Radiation therapy may be used alone or in combination with surgery and/or chemotherapy in the treatment of primary or metastatic brain cancers, which are also called brain tumors.
External beam radiation therapy (EBRT) is the conventional technique for administering radiation therapy to the brain, but stereotactic radiosurgery has also become a standard treatment. The most recent advance in the radiation treatment of brain tumors is the brachytherapy technique called GliaSite radiotherapy system, which involves placing a balloon in or near the tumor during surgery and then passing a radioactive material into the balloon for treatment.
The following is a general overview of radiation therapy for brain tumors. In some cases, participation in a clinical trial utilizing new, innovative radiation techniques may provide the most promising treatment. The potential benefits of combination treatment, participation in a clinical trial, or standard treatment must be carefully balanced with the potential risks. The information on this website is intended to help educate patients about their treatment options and to facilitate a mutual or shared decision-making process with their treating cancer physician.
- Techniques for Delivering Radiation Therapy to Brain Tumors
- External beam radiation therapy (EBRT)
- Stereotactic radiation therapy (SRT)
- Internal radiation therapy (brachytherapy)
- Procedures for Delivering Radiation Therapy to Brain Tumors
- Treatment Schedules
- Retreatment with radiation
- Side Effects and Complications of Radiation Therapy for Brain Tumors
- Strategies to Improve Radiation Therapy for Brain Tumors
The three primary techniques for delivering radiation therapy—external, internal, and stereotactic—have each been evaluated in the treatment of patients with brain tumors and may be utilized in different circumstances. While EBRT is the conventional treatment for brain tumors, SRT has also become a standard procedure. SRT has been used in the treatment of many types of brain tumors and been proven effective in the treatment of brain metastases. A recent advance in brachytherapy includes the FDA-approved GliaSite® radiation therapy system that involves passing a radioactive material into an implanted balloon.
External Beam Radiation Therapy (EBRT)
EBRT involves directing radiation beams from outside the body into the tumor. Machines called linear accelerators produce the high-energy radiation beams that penetrate the tissues and deliver the radiation dose directly to the cancer. These modern machines and other state-of-the-art techniques have enabled radiation oncologists to significantly reduce side effects while improving the ability to deliver radiation directly to the tumor.
EBRT is typically delivered as an outpatient procedure for approximately six to eight weeks. EBRT begins with a planning session, or simulation, during which the radiation oncologist places marks on the body and takes measurements in order to line up the radiation beam in the correct position for each treatment. During treatment, the patient lies on a table and the radiation is delivered from multiple directions. The actual area receiving radiation treatment may be large or small, depending on the features of the cancer. Radiation can be delivered to one specific area or encompass the surrounding tissues, including the lymph nodes.
Recent studies have demonstrated that whole brain radiation therapy (WBRT) is associated with greater side effects without improvements in control of the cancer when compared to SRT in individuals with limited metastatic cancer to the brain. Cognitive decline was more frequent with WBRT-SRT treatment when compared to SRT alone without a corresponding improvement in control of the cancer or overall survival. Although WBRT may be necessary for widespread cancer in the brain more targeted approaches appear superior when they can be appropriately utilized.1
Three-dimensional conformal radiation therapy (3D-CRT): EBRT can be delivered more precisely with the help of a special scan and a computer. The scan is called computed tomography (CT scan) and is used to identify the cancer “target.” The computer is used to “conform” the radiation to the tumor shape. This technique is known as three-dimensional conformal radiation therapy, or 3D-CRT. The use of 3D-CRT appears to reduce the chance of injury to nearby normal tissues. Since 3D-CRT can better target the area of cancer, radiation oncologists are evaluating whether higher doses of radiation can be given safely and provide more chances for cure.
