| Eligibility |
Inclusion Criteria:
1. Voluntary written consent must be given before performance of any study-related
procedure that is not part of standard medical care, with the understanding that
consent may be withdrawn by the subject at any time without prejudice to future
medical care.
2. Female or male subjects = 18 years old at the time of informed consent.
3. Histologically confirmed new diagnosis of GBM according to updated World Health
Organization (WHO) classification criteria.
4. Supratentorial tumor location.
5. Recovered from maximal debulking surgery, if applicable (gross total resection,
partial resection and biopsy-only patients are all acceptable).
6. Planned for standard adjuvant chemoradiotherapy of approximately 60 Gy of radiation
therapy (RT) , or biologically equivalent dose, according to local practice, and
concomitant TMZ chemotherapy (75 mg/m^2 daily) Any other cytotoxic or biologic
antitumor therapy received prior to enrollment will be considered an exclusion.
7. Planned treatment with adjuvant/maintenance TMZ (150 to 200 mg/m^2 daily x 5 d, q 28
days).
8. All patients with sufficient tissue must have had tissue submitted for
O6-Methylguanine-DNA Methyltransferase (MGMT) promoter methylation determination prior
to enrollment.
9. Karnofsky Performance Status Scale = 70.
10. Life expectancy greater than at least three months.
11. Study start date at least three weeks out from brain surgery.
12. Stable or decreasing dose of corticosteroids for the last seven days prior to
enrollment, if applicable.
13. Complete blood count (CBC) /differential obtained within 28 days prior to
registration, with adequate bone marrow function defined as follows: absolute
neutrophil count (ANC) = 1,500 cells/mm^3; platelets = 100,000 cells/mm^3; hemoglobin
= 10.0 g/dL. (Note: the use of transfusion or other intervention to achieve Hgb =10.0
g/dL is acceptable.)
14. Female subjects who:
1. Are postmenopausal for at least one year before the screening visit, OR
2. Are surgically sterile, OR
If they are of childbearing potential:
i. Agree to practice one highly effective method and one additional effective
(barrier) method of contraception, at the same time, from the time of signing the
informed consent through four months after the last study intervention (female and
male condoms should not be used together), OR ii. Agree to practice true abstinence,
when this is in line with the preferred and usual lifestyle of the subject. (Periodic
abstinence [e.g., calendar, ovulation, symptothermal, postovulation methods]
withdrawal, spermicides only, and lactational amenorrhea are not acceptable methods of
contraception.)
15. Male subjects, even if surgically sterilized (i.e., status postvasectomy), who:
1. Agree to practice effective barrier contraception during the entire study
treatment period from the time of signing the informed consent through four
months after the last study intervention (female and male condoms should not be
used together), OR
2. Agree to practice true abstinence, when this is in line with the preferred and
usual lifestyle of the subject. (Periodic abstinence [e.g., calendar, ovulation,
symptothermal, postovulation methods for the female partner] withdrawal,
spermicides only, and lactational amenorrhea are not acceptable methods of
contraception.)
Exclusion Criteria:
1. Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free
for a minimum of three years. (For example, carcinoma in situ of the breast, oral
cavity, or cervix are all permissible).
2. Recurrent or multifocal malignant gliomas.
3. Any site of distant disease (i.e., leptomeningeal disease or drop metastases from the
GBM tumor site).
4. Prior radiotherapy to the head or neck (except for T1 glottic cancer), resulting in
overlap of radiation fields.
5. Severe, active comorbidity, defined as follows:
- Unstable angina at registration.
- Transmural myocardial infarction within the last six months prior to
registration.
- Evidence of recent myocardial infarction or ischemia by the findings of S-T
elevations of = 2 mm using the analysis of an EKG performed within 28 days prior
to registration. (Note: EKG to be performed only if clinical suspicion of cardiac
issue.)
- New York Heart Association grade II or greater congestive heart failure requiring
hospitalization within 12 months prior to.
- Active connective tissue disorders, such as lupus or scleroderma, that in the
opinion of the treating physician may put the patient at high risk for radiation
toxicity.
- New York Heart Association grade II or greater congestive heart failure requiring
hospitalization within 12 months prior to registration.
- Active connective tissue disorders, such as lupus or scleroderma, that in the
opinion of the treating physician may put the patient at high risk for radiation
toxicity.
- End-stage renal disease (i.e., on dialysis or dialysis has been recommended).
6. Pregnancy or women of childbearing potential and men who are sexually active and not
willing/able to use medically acceptable forms of contraception; this exclusion is
necessary because the treatment involved in this study may be significantly
teratogenic.
7. Patents treated on any other therapeutic clinical protocols within 30 days prior to
registration.
8. Inability to undergo MRI.
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