Excerpt:
By Shawn Le
The germ of the idea came to neurosurgeon Behnam Badie, M.D., over a meal with diabetes expert Samuel Rahbar, M.D., Ph.D.
“We would meet for lunch and I would ask about his career and research,” Badie said. “I learned a lot during those talks, especially about his discovery of hemoglobin A1c.”
Hemoglobin is the molecule that carries oxygen in red blood cells. Hemoglobin A1c is a special type of hemoglobin that has a form of sugar attached to it. “It is the standard risk measurement for complications in people with diabetes,” explained Badie, chief of the Division of Neurosurgery and director of the Brain Tumor Program.
Photo of Benham BadieNeurosurgeon and brain cancer researcher Benham Badie in the operating room. (©2005 Philip Channing)
Why would a neurosurgeon find diabetes research so fascinating? Because it might have implications for Badie’s own patients.
Their talks delved deeper into molecules studied by Rahbar, professor in the Department of Diabetes and Metabolic Diseases Research. These substances are called advanced glycation end products (AGEs).
In people with diabetes, too much sugar circulates and accumulates in the blood. AGEs form when this extra sugar binds to proteins and other molecules in the body.
These AGEs lie behind a lot of the complications of diabetes. AGEs can connect with receptors for advance glycation end products, or RAGE, much like a key fitting into a lock. This connection triggers inflammation and leads to conditions such as the deadening of nerve sensation and vision loss.
When other molecules activate RAGE, it can lead to other serious health conditions such as the narrowing of arteries, congestive heart failure and Alzheimer’s disease.
And, as it turns out, RAGE happens to be active around glioma, a brain cancer.
RAGE could be the common ground between diabetes and brain cancer
Tumor Suppressor Gene: Gene Function 'Lost' In Melanoma And Glioblastoma
ScienceDaily (2008-12-15) -- Researchers have found a gene they say is inactivated in two aggressive cancers -- malignant melanoma, a form of skin cancer, and glioblastoma multiforme, a lethal brain tumor. They add that because this gene, known as PTPRD, has recently been found to be inactivated in several other cancers as well, their discovery suggests that PTPRD may play a tumor suppressor role in a wide variety of different cancers.
Discovery offers way of tracking cancer in blood
By Julie Steenhuysen
CHICAGO (Reuters) - Tiny sacs released from tumor cells and circulating in the blood carry genetic information about the tumor, offering a new way to track and treat the cancer, U.S. researchers said on Sunday.
"They contain a little piece of the tumor cell in the blood stream. If you just look at these packets, you basically know what kind of mutations are in the tumor cell," said Xandra Breakefield of Massachusetts General Hospital in Boston, whose study appears in the journal Nature Cell Biology.
Tiny Sacs Released By Brain Tumor Cells Carry Information That May Guide Treatment
ScienceDaily (2008-11-17) -- Microvesicles - tiny membrane-covered sacs - released from glioblastoma cells contain molecules that may provide data that can guide treatment of the deadly brain tumor. Researchers have found tumor-associated RNA and proteins in membrane microvesicles called exosomes in blood samples from glioblastoma patients. Detailed analysis of exosome contents identified factors that could facilitate a tumor's growth through delivery of genetic information or proteins, or signify its vulnerability to particular medications.
Genentech seeks accelerated approval of drug to treat brain cancer
Genentech seeks accelerated approval of drug to treat brain cancer
Genentech today said it is seeking federal permission to have its cancer-fighting drug Avastin given accelerated approval to treat people with an aggressive form of brain cancer. The U.S. Food and Drug Administration already has approved Avastin for use in combination with chemotherapy to treat colon and breast cancer. In today's announcement, the South San Francisco biotechnology giant said it is seeking approval to have the drug approved to treat glioblastoma, the most common type of brain tumor.
Excerpt:
Whole Brain Radiation Not Best for Cancer That Has Spread
By Ed Edelson
HealthDay Reporter
Tuesday, September 23, 2008; 12:00 AM
TUESDAY, Sept. 23 (HealthDay News) -- The common practice of adding whole brain radiation to more focused radiation treatment for cancers that have spread to the brain not only caused greater learning and memory problems, but also was associated with a shorter survival time in a controlled study.