Researchers have evaluated 3D-CRT in the treatment of patients with high-grade gliomas. In a clinical trial involving 34 patients treated with 3D-CRT, patients lived an average of 11.7 months. Nearly half of the patients lived one year or more after treatment and approximately 13% lived two years or more.2
High-dose 3D-CRT has been shown to increase survival compared to conventional radiation therapy. Researchers from Japan have reported that high-dose conformal radiation therapy improves survival for patients with anaplastic astrocytoma and glioblastoma compared to standard doses without increasing disabilities associated with radiation to the brain. Among 184 patients who were treated with high-dose conformal radiation, more than half (51%) survived five years or more compared to 15% of patients who had been treated with conventional radiation therapy.3
EBRT may be used to deliver radiation therapy to a part of the brain or the whole-brain. Whole-brain radiation therapy is usually recommended for a large or spreading brain tumor.
Proton radiation therapy: Proton radiation therapy is a form of EBRT that utilizes a beam of protons as the source of radiation rather than X-rays or gamma rays. Protons are released from atoms using technology similar to that employed in nuclear reactors. Computer-programmed blocks are precisely placed to direct the proton beam toward the tumor and match it to the shape of the tumor.
As a source of radiation, proton beams offer some advantages. In particular, a proton beam delivers a high dose of radiation to the tumor, but very little radiation affects normal tissue in front of and beside the tumor, and no radiation is deposited in the normal tissue behind the tumor. In this way, healthy brain tissue is spared from radiation damage. Standard EBRT beams may deposit much of their dose in tissues in front of the tumor, causing damage to normal tissue and associated side effects.
Proton radiation therapy may have a role in the treatment of unusually shaped tumors and small tumors that are located deep in the skull, such as skull base tumors or pituitary tumors. Proton radiation therapy has been evaluated in the treatment of meningiomas and appears to be effective. In a clinical trial involving 16 patients with intracranial meningiomas, over 90% survived free of cancer progression for three years or longer.4
Stereotactic Radiation Therapy (Gamma Knife Therapy)
Stereotactic radiation therapy (SRT) is a noninvasive approach to the treatment of brain tumors that uses pencil-thin beams of radiation to treat only the tumor. SRT uses imaging techniques—including CT scans or MRI—and special computerized planning to precisely focus a high dose of radiation on the brain tumor, while sparing normal tissue. This focused technique allows radiation to be delivered in an area of the brain or spinal cord that might be considered inoperable, and can be delivered to tumors that are one and one-half inches in diameter or smaller. Another major advantage to SRT is that radiation treatment is delivered in a single session.
SRT has become a standard treatment for primary and metastatic brain tumors and may be delivered as:
- An addition to conventional EBRT, called local “boost” radiation, when the patient has already received the maximum safe dose of conventional radiation therapy,
- The only technique used to deliver radiation therapy to some brain tumors, or
- A substitute for surgery for a metastatic brain tumor or a benign tumor (such as a pituitary, pineal region, or acoustic tumor).
Prior to SRT, the patient is fitted with a head frame. CT and/or MRI scans are performed with the head frame in place to locate the tumor and obtain information necessary for computerized treatment planning. Treatment is totally non-invasive and painless. Patients maintain their normal function and are completely awake and alert throughout the entire procedure.
Possible side effects of SRT include edema (swelling), occasional neurological problems, and radiation necrosis (an accumulation of dead cells). A second surgery to remove the build-up of dead tumor cells may be required.
Types of Stereotactic Radiosurgery Equipment
Two types of machines are used routinely to deliver SRT: Gamma Knife® and linear accelerators (LINAC).
Gamma Knife: The Gamma Knife is an instrument that was developed by researchers in Sweden nearly three decades ago. It delivers 201 beams of radiation that are focused by a computer so that they intersect at the precise location of the cancer. The patient is placed on a couch and then a large helmet is attached to the head frame. Holes in the helmet allow the beams to match the calculated shape of the tumor.
The most frequent use of the Gamma Knife has been for small, benign tumors, particularly acoustic neuromas, meningiomas, and pituitary tumors. For larger tumors, partial surgical removal might be required first. The Gamma Knife is also used to treat solitary metastases and small malignant tumors with well-defined borders.
