Glioblastomas, the most frequent malignant brain tumor in adults, are widespread in the
brain, despite their discrete appearance on computed tomography (CT) or magnetic resonance
imaging (MRI). While this tumor tends to spread widely in the brain, unlike other tumors of
the body, it rarely metastasizes, or spreads, to other organs. Approximately 10 percent of
patients with glioblastoma develop metastatic disease after radiation or brain surgery. In
the absence of radiation or brain surgery, few patients have developed disease spread
outside the brain.
During surgery to remove tumors of other organs of the body, such as the lung, prostate,
kidney, or ovary, cells from these tumors are routinely found in the bloodstream. These
cells are believed to be the reason for the spread of these tumors. In the case of
malignant brain tumors, this process of glioma (tumor) cells shedding into circulation has
not yet been investigated.
This study will determine whether glioma cells can be detected in the bloodstream of
patients undergoing surgery. If glioma cells are absent, it may mean they are unable to
penetrate the blood-brain barrier. If they are present, they presumably can penetrate into
blood vessels but they may be recognized and eliminated by the immune system, or they may
escape detection yet not be able to take hold in the new microenvironment. The results of
the study will add to the knowledge of the biology of these highly malignant tumors.
Study participants will be admitted to the hospital for 8 to 10 days. They will undergo a
complete physical and neurological exam and blood and urine tests. An electrocardiogram
will be performed, and x-rays may be taken. On the morning of surgery, the patient will
receive sedation intravenously. A tiny plastic tube called a catheter will be introduced
into a vein in the groin through needles. The catheter will be passed through to the
jugular bulb, right above the jugular vein, on the same side as the tumor. The patient will
then be taken to the operating room for surgery. During surgery, not more than one quarter
of a unit of blood will be removed through the catheter. The catheter will be removed
before the patient enters the intensive care unit. Another MRI will be taken after surgery.
The study will enroll participants for 2 years. Patients will be followed at 3 months and 6
months after the surgery to make sure the postoperative period is uneventful.
Glioblastomas are the most frequent malignant brain tumor in adults and are widespread in
the brain despite their discrete appearance on CT or MRI. While locally aggressive,
metastasis of glioblastoma to extracranial organs is considered rare. Approximately 10% of
patients with glioblastoma develop metastatic disease after radiation or craniotomy. Few
patients have developed extracranial metastatic disease in the absence of surgical resection
or radiation. Unlike tumors of other organs such as lung, colon and prostate, the presence
of glioma cells in the circulation of patients undergoing surgical resection has not been
established. If found absent, glioma cells may be unable to intravasate through the blood
brain barrier. If present, these tumor cells presumably can intravasate but may be
recognized and eliminated by an immunological process, or they may escape detection yet not
be able to take hold in the new microenvironment. The information provided will add to the
knowledge of the biology of these highly malignant tumors.
Patients must be diagnosed with biopsy-proven glioblastoma multiforme or anaplastic
astrocytoma (WHO grade III and IV, WHO classification of glial tumors) and meet the
Consenting males and females between the ages of 18 and 75, inclusive.
Provided written informed consent prior to participation in the trial.
Karnofsky Performance Scale Score greater than or equal to 60.
Patients of all races and sexes are eligible for this study. Children and adolescents
only rarely are afflicted with gliomas that are amenable for surgical resection, and so
are excluded from this study.
Patients who have been accepted for glioma resection under existing NINDS protocols are
also eligible for this study.
If tumor tissue is available from biopsy prior to surgery, we will attempt to identify
tumor-specific mutation(s) prior to enrolling the patient.
Clinically unstable condition.
Liver function impairment (total bilirubin greater than 2.0 mg/dl; AST or ALT greater than
3 times the upper limit of normal).
Coagulopathy (prothrombin time [PT] or activated partial thromboplastin time [APTT] > 1.5
Thrombocytopenia (platelet count less than 100,000/mm3).
Granulocytopenia (absolute neutrophil count less than 1,000/mm3).
Acute medical problems.
Positive HIV test.
Karnofsky Performance Scale Score less than 60.
Allergy to CT contrast agents.
Absence of tumor-specific gene mutation.
Pregnant women. Women of child-bearing potential will undergo a urine and/or serum
pregnancy test. Women who are pregnant will not be allowed to participate in this study.