the diagnosis and treatment of brain tumours evolved rapidly. Considerable improvements in survival rates between the years of 1973 to 1980 and the more recent era of 1986 to 1991 were noted for children and adults with medulloblastoma, as well as adults with astrocytoma (non-malignant) and oligodendroglioma. Glioblastoma multiforme continues to the most intractable brain tumours with little improvement in survival despite dramatic advances in diagnostic and surgical technology. 

Gately S, Soff GA, Brem S. The potential role of basic fibroblast growth factor in the transformation of cultured primary human foetal astrocytes and the proliferation of human glioma (U-87) cells. Neurosurgery. 1995;37:723-730. 
The switch to the malignant phenotype may be linked to the gene expression of specific oncogenes and growth factors. In animal models and in vitro experiments, basic fibroblast growth factor is linked with the proliferation, invasion, and angiogenesis response of malignant brain tumour cells. These data support the development of pharmacological compounds that suppress the expression or inhibit the action of these growth factors. 

Fernandez PM, Brem S. Malignant brain tumours in the elderly. Clin Geriatr Med. 1997;13:327-338. 
The increase in the incidence of primary brain tumours in the elderly over the last decade represents a serious health problem. Surgery remains the mainstay of the management of malignant gliomas, and the extent of the resection is one factor linked to the length of survival. This article reviews standard treatment modalities as well as novel approaches in clinical trials to treat newly diagnosed and recurrent glioblastomas. 

Brem S, Rozental JM, Moskal JR. What is the etiology of human brain tumours? A report on the first Lebow Conference. Cancer. 1995; 76:709-713. 
The key to the optimal treatment of brain tumours will be the clear understanding of the biological origins, preventable factors, and specific control mechanisms. The puzzle of what causes brain tumours remains complex with theories linking it to environmental (eg, electromagnetic radiation), genetic, dietary, and hereditary factors. The Lebow Conference, attended by prominent scientists and clinicians, identified new avenues of research across multiple scientific disciplines. 

Brem H, Piantadosi S, Burger PC, et al. Placebo-controlled trial of safety and efficacy of intraoperative controlled delivery by biodegradable polymers of chemotherapy for recurrent gliomas. Lancet. 1995; 345:1008-1012. 
This prospective, randomised, placebo-controlled, multicentre trial of 222 patients is noteworthy because it reports a new treatment that is safe and effective for recurrent malignant gliomas. The study was conducted under rigorous control and opens the door for further trials with more effective drugs. 

Harbaugh KS, Black PM. Strategies in the surgical management of malignant gliomas. Semin Surg Oncol. 1998;14:26-33. 
This article reviews the current neurosurgical technology including MRI guidance and stereotaxy to maximize the safe removal of the brain tumour while sparing "eloquent" and vital areas of brain. 

Fetell MR, Grossman SA, Fisher JD, et al. Pre-irradiation paclitaxel in glioblastoma multiforme: efficacy, pharmacology, and drug interactions. New Approaches to Brain Tumour Therapy Central Nervous System Consortium. J Clin Oncol. 1997;15:3121-3128. 
The plasma concentrations of paclitaxel in patients taking enzyme-inducing antiepileptic drugs (eg, diphenylhydantoin, carbamazepine, phenobarbital) were significantly lower than in patients not taking these antiseizure medication. Thus, the concomitant administration of antiseizure medication introduces an important variable in interpreting efficacy data, pharmacokinetics, and toxicity of novel agents for treatment of brain tumours. 

Lang FF, Sawaya R. Surgical treatment of metastatic brain tumours. Semin Surg Oncol. 1998; 14:53-63. 
This article provides a clear exposition of criteria for selection of suitable candidates for surgery, emphasizing that multiple or recurrent brain metastases can be successfully removed with an increase in survival and enhancement of the quality of life, often complementing other available modalities such as stereotactic radiosurgery and whole-brain irradiation. 

Jacobs W, Mikkelsen T, Smith R, et al. Inhibitory effects of CAI in glioblastoma growth and invasion. J Neurooncol. 1997;32:93-101. 
CAI, carboxyamide-triazole, is an anticancer agent developed as an inhibitor of selected signal transduction pathways. CAI inhibits the invasive phenotype of human glioma cell lines and decreases production of the 72kDa and 92 kDa type IV collagenases, thus suggesting a potential for benefit in the treatment of high-grade astrocytomas. 

Harsh GR 4th. Management of recurrent gliomas and meningiomas. In: Kaye AH, Laws ER Jr, eds. Brain Tumours: An Encyclopedic Approach. New York, NY: Churchill Livingstone; 1995:413-428. 
This report represents a superb overview of the multimodality treatment of gliomas in an outstanding reference source for the modern approach to brain tumours.

Back to top of page

 

Neuro Oncology Papers in Peer Review Journals

Guidelines and audit measures for good practice in the management of malignant cerebral glioma. Davies E, Hopkins A. Brit. J. Neurosurg. 11; 318-330,1997

Whittle I R, Simpson D A. Surgery for intracranial neonatal teratoma. Surg Neurol 15;268-273, 1981

Whittle I R, Foo M S, Vanderfield G K., Besser M. Progesterone and estrogen receptors in meningiomas. Clinical and biochemical considerations. Aust N Z J Surg 54; 325-330, 1984

Whittle I R, McLelland K, Martin F, Johnston I H. Unilateral retinoblastoma and concurrent pineoblastoma; A forme fruste of trilateral retinoblastoma? Neurosurgery 16; 500-505, 1985

Back to top of page