LINAC: An adapted linear accelerator can deliver a single, high-energy beam that is computer-shaped to the tumor. The patient is positioned on a sliding bed around which the linear accelerator circles. The linear accelerator directs arcs of radioactive photon beams at the tumor. The pattern of the arc is computer-matched to the tumor’s shape. This reduces the dose delivered to surrounding normal tissue.
LINAC radiation therapy may be used in the treatment of metastatic cancer or some benign brain tumors.
Stereotactic Radiation Therapy in the Treatment of Specific Types of Brain Tumors
Brain metastases: The addition of SRT to whole-brain radiation therapy (WBRT) appears to benefit patients thought to have only a single brain metastasis. A clinical study involving patients with one to three brain metastases was conducted to directly compare WBRT with or without SRS boost. Overall, the SRT boost appeared to improve survival only among patients who had a single metastasis.5
Outcomes with the addition of SRT to whole-brain radiation in the treatment of a single brain metastasis
|Whole-brain radiation therapy PLUS SRT boost||Whole-brain radiation therapy alone|
|Overall survival(1-2 metastases)||6.5 months||5.7 months|
|Survival for patients with 1 metastasis||16.5 months||4.9 months|
Research also indicates that SRT may be as effective as surgery for the treatment of some patients with brain metastases. A review of outcomes from patients with a single brain metastasis treated at the Mayo Clinic indicates that 56% of patients who received SRT and 62% patients treated with surgery lived one year or more after treatment, a difference that was not statistically significant. Furthermore, tumor control was better for the patients treated with SRT. None of the patients who received SRT had local recurrence of cancer, compared to 58% patients treated with surgery.6
Glioblastoma multiforme: Researchers from the Radiation Therapy Oncology Group have reported that the addition of SRT to conventional EBRT and chemotherapy does not appear to improve outcomes in patients with glioblastoma multiforme. There were 203 patients with brain tumors greater than or equal to 44 mm in diameter involved in this clinical trial. Patients were randomly assigned to receive conventional EBRT, chemotherapy, and SRT, or conventional EBRT and chemotherapy alone. Patients in both groups survived slightly more than a year: 13.6 months for patients who received the additional SRT and 13.5 months for patients who received only EBRT and chemotherapy. SRT did not appear to improve quality of life or mental functioning.7
While these results from SRT as “boost” therapy did not show an improvement over conventional treatment, research is ongoing to determine if SRT may benefit patients with glioblastoma multiforme.
Pituitary tumors: The pituitary gland is a bean-sized organ that produces many hormones that affect other parts of the body. Cancer in the pituitary gland is typically treated with surgical removal and radiation therapy. However pituitary tumors may result in the over-production of one or several important hormones, and SRT may decrease dangerously high hormonal levels faster than conventional radiation. A review of 34 published studies including 1,567 patients with pituitary cancers that were treated with SRT indicated that tumor growth can be controlled in approximately 90% of cases.8
Meningiomas: Meningiomas arise from the layers of tissue that cover the brain and spinal cord, called meninges. Most meningiomas are benign, or non-cancerous, and slow-growing. When the tumor cannot be completely removed with surgery, it may be possible to control the size and growth with radiation therapy, allowing patients to live many years with residual tumor tissue. However, meningiomas that are not controlled may cause pressure on the brain or spinal cord and associated symptoms, such as pain and impaired function. Long-term (10-year) results of Gamma Knife radiation therapy conducted at the University of Pittsburgh indicate that tumor size was reduced in more than half of patients with meningiomas.9
Results of SRT for meningiomas cannot be detected on radiographic imaging immediately after treatment. Therefore, the effect of treatment may not be known for many years. Researchers are evaluating new techniques to more quickly determine the outcomes of treatment.
Internal Radiation Therapy (Brachytherapy)
Brachytherapy is the delivery of radiation therapy by placing radioactive material directly into or near the brain tumor. The radioactive material may also be called “implants” or “seeds.” While standard radiation aims rays at the tumor from outside the body, brachytherapy attacks the tumor from the inside. The advantages to internal delivery of radiation are:
- Reduced damage to normal tissue, and therefore, reduced side effects,
- More concentrated delivery of radiation to the area where the cancer is mostly likely to recur, and
- Reduced risk of damage to normal brain tissue makes brachytherapy an option for patients with recurrent tumors who have undergone radiation treatment for recurrent brain tumors and may not be able to tolerate additional EBRT.