The survival time data should be approached with caution, because the primary purpose of the study was to help settle a debate about the effects of whole brain radiation on mental function, said study author Dr. Eric L. Chang, an associate professor of radiation oncology at M. D. Anderson Cancer Center in Houston. He presented the results Sept. 22 at the American Society for Therapeutic Radiology and Oncology annual meeting, in Boston.
But, he said, "this report will stimulate a lot of comment because of results we did not expect."
Family History Key Player in Brain Cancer Risk
Monday, September 22, 2008; 12:00 AM
MONDAY, Sept. 22 (HealthDay News) -- Having a family history of cancerous brain tumors puts you at a higher risk of developing the same kind of tumors, a new study says.
The research, published in the Sept. 23 issue ofNeurology, looked at the medical records and family histories of 1,401 people with either astrocytomas, tumors in the brain or spinal cord, or glioblastomas, a more aggressive and deadly category of astrocytomas.
Those whose immediate relatives had glioblastomas had twice the risk of also developing them. People with immediate relatives who had astrocytomas were nearly four times more likely to develop the same kind of tumor.
Getting Your Head Around Brain Cancer Understanding this complex disease and its treatment options
If you or someone you care about is one of the approximately 20,000 people in the United States diagnosed each year with a primary brain tumor,1 you should be encouraged as you fight this illness. The treatment options available today are providing more hope than ever before.
No one will argue that brain cancer remains a very complex disease: more than 120 different types of brain tumors have been identified, making an accurate diagnosis challenging; most brain tumors are not associated with any known risk factors, so they cannot currently be prevented; treatments are often risky due to potential damage to normal brain tissue; and prognosis depends on a multitude of factors, including tumor location and tumor type as well as patient age and personal health status.
But despite these challenges, diagnostic techniques and surgical technologies have dramatically improved in recent years, and ongoing research is paving the way for new and better treatments. Patients have reason to remain hopeful.
To help you or your loved one through the experience of brain cancer, it is essential to be knowledgeable about brain tumors and understand the treatment options.
Brain Tumor Types
Choosing the most appropriate treatment for a brain tumor depends on having the correct diagnosis. In general, brain tumors can be classified according to two major categories: the first is primary brain tumors, which begin in the brain and rarely spread to other parts of the body; the second is metastatic brain tumors, which begin as cancer in another part of the body (such as lung, breast, colon, kidney, or skin2,3) and spread to the brain. Metastatic brain tumors are the most common type, accounting for 160,000 diagnoses each year in the United States.
Primary Brain Tumors
Primary brain tumors are classified by how the cells behave (from the least aggressive, or benign, to the most aggressive, or malignant) and by the type of cell from which the tumor originates.
Tumor classification
Some tumor types are assigned a grade, which signifies the rate of growth. Grading is a determination of what stage, or how advanced, a tumor is in its development. The World Health Organization (WHO) classifies all cancers on a grade of I to IV, with a grade of I or II being slow growing and/or benign and III or IV being faster growing and/or malignant.5 Even though a brain tumor may be classified as benign, it still can be very dangerous if it is in a risky or inoperable location. The classification and the grade of a tumor help predict its behavior, but it is important to note that no two tumors are alike. Cellular makeup, speed of growth, location of tumor, and even the patient's age and immune system—all can affect tumor behavior, resulting in a variety of symptoms and different experiences among patients.6,7,8,9,10
Types of primary brain tumors
The most common type of primary brain tumor is a glioma, which originates in the brain from glial cells. Glial cells are the support cells of the central nervous system (CNS), helping neurons and nerve cells do their jobs. There are many types of gliomas11:
- Astrocytoma. The tumor arises from star-shaped glial cells called astrocytes. Astrocytes are cells that normally play an important role in maintaining the blood-brain barrier—the filtering mechanism that protects the brain. These tumors begin, when for reasons not completely known, a single astrocyte becomes abnormal. If that abnormal astrocyte multiplies, it will produce other astrocytes, eventually forming an astrocytoma.
