A glioma is a kind of brain tumor that originates from glial
cells, which support and nourish neurons in the brain. Gliomas account for
about 25 percent of childhood cancers, and most gliomas are both highly
treatable and highly curable. The most common kind of glioma, called a
pilocytic astrocytoma, has a cure rate over 90 percent.
Gliomas are divided into four grades, depending on the tumor
cells' appearance under a microscope; the higher a tumor's grade number, the
more severe it is. Grades 1 and 2 are considered low-grade gliomas and account
for about two-thirds of all pediatric tumors. Grades 3 and 4 are considered
high-grade gliomas.
Gliomas can also be classified based on their location and
by the kind of glial cell—astrocytes, oligodendrocytes, or ependymocytes—from
which they arise.
Children and adolescents with glioma are treated at
Dana-Farber/Boston Children’s through the Brain Tumor Center's Glioma Program,
one of the largest and most experienced pediatric glioma programs in the world.
Our glioma specialists—a team of neuro-oncologists,
surgeons, pathologists, and radiation oncologists—focus solely on the care of
children diagnosed with gliomas. The Glioma Program also offers families the
chance to have
their child's tumor molecularly profiled (as
long as a biopsy can be taken), which may help identify opportunities for
targeted treatment.
As a glioma grows, it presses on surrounding healthy parts
of the brain, affecting their function. As such, the symptoms of a pediatric
glioma depend heavily on the tumor's size and where in the brain it is located.
Some of the most common symptoms of a pediatric glioma include:
- headache, particularly in the morning or made
better by vomiting
- severe or frequent vomiting without other signs
of gastrointestinal illness
- vision problems, such as double vision, blurry
vision, or loss of vision
- difficulty walking or balancing
- seizures
- weight gain or loss
- premature puberty
- clumsiness
- confusion
- sleepiness
- changes in behavior
To diagnose a pediatric glioma, your doctor will take your
child's medical history and carry out both physical and neurological exams.
Your doctor may also order a variety of tests, including:
- a magnetic resonance
imaging (MRI) scan to evaluate the tumor and determine its extent
- biopsy or
tissue sample from the tumor to provide definitive information about the type
of tumor and its grade and allow for molecular profiling of tumor cells
- electroencephalogram (EEG), which measures the
brain's electrical activity
- lumbar puncture, in which a doctor takes a small
sample of cerebrospinal fluid from near the base of the spine to see whether
the tumor has spread
Specific glioma diagnoses include:
After all tests are
completed, doctors will be able to outline the best treatment options.
Our treatment approach for pediatric gliomas is personalized
for each patient depending on several factors, including the tumor's type,
stage, and location. Some therapies will treat the tumor, while others are
intended to address complications of the disease or side effects of the
treatment.
In addition, our clinicians may offer access to targeted
treatments based
on the molecular profile of your child's tumor.
Some of the options your doctor may discuss include:
- surgery to remove as much of the tumor as
possible
- chemotherapy, either before surgery to shrink
the tumor or after surgery to eliminate any remaining tumor cells
- radiation therapy to eliminate any remaining
tumor cells after surgery or to treat tumors that cannot be treated surgically
(a.k.a. unrescetable tumors). The use of radiation is determined by the type of
glioma. It is used commonly for children with high-grade gliomas. However, we
avoid using radiation whenever possible in children with low-grade gliomas to
avoid possible
long-term side effects.
We also offer innovative clinical trials for
children with glioma. Some have been launched by our own physicians, while
others are available through our participation in collaborative groups such as the
Children's
Oncology Group (COG) and the Pacific Pediatric Neuro-Oncology Consortium (PNOC).
Should you have questions or need advice on whether a
particular trial would be appropriate for your child, email our clinical trials
team at clinicaltrials@danafarberbostonchildrens.org.
We can help you navigate your options.
Your child’s prognosis (chance of recovery) and treatment
options depend on a number of different factors, including:
- type of tumor
- tumor grade
-
the extent of the disease
- the size and location of the tumor
- the presence or absence of metastasis
- the tumor's response to therapy
- the age and overall health of your child
- your child's tolerance of specific medications,
procedures, or therapies
- new developments in treatment
In general, low-grade
gliomas tend to be more treatable, while high-grade gliomas are more difficult
to treat and require more aggressive therapy. Prompt medical attention and
appropriate therapy are important for the best prognosis.
Many brain tumor survivors face physical, psychological,
social, and intellectual challenges related to their treatment and will require
ongoing assessment and specialized care.
To address the needs of this growing community of brain
tumor survivors, Dana-Farber/Boston Children's established the Stop &
Shop Family Pediatric Neuro-Oncology Outcomes Clinic.
This multi-disciplinary program addresses long-term health and social issues
for families and survivors of childhood brain tumors.
Today, the Outcomes Clinic follows more than 1,000 pediatric
brain tumor survivors of all ages, providing such services as:
- MRI scans to monitor for tumor recurrences
- intellectual function evaluation
- endocrine evaluation and treatment
- neurologic assessment
- psychosocial care
- hearing, vision monitoring
- ovarian dysfunction evaluation and treatment
- motor function evaluation and physical therapy
- complementary medicine
As a result of treatment, children may experience changes in
intellectual and motor function. Several programs address these needs, among
them the School
Liaison and Back-to-School programs,
which provide individualized services to ease a child's return to school and
maximize his ability to learn. In addition to providing thorough and
compassionate care, Outcomes Clinic specialists conduct innovative survivorship
research and provide continuing education for staff, patients, and families.
Research is a top priority at Dana-Farber/Boston Children's,
and our physicians work continuously to translate laboratory findings into
clinical therapies and find ways to improve survival while reducing the
toxicity and long-term impact of treatment.
For instance, a 2014 study led by Peter Manley, MD,
documented the excellent long-term survival among patients with low-grade
gliomas and the
negative impact of radiation therapy—long
a mainstay of pediatric brain tumor treatment—on that survival.
The Glioma Program's research enterprise mirrors its
clinical efforts in its multidisciplinary nature. Basic, translational, and
clinical scientists in the program work together and with colleagues at
institutions like the Broad Institute to
uncover new knowledge about the biology of gliomas and translate that
understanding into new therapies or ways of overcoming resistance to existing
ones.
Dana-Farber/Boston Children's houses the Pediatric
Low-Grade Astrocytoma (PLGA) Program, the world's only multidisciplinary clinical and research program dedicated to
pediatric low-grade gliomas. Established in 2007 with support from the PLGA
Foundation, the program takes a multifaceted approach to finding more
effective, less toxic treatments and a cure for children battling brain tumors,
and has become the standard bearer for the research and care of pediatric brain
tumors. Our pediatric neuro-oncologists, including Pratiti
(Mimi) Bandopadhayay, MBBS, PhD,
are actively contributing to these efforts.
It’s possible that your child will be eligible to
participate in one of the Glioma Program’s current clinical trials.
In addition to launching our own clinical trials, we also offer trials available through collaborative groups such as the Children's
Oncology Group (COG) and the Pacific Pediatric Neuro-Oncology Consortium (PNOC).