Brachytherapy is used in the treatment of newly diagnosed or recurrent brain tumors. It may be administered as the primary radiation therapy or as a “boost” of additional radiation delivered before or following standard external beam radiation. For boost therapy to be effective, the brain tumor must be no more than 2 inches in diameter and accessible by surgery. Larger tumors may require surgery to reduce the size of the tumor before the radiation sources are implanted. Brachytherapy is a local therapy; it is not commonly used for widely spread or multiple tumors.
Implantation procedure: To implant radiation energy in the tumor, catheters (tubes) are placed into the tumor bed using surgical techniques that are directed by CT and MRI. The sources of radiation, usually in pellet form, are placed in the catheters. Depending on the isotopes used, the implant is removed either after a few days, after several months or is left in place permanently. Steroids are commonly used with this therapy to decrease brain swelling. In rare instances, implantation might be repeated. Brachytherapy implants are typically temporary and are removed once treatment is completed. In some cases, an implant may be permanent.
A possible complication associated with brachytherapy is the build-up of dead tissue. The radiation being emitted from the implant kills the cancer cells, and in some cases, this may cause dead cells to build up faster than the body can remove them. Large amounts of dead tumor cells can cause complications. Some patients will require follow-up surgery to remove the dead tissue.
GliaSite® radiation therapy system (RTS): The GliaSite RTS involves placing an inflatable balloon in the area of the brain tumor at the time of surgery. Low-dose-rate radiation is delivered through a catheter (tube) into the balloon. The GliaSite RTS offers the advantage of a shorter stay in the hospital; most patients who undergo traditional external beam radiation therapy remain hospitalized for six weeks, whereas patients who receive their radiation treatment with GliaSite may return home within a week. GliaSite is approved by the U.S. Food and Drug Administration (FDA) for the treatment of malignant brain tumors.
Three published clinical trials indicate that GliaSite is a safe treatment for high-grade gliomas and brain metastases and may increase survival in the treatment of recurrent gliomas compared to surgery alone or surgery plus internal chemotherapy.10,11
Results from a clinical trial of GliaSite that was carried out in nine institutions in the U.S. and involved 81 patients indicate that this procedure improves survival and does not appear to reduce patients’ quality of life. The patients in this trial lived, on average, more than three months (38 weeks) after implantation and they were free from cancer progression for approximately 19 weeks. The researchers estimated that approximately one-third of patients lived one year or more. These patients lived nearly twice as long as a similar groups of patients from another trial who only underwent surgery. Also, approximately one-third of the patients treated with GliaSite lived longer than a group that underwent surgery and the placement of internal Gliadel wafer chemotherapy.12
Permanent low-intensity brachytherapy: Two studies have failed to show a significant improvement in outcomes with high-intensity, temporary brachytherapy implants. However, researchers have investigated the use of low-intensity, permanent implants comprised of iodine 125 and found them to be safe. Results from a clinical trial involving 22 patients with astrocytomas treated with surgical placement of a permanent implant showed that patients lived an average of 64 weeks and 57% of patients lived one year or more.13
Treatment schedules: Radiation therapy often begins a week or two after surgery, or as soon as the surgical wound heals. Conventional EBRT is usually given in 30–40 doses over a six-week period, five days a week. Brachytherapy may be administered for only a few days, followed by removal of the radioactive “seed”, and stereotactic radiation therapy is typically conducted in one single session.
Follow-up examinations: Results of therapy might not be obvious for several months or longer. Tumor cells that have been damaged by radiation cannot reproduce normally and gradually die. The brain clears away the dead tumor cells, but this is a lengthy process. Scans taken immediately following therapy can be confusing because swelling and dead cells often appear larger than the original tumor, and can cause symptoms similar to the tumor. It takes a few months before scans show the full benefit of the radiation.