- Glioblastoma multiforme (GBM). This is the most malignant astrocytoma (grade IV) and is the most common malignant brain tumor in adults.11
- Oligodendroglioma. This tumor type arises from cells that make the fatty substance that covers and protects nerves. They can be low-grade (WHO grade II) or anaplastic (WHO grade III), often contain calcifications, and are most common in middle-aged adults.12
- Ependymoma. The tumor arises from cells that line the central canal of the spinal cord. They are most commonly found in children and young adults.13
Some types of primary brain tumors do not begin in glial cells. These are the most common:
- Meningioma. This tumor occurs in the meninges and usually is slow growing. Meningiomas are quite common, accounting for about 25 percent of primary brain tumors and the majority of spinal cord tumors. They are almost twice as common in women than in men.14
- Vestibular schwannoma. This tumor arises from Schwann cells, which line the nerve in the inner ear that controls balance and hearing. The tumor, also called an acoustic neuroma, occurs most often in adults.
- CNS lymphoma. Lymphomas in the brain may be primary or secondary. Both are pathologically identical, and the diagnosis depends on whether another source of the lymphoma can be found elsewhere in the body. These tumors are initially very responsive to steroids, which can help in the diagnosis.15,16
- Sellar region tumors. These tumors, which include pituitary adenomas and craniopharyngiomas, grow at the base of the brain, near the pituitary gland, and are often associated with hormonal problems.
- Pineal region tumors. These rare brain tumors occur in or near the pineal gland, which is located between the cerebrum and the cerebellum.17
- Colloid cysts. These tumors classically occur in the third ventricle (a fluid-filled space in the brain) and can cause blockage of cerebrospinal fluid (CSF) flow. They are slow-growing, benign tumors, but there is a risk of sudden death due to CSF obstruction.18
- Medulloblastoma. This tumor is the most common brain tumor in children, accounting for 15 to 20 percent of pediatric brain tumors. This type usually arises in the midline of the cerebellum.19
Brain Tumor Treatment
Brain tumors can be challenging to treat, but many brain tumors can be successfully treated with one or more methods. In addition, new technology is enabling physicians to target tumors more precisely, and innovative treatments under investigation are offering hope for the future.
Deciding on an appropriate treatment regimen often requires the expertise of an entire medical team, as treatment depends on a number of factors, including the type, location, size, and grade of the tumor, as well as the overall health of the patient. It is important to work closely with your doctor so you feel comfortable with the treatment regimen recommended for you.
Surgery
The first line of treatment for a brain tumor is usually surgery, with the goal to remove as much of the tumor as possible without destroying normal function. Some tumors, such as meningiomas, schwannomas, and low-grade gliomas, may be treated by surgical removal alone or by surgery combined with radiation therapy.22 Tumors such as glioblastomas cannot be treated by surgery alone because cells from the tumor get too far into the normal surrounding brain tissue.23 In cases where the tumor is large and causing significant pressure, removal of the tumor can reduce symptoms such as headache, nausea, vomiting, and blurred vision. Surgery also can prolong life even if all of the tumor cannot be removed.24
Craniotomy
The most common type of surgery for diagnosis and treatment of brain tumors is a craniotomy, which involves the removal of a piece of the bone of the skull to access the tumor. There is growing data to suggest that more-complete surgical removal, whenever possible, is associated with a better prognosis.24,25
Surgical resection of a tumor is usually not recommended in the following cases:
- The tumor is too deep within the brain.
- The tumor is located in portions of the brain with important functions.
- The patient is unable to tolerate a major operation.
Shunt placement
Sometimes shunts are placed to bypass a blockage of the flow of cerebrospinal fluid. Without this bypass, a blockage can cause the fluid to build up within the brain (a condition known as hydrocephalus), leading to a life-threatening increase in pressure on vital parts of the brain.26
Radiation Therapy
Even after the most successful surgeries, residual microscopic tumor often remains, so additional treatment is needed to kill as many cells as possible. Radiation therapy uses high-energy X-rays or other types of ionizing radiation to stop cancer cells from dividing. It can be used when surgery is not advised, for tumors that cannot be completely removed, or after surgery to prevent or delay tumor recurrence.27
Radiation therapy can be delivered by internal or external means.
