A Dose Per Fraction Escalation Trial of Hypofractionated IMRT With Temozolomide for Newly Diagnosed Glioblastoma

Hypo-IMRT is given in fewer treatments than conventional radiation therapy. This will be a
dose per fraction escalation study. A dose per fraction escalation study means that
successive groups of patients will receive higher doses per fraction of radiation while
keeping the total dose of radiation the same (60 Gy, Gy is a radiation unit). The radiation
dose per fraction will be increased and the numbers of radiation treatments will be
decreased until a fraction dose is reached at which there are unacceptable side effects
compared with possible benefit. Which group subjects are assigned to will depend on what
stage the study has reached at the time the subject decide to participate.

This research is being done because with current standard radiation therapy (A total dose of
60 Gy given 2 Gy a day over 6 weeks) the outcome is very poor. New and more effective
radiation therapy methods are desperately needed for patients with GBM.

In this study, radiation therapy is given together with chemotherapy of Temozolomide.

This study is also designed to monitor the level of some of the known cytokines (specific
proteins in the blood) before and after radiation, and in meantime to screen unknown
proteins in patients' blood before and after radiation therapy. Hopefully, this will provide
some clues for future study of monitoring radiation damage, and possibly new therapeutic
approach for patients with GBM.

Inclusion Criteria:

- Histopathologically confirmed WHO grade IV astrocytoma (GBM), tumor can be supra- or
infra-tentorial in location but not located in the brain stem.

- Solitary or multifocal tumor.

- Tumor can be biopsied or resected, either totally or sub-totally.

- A pre-radiation therapy brain MRI is mandatory.

- Surgical cavity or surgical cavity + T1 enhancing residual tumor ≤ 6 cm in the
largest diameter on the pre-radiation therapy MRI. In the case of multifocal tumor,
the combined largest diameter of T1 enhancing tumor + surgical cavity ≤ 6 cm.

- Placement of bis-chloronitrosourea (BCNU) wafers at the time of surgery is allowed.

- Age > 18 years at time of registration.

- Estimated survival of at least 3 months.

- Zubrod Performance Scale of 0-2 (Karnofsky performance scale ≥ 60).

- Hgb > 9 gm; absolute neutrophil count (ANC) > 1500/ul; platelets > 100,000;
Creatinine < 1.5 times the upper limit of laboratory normal value; Bilirubin < 2
times the upper limit of laboratory normal value; serum glutamate pyruvate
transaminase (SGPT) or serum glutamate oxaloacetate transaminase (SGOT) < 3 times the
upper limit of laboratory normal value.

- Patients must sign study-specific informed consent form prior to registration.

- Men and women and members of all ethnic groups are eligible for this trial.

- Radiation therapy and chemotherapy must start within 8 weeks of tumor resection or
biopsy

Exclusion Criteria:

- Patients with contraindications for MRI scanning.

- Prior temozolomide chemotherapy.

- Prior brain irradiation.

- Evidence of severe or uncontrolled psychiatric or systemic disease (e.g., unstable or
uncompensated respiratory, cardiac, hepatic, or renal disease) that would interfere
with study protocol as judged by the investigator.

- Acquired Immune Deficiency (HIV (+)/AIDS)

- Patients being treated on any other clinical protocols within 30 days prior to study
entry or during participation in the study.

- Pregnant women or breast feeding women. Women of childbearing potential must practice
medically approved contraceptive precautions. Men should be counseled and agreeable
to follow acceptable birth control methods.

- Active connective tissue disorders, such as active lupus or scleroderma.

- Concurrent active malignancy at other sites.

- Frequent vomiting of medical condition which could interfere with oral medication
intake (e.g. partial bowel obstruction).