Re-treatment with radiation: Radiation kills normal cells as well as tumor cells. Since brain tissue cannot replace itself, the effects of radiation are cumulative, causing severe side effects beyond a certain degree of exposure to radiation. For this reason, re-treatment with conventional fractionated radiation is not often recommended. However, additional radiation is possible in selected circumstances, including:
- Location of the tumor and its relation to critical brain tissue,
- When the previous radiation was given,
- The amount of radiation originally given, and
- The type of tumor and the age of the patient.
Brachytherapy and stereotactic radiation therapy are frequently used for selected patients who may benefit from retreatment with radiation therapy. These patients typically have recurrent malignant gliomas or metastatic brain tumors and have previously undergone conventional EBRT.
For more information about radiation therapy procedures, go to What to Expect During Radiation Therapy.
Radiation therapy is commonly associated with some side effects. However, patients experience side effects at different rates and to different degrees. A dose that causes some discomfort in one patient may cause no side effects in another, and may be disabling to a third. Side effects of radiation therapy can be grouped into general and those pertaining to neurological, or brain function. General side effects may include:
- Hair loss
- Skin irritation
- Hearing problems
- Appetite changes
To learn more, go to Management and Treatment of Side Effects.
Neurological side effects
The major side effect of radiation for brain tumors is damage to normal brain tissues, which can lead to mild, moderate, or severe brain damage. Newer radiation therapy techniques can limit these effects, but may not always eliminate them. Neurological side effects may occur immediately after treatment, a few weeks to a few months after the completion of treatment, or they may occur months or years after treatment and persist as long-term effects.
Immediately after treatment: Acute reactions occur immediately after treatment and are caused by radiation-induced brain swelling (edema). Symptoms can mimic the symptoms of your brain tumor, like speech problems or muscle weakness or those of increased intracranial pressure, such as headache, nausea, or double vision. Acute side effects are usually temporary and may be relieved by corticosteroids such as dexamethasone. Often, steroids are prescribed to be taken during the entire treatment so that acute side-effects are avoided or minimized. The steroid dose is gradually reduced and discontinued when treatment is completed.
Weeks or months after treatment: So-called “early delayed” or sub-acute reactions commonly occur between one and three months after treatment. Symptoms include loss of appetite, sleepiness, lack of energy, and an increase in pre-existing neurological symptoms. Sub-acute reactions are thought to be due to temporary disruption to the nerve coverings. These symptoms are usually temporary, lasting about six weeks, the length of time it takes for myelin to repair itself. In some cases, however, recovery may take several months.
Another reaction that can occur weeks or months after treatment is swelling as a result of the build-up of dead tumor cells. The brain lacks an effective lymph system, the clean-up system of the body. Therefore, dead tumor cells are cleared away very slowly and radiation-induced cell death may cause rapid build-up of dead cells. The swelling that occurs as a result of the dead cells may cause an increase in neurological symptoms similar to the symptoms of the brain tumor.
Months or years after treatment: Long-term effects occur as a result of changes in the white matter of the brain and death of brain tissue caused by radiation-damaged blood vessels. Symptoms can occur months to years after therapy is completed. These long-term effects are permanent and can be progressive. Symptoms vary from mild to severe and include: decreased intellect, memory impairment, confusion, personality changes, and alteration of the normal function of the area irradiated.
Long-term effects of radiation therapy are difficult to distinguish from new tumor growth. CT and MRI scans are not accurate and PET scanning might be helpful, but is not totally accurate either. It might be necessary to conduct a biopsy of the area to determine if a patient has new tumor growth.
One of the major, long-term side effects of radiation therapy is the development of a second cancer, frequently in the head and neck area. This often takes years to develop.