- Internal or interstitial radiation therapy (brachytherapy) involves surgically implanting radioactive material directly inside the tumor.28,29
- External beam radiation involves linear accelerators and cobalt machines that direct radiation at the tumor from outside the patient's body. There are two main types of external beam radiation:
- Conventional radiation therapy delivers radiation to an entire region of the brain. The radiation is fractionated into many small doses and given over a period of time. Depending on the location and the size of the tumor, the treatment can either be focused, where X-rays are aimed at the tumor and area surrounding it, or involve whole-brain radiation therapy (WBRT), whereby radiation is aimed at the entire brain. WBRT is used to treat multiple tumors and metastatic brain tumors.30
- Stereotactic radiosurgery delivers a single high dose of radiation in a one-day session. With the aid of computer imaging, the location of the tumor is accurately calculated and radiation is delivered directly to the tumor.31,32
The most common side effects of radiation are fatigue, nausea, loss of appetite, and short-term memory loss. Most of these symptoms can be treated or, in some cases, will decrease or disappear after treatment has been completed. Skin reactions (such as rash, redness, or irritation) and hair loss may occur in the area where the radiation is focused.
Systemic Chemotherapy
Chemotherapy is a cancer treatment that uses drugs to stop the growth of cancer cells, either by killing the cells or by stopping the cells from dividing. When chemotherapy is taken by mouth or injected into a vein or muscle, the drugs enter the bloodstream and can reach cancer cells throughout the body. Chemotherapy may be given alone or in combination with other treatments.
Treating brain tumors with systemic chemotherapy can be difficult because of the blood-brain barrier, which keeps out harmful substances such as bacteria and chemicals and can prevent some chemotherapy drugs from entering the brain. Researchers are currently testing drugs that may break through this barrier.33
Side effects of chemotherapy include hair loss, fatigue, mouth sores, easy bruising or bleeding, and lowered resistance to infection. Most side effects are temporary and go away after treatment is finished. If you have side effects, there are ways to ease their impact. For example, drugs can be given along with chemotherapy to prevent or reduce nausea and vomiting. Antibiotics can be given to prevent infection.
Some chemotherapy drugs can permanently damage certain organs and tissues such as the heart, kidneys, and nerves. These possible risks are carefully balanced against the benefits, and the health of these organs is carefully monitored during treatment. If serious organ damage occurs, the responsible drug is discontinued and replaced with another.
The most commonly used drugs are given orally, such as Temodar® (temozolomide)34,35 and CCNU (lomustine),36 or intravenously, such as BiCNU® (carmustine) and Camptosar® (CPT-11, (irinotecan).37
Chemotherapy Wafers
Another unique and effective way to deliver chemotherapy directly to brain tumors is through interstitial chemotherapy. With this method surgeons implant up to eight dime-sized Gliadel® Wafers—biodegradable wafers soaked with the chemotherapy drug BiCNU—directly into the brain after surgery. The chemotherapy wafers then release high concentrations of BiCNU locally over a period of two to three weeks; then they safely dissolve. Gliadel Wafers do not provide a cure for glioblastoma, but studies show that they may help keep some patients alive longer.38 The side effects associated with Gliadel Wafers are the same as those associated with surgery to remove the tumor. Current research focuses on combining these chemotherapy wafers with other therapies to increase their effectiveness.39 The wafers are also being studied for their merits in treating metastatic brain tumors,40 which affect thousands of women each year from solid tumor disease of the breast, lung, colon, kidney and skin.
Biologic Therapies
Researchers are currently designing drugs that identify and attack brain tumors on the molecular level, with the goal of destroying cancer cells while preserving healthy ones. Monoclonal antibodies, for example, that are tagged with a toxin or radiation can be loaded into an implantable reservoir and then placed in a cavity created during surgery. In principle, these antibodies are intended to seek and specifically destroy the "foreign" tumor cells for which they were designed.41,42
Growth Factor Inhibitors
A large number of malignant brain tumor cells carry on their surface an abnormally increased number of certain growth factor receptors. Researchers are studying drugs that block these receptors that signal tumors to grow. Tarceva® (erlotinib) and Iressa® (gefitinib) are two such drugs that target the epidermal growth factor receptor (EGFR) and have been shown to shrink tumors in some patients.43
Angiogenesis Inhibitors
Angiogenesis inhibitors, a group of drugs under investigation for treating brain tumors, interfere with the growth of blood vessels. Because brain tumors cannot grow without blood vessels to provide them with nourishment, the goal of angiogenesis inhibitors is to starve tumors of the nutrients and the oxygen they need to grow.44 Avastin® (bevacizumab) is an angiogenesis inhibitor that is currently being used in combination with cytotoxic chemotherapy drugs to treat brain cancer.
Immunotherapy and Cancer Vaccines
Immunotherapy attempts to make the body's own immune system more effective in finding and destroying cancer cells.45,46 Different techniques being studied to boost the immune system include cytokines (interferons and interleukins), which are created by the immune system and affect many different types of cells47; lymphocytes, which are cells that are able to fight cancer and can be grown in a laboratory and injected back into the tumor48; and tumor vaccines, which can be created from tumor cells that are removed, modified, and then transferred back to the patient.49,50
Gene Therapy
Another active area of research is the use of altered genes that will destroy tumor cells and shrink the size of a brain tumor while leaving healthy brain cells functional and unharmed. Usually, this genetic material is inserted into a virus and into liposomes, whose purpose is to serve as a delivery system. Clinical studies of gene therapy for brain tumors are still preliminary.51,52,53,54
Alternative Therapies
Many patients are seeing the benefit of complementary medical treatment—which includes specialties devoted to nutrition, exercise, acupuncture, aromatherapy, massage therapy, meditation, and yoga—to help relieve symptoms, minimize side effects, ease pain, and generally improve quality of life.55
Conclusion
Tremendous advancements have taken place in the battle against primary brain tumors, and promising treatments are on the horizon. The best way to prepare for this journey is to empower yourself through knowledge.
Resources
For additional information about treatment options for brain tumors, please visit the following Web sites:
www.abta.org American Brain Tumor Association
www.braintumor.org National Brain Tumor Foundation
www.cancerconsultants.com CancerConsultants.com
References
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47. Yang I, Kremen TJ, Giovannone AJ, et al. Modulation of major histocompatibility complex Class I molecules and major histocompatibility complex-bound immunogenic peptides induced by interferon-alpha and interferon-gamma treatment of human glioblastoma multiforme. Journal of Neurosurgery. 2004;100(2):310-19.
48. Kruse CA, Cepeda L, Owens B, Johnson SD, Stears J, Lillehei KO. Treatment of recurrent glioma with intracavitary alloreactive cytotoxic T lymphocytes and interleukin- 2. Cancer Immunology Immunotherapy. 1997;45(2):77-87.
49. Liau LM, Black KL, Martin NA, et al. Treatment of a patient by vaccination with autologous dendritic cells pulsed with allogeneic major histocompatibility complex class I-matched tumor peptides. Case Report. Neurosurgical Focus. 2000;9(6):e8.
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51. Rainov NG , Ren H. Clinical trials with retrovirus mediated gene therapy—what have we learned? Journal of Neuro-oncology. 2003;65(3):227-36. 52. Shah AC, Benos D, Gillespie GY, Markert JM. Oncolytic viruses: Clinical applications as vectors for the treatment of malignant gliomas. Journal of Neuro-oncology. 2003;65(3):203-26.
53. Vecil GG , Lang FF. Clinical trials of adenoviruses in brain tumors: A review of Ad-p53 and oncolytic adenoviruses. Journal of Neuro-oncology. 2003;65(3):237-46.
54. Yoshida J, Mizuno M. Clinical gene therapy for brain tumors. Liposomal delivery of anticancer molecule to glioma. Journal of Neuro-oncology. 2003;65(3):261-67.