The development of more effective cancer treatments requires that new and innovative therapies be evaluated with cancer patients. Clinical trials are studies that evaluate the effectiveness of new treatment strategies. Future progress in radiation treatment for brain tumors will result from the continued evaluation of new treatments in clinical trials. Participation in a clinical trial may offer patients access to better treatments and advance the existing knowledge about treatment of this cancer. Patients who are interested in participating in a clinical trial should discuss the risks and benefits of clinical trials with their physician. Areas of active investigation aimed at improving the radiation treatment of brain tumors include the following:
- Combination therapy
- Intensity modulated radiation therapy (tomotherapy)
- Radioactive monoclonal antibodies
- Intraoperative radiation therapy
- Boron Neutron Capture Therapy (BNCT)
Combination Therapy: Combining 2 or more treatment modalities often provides the best opportunity to prolong an individual’s survival. Recent clinical studies have demonstrated that in selected patients with anaplastic glioma the combination of radiation followed by Temador (temozolomide) chemotherapy improves outcomes compared to treatment with radiation therapy alone. The CATON study revealed that Five-year overall survival was improved with adjuvant Temador given after radiation therapy but not during radiation therapy.14
Intensity modulated radiation therapy (IMRT): IMRT is an advanced form of 3-D conformal radiation therapy. IMRT, also called tomotherapy, delivers varying intensity of radiation with a rotating device. IMRT is similar to computed tomography (CT) scanning. In CT, a beam rotates around the patient, creating a sequence of cross-sectional images. IMRT also uses a rotating beam, except the beam delivers radiation. And like CT, IMRT delivers treatment one cross-section at a time.
The intensity of radiation that is delivered with IMRT is varied by the placement of “leaves” between the patient and the radiation delivery device, which either block or allow the passage of radiation. Rotating the radiation delivery around the patient allows for more specific targeting of the cancer. In conventional radiation therapy, the beam is usually delivered from several different directions, possibly five to 10. The greater the number of beam directions, the more the dose will be confined to the target cancer cells, sparing normal cells from exposure. IMRT delivers radiation from every point on a helix, or spiral, in contrast to only a few points.
Research indicates that IMRT is a viable treatment option for brain tumors, but preliminary results have not shown an increase in survival with this radiation therapy technique. In a clinical trial, 25 patients with glioblastoma multiforme were treated with surgery followed by IMRT. Patients survived an average of 9.5 months and were free from cancer progression for 5.2 months. Approximately 40% of patients lived one year or more.15
Radioactive monoclonal antibodies: Monoclonal antibodies are targeted therapies that can locate cancer in the body based on unique proteins (antigens) present on the surface of some cancer cell. A radioactive material, such as iodine 131, may be attached to the monoclonal antibody. The result is a treatment in which the antibody acts as the homing device to the cancer and the radioactive iodine 131 kills the cancer cells.
When used in the treatment of brain tumors, radioactive monoclonal antibodies are usually injected directly into the tumor tissue that remains after surgery or implanted into the tumor bed (the space left after the tumor is removed). Administration occurs over the course of several days. This procedure appears to be associated with fewer side effects than brachytherapy or stereotactic radiosurgery. Another important advantage to radioactive monoclonal antibodies is this treatment approach appears to produce substantially fewer dead cells, reducing the need for additional surgery to remove the dead tissue.16,17
Intraoperative radiotherapy (IORT): Intraoperative radiotherapy is a technique for delivering a large, single dose of radiation directly to the tumor at the time of surgery. Conducting radiation therapy during surgery provides the advantage of decreasing the damage to normal brain tissue. While research has not shown IORT to improve survival over conventional EBRT, outcomes are not worse with IORT. A clinical trial involving patients with malignant gliomas showed no significant difference in survival between the 32 patients who received IORT and a similar group of patients who underwent EBRT.18
Outcomes for patients undergoing intraoperative radiotherapy (IORT) and conventional EBRT
Boron Neutron Capture Therapy (BNCT): BNCT combines a special form of radiation with a drug that concentrates in tumor cells. The drug, which is a compound of the element boron, “captures” radiation energy, becomes unstable, and disintegrates. In this process, cell-killing radiation is emitted. Normal tissue is spared because the drug accumulates in cancer cells to a greater degree than in normal brain tissue and the radiation is harmless unless it reacts with the boron.