55. Brain and Spinal Cord Tumors in Adults. American Cancer Society Web site. Available at: www.cancer.org/103.00/103.00.pdf. Accessed January 8, 2008.
56. Brain Tumor Facts & Statistics. Brain Tumor Society Web site. Available at: www. tbts.org/itemDetail.asp?categoryID=384&itemID=16535. Accessed January 8, 2008.
Massive gene scan finds brain tumor clues
Excerpt:
Posted by Elizabeth Cooney September 4, 2008 02:18 PM
A sweeping survey of cancer genes has turned up previously unknown mutations that lead to brain cancer and possibly explain resistance to a common chemotherapy drug used to treat it, Boston researchers from a multi-center team report. A paper appearing in Nature describes a systematic analysis of 206 glioblastoma multiforme tumors, the kind of cancer that Senator Edward M. Kennedy has. The gene search results come from the Cancer Genome Atlas Research Network, a $100 million pilot project funded by the National Institutes of Health to test this kind of large-scale systematic approach to cancer research.
The gene survey confirmed five mutations already identified in brain tumors and found three new ones. The researchers also tracked disruptions in cellular function that the mutations led to, including problems with cell division, cell growth, and repair of DNA damage.
Interesting Excerpt
Dog treated for brain tumors: Experimental test a trial for humans
If it works for ‘Batman’ and other dogs, it promises effective treatment, say Minneapolis researchers
Star Tribune (Minneapolis)
Thursday, August 21, 2008
MINNEAPOLIS — Batman has always been a hero to Anna and Eric Baker. Not the comic book variety, but a furry, 38-pound, bat-eared one who patiently lets their toddler climb all over him.
Now, if all goes well, he may also become a hero for the thousands of people — and tens of thousands of dogs — who each year have brain tumors diagnosed that are equally fatal in both.
Batman, a Shepard mix, is having surgery to remove a brain tumor, August 5, 2008, at the University of Minnesota’s Veterinary Medical Center. It’s the same kind of tumor that is common in people. Cancer researchers will use his surgery for an experimental advanced treatment.
Scorpion Venom May Help Treat Brain Cancer
Chemical May One Day Be Used to Seek Out, 'Paint' Brain Tumors
By DAN CHILDS
ABC News Medical Unit
Aug. 11, 2008—
The sting of the Giant Yellow Israeli Scorpion packs a painful punch. Its venom contains a potent cocktail of neurotoxins that places an animal or human victim in excruciating agony.
It's not the first place most would think to look for a weapon against cancer. But doctors and researchers report that a particular component within this dangerous mix may be able to seek out brain tumor cells. And one researcher, as reported by ABC affiliate KOMO-TV in Seattle, hope that doctors will one day be able to use this property to "paint" tumors for a surgeons to see.
"Right now it is difficult for a surgeon to be able to distinguish a brain tumor from the normal brain tissue around it," says Dr. James Olson of the Fred Hutchinson Cancer Research Center. He says that this situation often presents today's brain surgeon with an unenviable decision: choose either to cut aggressively, potentially damaging healthy brain tissue, or cut conservatively and run the risk of leaving tumor cells behind.
Enter T-601, the synthetic version of a chemical first found in the scorpion's sting. Neurobiologist Harold Sontheimer of the University of Alabama at Birmingham, who was the first to explore the medical potential of this chemical, found that it was able to pass into the brain unobstructed. That's a feat for most chemicals, as the membrane that separates the brain from the bloodstream (known as the blood-brain barrier) is notoriously impermeable.
Is This Realistic for the Average Person Diagnosed with Brain Cancer
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The story behind Kennedy's brain surgery
What is known is that a few days after Kennedy learned he had a malignant brain tumor in the left parietal lobe, he invited a group of national experts to discuss his case.
The meeting on May 30 was extraordinary in at least two ways.
One was the ability of a powerful patient — in this case, a scion of a legendary political family and the chairman of the Senate’s health committee — to summon noted consultants to learn about the latest therapy and research findings.
The second was his efficiency in quickly convening more than a dozen experts from at least six academic centers. Some flew to Boston. Others participated by telephone after receiving pertinent test results and other medical records.