Initial research with this form of treatment began more than 30 years ago, but it was not possible to administer it until advanced radiation beam technology was developed. Research with BNCT is aimed at finding suitable boron compounds that do not have harmful side effects and are capable of concentrating only in tumor cells. Currently, research is ongoing around the world, but findings are still in their early stages.
In Japan, 183 patients with different kinds of brain tumors have been treated with BNCT since 1968.19 Initial results from clinical trials that are ongoing in Sweden indicate that BNCT is feasible in the treatment of glioblastoma multiforme. Seventeen patients have undergone treatment and researchers report that there have not been any BNCT-related side effects.20 This study is ongoing and final results will indicate whether the treatment was effective.
BNCT was found to be safe in a clinical trial conducted at the Brookhaven National Laboratory in Upton , New York . In this trial, 53 patients with glioblastoma multiforme were treated with BNCT. Patients who received the highest doses of radiation to the brain experienced some side effects, especially somnolence, or an inclination to sleep. Radiation dose did not appear to affect survival; rather the aggressiveness of therapy for recurrence impacted survival to a greater degree than radiation dose.21 Clinical trials of BCNU for glioblastomas are ongoing in a limited number of medical centers in the U.S.
Hyperthermia: Hyperthermia is heat therapy. The goal of this treatment technique is to heat the area where the cancer is to make the cancer cells more vulnerable to the effects of the cancer treatment. Cancer cells tend to be more sensitive to heat due to poor blood flow, decreased levels of oxygen, and an acidic environment. The procedure for hyperthermia involves careful and uniform administration of heat to the tumor while preventing contact with, and potential damage to, normal cells. Techniques used to heat the tissue involve directing different types of energy waves toward the cancer, such as radiofrequency waves, microwaves, and ultrasound. Researchers are working to determine the most effective way to deliver hyperthermia for the treatment of brain tumors.
A clinical trial that evaluated the addition of hyperthermia (“heat”) to brachytherapy found that the patients who received heat lived significantly longer and were free from cancer progression longer than patients who didn’t receive heat. All patients involved in this trial were initially treated with partial brain radiation therapy. Patients whose tumor was still implantable after the initial treatment were randomly assigned to receive brachytherapy boost with hyperthermia for 30 minutes immediately before and after brachytherapy (40 patients) or brachytherapy alone (39 patients). Of the patients who were randomized, outcomes were better for patients who were treated with hyperthermia.22
Outcomes for patients undergoing brachytherapy with or without hyperthermia
|Brachytherapy plus hyperthermia (n=35)||Brachytherapy alone(n=33)|
|Median survival||85 weeks||76 weeks|
2 Chan JL, Lee SW, Fraass BA, et al. Survival and failure patterns of high-grade gliomas after three-dimensional conformal radiotherapy. Journal of Clinical Oncology. 2002;20(6):1635-42.
3 Tanaka M, Ino Y, Nakagawa K, Tago M, Todo T. High-dose Conformation Radiotherapy for Supratentorial Malignant Glioma: A Historical Comparison. Lancet Oncology. 2005; 6: 953-960.
4 Weber DC, Lomax AJ, Rutz HP, et al. Spot-scanning proton radiation therapy for recurrent, residual and untreated intracranial meningiomas. Radiotherapy Oncology. 2004;71(3):247-9.
5 Andrews DW, Scott CB, Sperduto PW, et al. Whoel brain radiation therapy with or without stereotactic radiosurgery boost for patients with one to three brain metastases: phase III results of the RTOG 9508 randomised trial. Lancet. 2004;363:1665-1672.
6 O’Neill BP, Iturria NJ, Link MJ, et al. A comparison of surgical resection and stereotactic radiosurgery in the treatment of solitary brain metastases. International Journal of Radiation Oncology Biology Physics. 2003;55(5):1169-1176.
7 Souhami L, Seiferheld W, Brachman D, et al. Radomized comparison of stereotactic radiosurgery followed by conventional radiotherapy with carmustine to conventional radiotherapy with carmustine for patients with glioblastoma multiforme: report of Radiation Therapy Oncology Group-93-05 protocol. International Journal of Radiation Oncology Biology Physics. 2004;60(3):853-60.
8 Laws ER, Sheehan JP, Sheehan JM, et al. Stereotactic radiosurgery for pituitary adenomas: a review of the literature. Neurooncology. 2004;69(1-3):257-72
9 Kondziolka D, Nathooo N, Flickinger JC, et al. Long-term results after radiosurgery for benign intracranial tumors. Journal of Neurosurgery. 2003; 53:815-821.
10 Tatter SB, Shaw EG, Rosenblum ML, et al. An inflatable balloon catheter and liquid 125I radiation source (GliaSite Radiation Therapy System) for treatment of recurrent malignant glioma: multicenter safety and feasibility trial. Journal of Neurosurgery. 2003;99(2):297-303.
11 Rogers L, Shaw E, Rock JP, et al. Interim Results of A Phase II Study of Resection and GliaSite Brachytherapy for a Single Brain metasesis. Proceedings from the 46th annual meeting of the American Society of Radiology and Oncology held in Atlanta GA , October 2004; Abstract #1005.
12 Gabayan A, Sanan A, Bastin K, et al. Gliasite Radiotherapy System for Treatment of Recurrent Malignant Glioma: A Multi-Institutional Analysis. Proceedings from the 46th Annual Meeting of the American Society of Therapeutic Radiology and Oncology, held in Atlanta GA , October 2004. Abstract #1002.
13 Halligan JB, Selzer KJ, Rostomily RC, et al. Operation and permanent low activity 125I brachytherapy for recurrent high-grade astrocytomas. International Journal of Radiation Oncology, Biology, Physics. 1996;35:541-547.
14 2016 American Society of Clinical Oncology (ASCO) Annual Meeting (Abstract LBA2000).
15 Sultanem K, Patrocinio H, Lambert C, et al. The use of hypofractionated intensity-modulated irradiation in the treatment of glioblastoma multiforme: preliminary results of a prospective trial. International Journal of Radiation Oncology Biology Physics. 2004;58(1):247-52.
16 Reardon D, Akabani G, Coleman R, et al. Salvage Radioimmunotherapy With Murine Iodine-131–Labeled Antitenascin Monoclonal Antibody 81C6 for Patients With Recurrent Primary and Metastatic Malignant Brain Tumors: Phase II Study Results. Journal of Clinical Oncology. 2005; 24: 115-122.
17 C Grana, M Chinol, C Robertson, et al. Pretargeted adjuvant radioimmunotherapy with Yttrium-90-biotin in malignant glioma patients: A pilot study. British Journal of Cancer. 2002;86:207-212.
18 Nemoto K, Ogawa Y, Matsushita, H, et al. Intraoperative radiation therapy (IORT) for previously untreated malignant gliomas. BMC Cancer. 2002;2:1.
19 Nakgawa Y, Pooh K, Kobayashi T, et al. Clinical review of the Japanese experience with boron neutron capture therapy and a proposed strategy using epithermal neutron beams. Journal of Neurooncology. 2003;62:87-99.
20 Capala J, Stenstam BH, Skold K, et al. Boron Neutron Capture Therapy for Glioblastoma Multiforme: Clinical Studies in Sweden . Journal of Neurooncology. 2003;62:135-144.
21 Diaz AZ. Assessment of the results from the Phase I/II boron neutron capture therapy trials at the Brookhaven National Laboratory from a clinician’s point of view. Journal of Neurooncology. 2003;62:101-109.
22 Sneed PK , Stauffer PR, McDermott MW, et al. Survival benefit of hyperthermia in a prospective randomized trial of brachytherapy boost +/- hyperthermia for glioblastoma multiforme. International Journal of Radiation Oncology, Biology, Physics. 1998;40(2):287-95.
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